Item | Value |
---|---|
geneid | 80816 |
ensemblid | ENSG00000141431.14 |
hgncid | 29357 |
symbol | ASXL3 |
name | ASXL transcriptional regulator 3 |
refseq_nuc | NM_030632.3 |
refseq_prot | NP_085135.1 |
ensembl_nuc | ENST00000269197.12 |
ensembl_prot | ENSP00000269197.4 |
mane_status | MANE Select |
chr | chr18 |
start | 33578219 |
end | 33751195 |
strand | + |
ver | v1.2 |
region | chr18:33578219-33751195 |
region5000 | chr18:33573219-33756195 |
regionname0 | ASXL3_chr18_33578219_33751195 |
regionname5000 | ASXL3_chr18_33573219_33756195 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2248 | 137 | 50 | 22 | 45 | 2 | 17 | 36 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0002 | 1/0 | 2248 | 50 | 12 | 14 | 10 | 4 | 9 | 7 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0003 | 0/0 | 2248 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0004 | 0/0 | 2248 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0005 | 0/0 | 2248 | 4 | 1 | 1 | 1 | 0 | 1 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0006 | 0/0 | 2248 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0007 | 0/0 | 2248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0008 | 0/0 | 2248 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0009 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0010 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0011 | 0/0 | 2248 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0012 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0013 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0014 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0015 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
a0016 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | MKDKR others(2243): Show |
chr18 | 33573219 | 33756195 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 6744 | 124 | 47 | 21 | 37 | 2 | 16 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0005 | 0/0 | 6744 | 7 | 0 | 0 | 7 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0008 | 0/0 | 6744 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0016 | 0/0 | 6744 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0017 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0018 | 0/0 | 6744 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0001c0020 | 0/0 | 6744 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0002c0002 | 1/0 | 6744 | 42 | 5 | 14 | 9 | 4 | 9 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0002c0006 | 0/0 | 6744 | 7 | 7 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0002c0013 | 0/0 | 6744 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0003c0003 | 0/0 | 6744 | 8 | 8 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0004c0004 | 0/0 | 6744 | 7 | 6 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0005c0007 | 0/0 | 6744 | 3 | 0 | 1 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0005c0024 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0006c0010 | 0/0 | 6744 | 2 | 1 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0006c0025 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0007c0009 | 0/0 | 6744 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0008c0011 | 0/0 | 6744 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0009c0023 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0010c0014 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0011c0012 | 0/0 | 6744 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0012c0022 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0013c0015 | 0/0 | 6744 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0014c0021 | 0/0 | 6744 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0015c0026 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 | ||
a0016c0019 | 0/0 | 6744 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | ATGAA others(6739): Show |
chr18 | 33573219 | 33756195 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 11756 | 57 | 14 | 20 | 13 | 1 | 8 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0002 | 0/0 | 11761 | 23 | 6 | 0 | 12 | 0 | 5 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0005 | 0/0 | 11756 | 11 | 11 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0006 | 0/0 | 11755 | 7 | 0 | 0 | 7 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11750): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0008 | 0/0 | 11761 | 6 | 6 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0009 | 0/0 | 11760 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0010 | 0/0 | 11756 | 3 | 0 | 0 | 2 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0011 | 0/0 | 11758 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11753): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0012 | 0/0 | 11757 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11752): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0014 | 0/0 | 11761 | 2 | 0 | 0 | 0 | 1 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0018 | 0/0 | 11761 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0021 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0022 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0028 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0029 | 0/0 | 11755 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11750): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0030 | 0/0 | 11755 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11750): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0031 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0035 | 0/0 | 11764 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11759): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0039 | 0/0 | 11760 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0001c0001t0042 | 0/0 | 11758 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11753): Show |
chr18 | 33573219 | 33756195 |
a0001c0005t0002 | 0/0 | 11761 | 6 | 0 | 0 | 6 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0005t0020 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0008t0017 | 0/0 | 11760 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0001c0008t0040 | 0/0 | 11760 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0001c0016t0045 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0001c0017t0038 | 0/0 | 11759 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0001c0018t0001 | 0/0 | 11756 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0001c0020t0001 | 0/0 | 11756 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0001 | 0/0 | 11756 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0003 | 1/0 | 11760 | 20 | 1 | 8 | 1 | 3 | 6 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0004 | 0/0 | 11761 | 16 | 4 | 3 | 7 | 0 | 2 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0019 | 0/0 | 11761 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0023 | 0/0 | 11760 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0024 | 0/0 | 11759 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0025 | 0/0 | 11760 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0002c0002t0046 | 0/0 | 11761 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0002c0006t0007 | 0/0 | 11759 | 6 | 6 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0002c0006t0043 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11757): Show |
chr18 | 33573219 | 33756195 |
a0002c0013t0027 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0003c0003t0009 | 0/0 | 11760 | 3 | 3 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0003c0003t0013 | 0/0 | 11760 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0003c0003t0016 | 0/0 | 11759 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0003c0003t0037 | 0/0 | 11759 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0003c0003t0044 | 0/0 | 11760 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0004c0004t0003 | 0/0 | 11760 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0004c0004t0004 | 0/0 | 11761 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0004c0004t0026 | 0/0 | 11773 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11768): Show |
chr18 | 33573219 | 33756195 |
a0005c0007t0001 | 0/0 | 11756 | 2 | 0 | 1 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0005c0007t0002 | 0/0 | 11761 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0005c0024t0005 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0006c0010t0015 | 0/0 | 11757 | 2 | 1 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11752): Show |
chr18 | 33573219 | 33756195 |
a0006c0025t0041 | 0/0 | 11758 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11753): Show |
chr18 | 33573219 | 33756195 |
a0007c0009t0002 | 0/0 | 11761 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0008c0011t0003 | 0/0 | 11760 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11755): Show |
chr18 | 33573219 | 33756195 |
a0009c0023t0032 | 0/0 | 11759 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11754): Show |
chr18 | 33573219 | 33756195 |
a0010c0014t0047 | 0/0 | 11761 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0011c0012t0001 | 0/0 | 11756 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0012c0022t0033 | 0/0 | 11757 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11752): Show |
chr18 | 33573219 | 33756195 |
a0013c0015t0001 | 0/0 | 11756 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0014c0021t0001 | 0/0 | 11756 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11751): Show |
chr18 | 33573219 | 33756195 |
a0015c0026t0036 | 0/0 | 11761 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
a0016c0019t0034 | 0/0 | 11761 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | AGAGT others(11756): Show |
chr18 | 33573219 | 33756195 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0014g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0018g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0022g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0028g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0029g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0030g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0035g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0039g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0042g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0020g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0008t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0008t0040g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0016t0045g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0017t0038g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0018t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0020t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0019g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0023g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0024g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0025g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0046g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0043g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0013t0027g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0044g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0026g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0024t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0010t0015g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0010t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0025t0041g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0007c0009t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0007c0009t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0008c0011t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0009c0023t0032g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0010c0014t0047g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0011c0012t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0012c0022t0033g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0013c0015t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0014c0021t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0015c0026t0036g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0016c0019t0034g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0025 | g0052 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0106 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0068 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00438 | hp2 | a0002 | c0013 | t0027 | g0079 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00558 | hp2 | a0001 | c0005 | t0002 | g0163 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00621 | hp2 | a0001 | c0005 | t0002 | g0165 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0078 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00673 | hp2 | a0002 | c0002 | t0004 | g0146 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00735 | hp2 | a0001 | c0001 | t0029 | g0164 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00741 | hp1 | a0002 | c0002 | t0004 | g0038 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0042 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01070 | hp2 | a0002 | c0002 | t0024 | g0133 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01071 | hp1 | a0004 | c0004 | t0003 | g0201 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0108 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01109 | hp2 | a0002 | c0002 | t0019 | g0178 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01192 | hp1 | a0002 | c0002 | t0046 | g0169 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01255 | hp2 | a0006 | c0010 | t0015 | g0168 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0114 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0144 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01361 | hp2 | a0002 | c0002 | t0004 | g0046 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01496 | hp2 | a0008 | c0011 | t0003 | g0218 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01891 | hp2 | a0004 | c0004 | t0004 | g0045 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0136 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01975 | hp2 | a0002 | c0002 | t0004 | g0080 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0063 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02055 | hp2 | a0002 | c0002 | t0004 | g0167 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02145 | hp2 | a0002 | c0006 | t0007 | g0036 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02257 | hp2 | a0003 | c0003 | t0009 | g0011 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02258 | hp1 | a0003 | c0003 | t0009 | g0172 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02300 | hp1 | a0001 | c0018 | t0001 | g0069 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02300 | hp2 | a0005 | c0007 | t0001 | g0107 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02523 | hp1 | a0002 | c0002 | t0004 | g0125 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02615 | hp1 | a0004 | c0004 | t0004 | g0176 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02622 | hp2 | a0004 | c0004 | t0004 | g0059 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02630 | hp1 | a0003 | c0003 | t0016 | g0019 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02647 | hp1 | a0002 | c0006 | t0007 | g0032 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02647 | hp2 | a0001 | c0001 | t0022 | g0073 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02723 | hp1 | a0002 | c0006 | t0007 | g0031 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02723 | hp2 | a0001 | c0008 | t0017 | g0025 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02818 | hp1 | a0009 | c0023 | t0032 | g0116 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02886 | hp1 | a0007 | c0009 | t0002 | g0158 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0028 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02895 | hp1 | a0001 | c0008 | t0040 | g0219 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02895 | hp2 | a0002 | c0006 | t0007 | g0030 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02896 | hp2 | a0001 | c0001 | t0030 | g0064 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02897 | hp2 | a0002 | c0006 | t0007 | g0029 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02965 | hp1 | a0003 | c0003 | t0013 | g0006 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02970 | hp1 | a0002 | c0006 | t0007 | g0026 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02976 | hp1 | a0004 | c0004 | t0004 | g0058 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03017 | hp1 | a0002 | c0002 | t0004 | g0128 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0192 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03098 | hp2 | a0003 | c0003 | t0009 | g0173 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0137 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03195 | hp2 | a0006 | c0025 | t0041 | g0005 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03209 | hp1 | a0001 | c0017 | t0038 | g0174 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03209 | hp2 | a0010 | c0014 | t0047 | g0004 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03225 | hp1 | a0007 | c0009 | t0002 | g0159 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03225 | hp2 | a0002 | c0006 | t0043 | g0101 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0132 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0135 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0181 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03486 | hp2 | a0003 | c0003 | t0044 | g0215 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03490 | hp2 | a0005 | c0007 | t0002 | g0134 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03516 | hp1 | a0004 | c0004 | t0004 | g0214 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03579 | hp1 | a0005 | c0024 | t0005 | g0027 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0142 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0056 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03704 | hp2 | a0001 | c0001 | t0014 | g0179 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03710 | hp1 | a0011 | c0012 | t0001 | g0039 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0111 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0153 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04199 | hp1 | a0002 | c0002 | t0004 | g0129 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0217 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04204 | hp2 | a0001 | c0020 | t0001 | g0154 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18906 | hp2 | a0002 | c0002 | t0004 | g0180 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18943 | hp1 | a0013 | c0015 | t0001 | g0115 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18970 | hp1 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18975 | hp2 | a0014 | c0021 | t0001 | g0071 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18982 | hp2 | a0005 | c0007 | t0001 | g0074 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0084 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18998 | hp1 | a0002 | c0002 | t0004 | g0193 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18998 | hp2 | a0001 | c0005 | t0002 | g0204 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18999 | hp1 | a0001 | c0001 | t0021 | g0088 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18999 | hp2 | a0001 | c0005 | t0020 | g0062 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19003 | hp2 | a0001 | c0001 | t0039 | g0102 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19010 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19010 | hp2 | a0002 | c0002 | t0004 | g0161 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19030 | hp1 | a0003 | c0003 | t0013 | g0010 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19030 | hp2 | a0015 | c0026 | t0036 | g0043 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19054 | hp1 | a0001 | c0001 | t0035 | g0098 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19054 | hp2 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19057 | hp1 | a0001 | c0005 | t0002 | g0061 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19065 | hp1 | a0002 | c0002 | t0023 | g0139 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19065 | hp2 | a0001 | c0005 | t0002 | g0162 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19074 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19076 | hp2 | a0001 | c0016 | t0045 | g0199 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19077 | hp1 | a0001 | c0001 | t0010 | g0195 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19077 | hp2 | a0002 | c0002 | t0004 | g0075 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19240 | hp1 | a0004 | c0004 | t0026 | g0057 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0143 | EUR | TSI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20752 | hp2 | a0001 | c0001 | t0014 | g0053 | EUR | TSI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02486 | hp1 | a0001 | c0001 | t0028 | g0189 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0120 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02559 | hp2 | a0001 | c0001 | t0031 | g0066 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0148 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03471 | hp2 | a0003 | c0003 | t0037 | g0009 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG06807 | hp1 | a0006 | c0010 | t0015 | g0184 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG06807 | hp2 | a0012 | c0022 | t0033 | g0118 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0109 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20300 | hp2 | a0016 | c0019 | t0034 | g0003 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA21309 | hp1 | a0001 | c0001 | t0042 | g0182 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0185 | REF | REF | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0096 | REF | REF | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33670709 | T | C | 1 | a0008 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.514T>C | p.Ser172Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/12 | 927/11760 | 514/6747 | 172/2248 | chr18 | 33670709 | |||
chr18:33738813 | A | C | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1409A>C | p.His470Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 1822/11760 | 1409/6747 | 470/2248 | chr18 | 33738813 | |||
chr18:33739983 | T | A | 2 | a0009 a0012 |
2 | HG02818.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.2579T>A | p.Met860Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2992/11760 | 2579/6747 | 860/2248 | chr18 | 33739983 | |||
chr18:33740135 | G | A | 1 | a0011 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.2731G>A | p.Val911Met | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 3144/11760 | 2731/6747 | 911/2248 | chr18 | 33740135 | |||
chr18:33740265 | A | G | 11 | a0001 a0003 a0004 others(8): Show |
162 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(159): Show |
missense_variant | MODERATE | c.2861A>G | p.Asn954Ser | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 3274/11760 | 2861/6747 | 954/2248 | chr18 | 33740265 | |||
chr18:33743777 | A | C | 1 | a0014 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.3929A>C | p.Glu1310Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4342/11760 | 3929/6747 | 1310/2248 | chr18 | 33743777 | |||
chr18:33743884 | A | G | 2 | a0006 a0007 |
5 | HG01255.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
missense_variant | MODERATE | c.4036A>G | p.Ile1346Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4449/11760 | 4036/6747 | 1346/2248 | chr18 | 33743884 | |||
chr18:33744088 | G | A | 1 | a0010 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.4240G>A | p.Ala1414Thr | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4653/11760 | 4240/6747 | 1414/2248 | chr18 | 33744088 | |||
chr18:33744092 | T | G | 1 | a0003 | 8 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
missense_variant | MODERATE | c.4244T>G | p.Met1415Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4657/11760 | 4244/6747 | 1415/2248 | chr18 | 33744092 | |||
chr18:33744113 | C | A | 1 | a0013 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.4265C>A | p.Thr1422Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4678/11760 | 4265/6747 | 1422/2248 | chr18 | 33744113 | |||
chr18:33744290 | T | C | 1 | a0012 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.4442T>C | p.Leu1481Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4855/11760 | 4442/6747 | 1481/2248 | chr18 | 33744290 | |||
chr18:33744506 | C | T | 1 | a0016 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.4658C>T | p.Pro1553Leu | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5071/11760 | 4658/6747 | 1553/2248 | chr18 | 33744506 | |||
chr18:33744970 | A | G | 9 | a0001 a0003 a0005 others(6): Show |
156 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(153): Show |
missense_variant | MODERATE | c.5122A>G | p.Met1708Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5535/11760 | 5122/6747 | 1708/2248 | chr18 | 33744970 | |||
chr18:33746207 | C | T | 1 | a0007 | 2 | HG02886.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.6359C>T | p.Ala2120Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6772/11760 | 6359/6747 | 2120/2248 | chr18 | 33746207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33739399 | A | G | 1 | a0006c0025 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1995A>G | p.Arg665Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2408/11760 | 1995/6747 | 665/2248 | chr18 | 33739399 | |||
chr18:33739711 | A | G | 1 | a0003c0003 | 8 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.2307A>G | p.Arg769Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2720/11760 | 2307/6747 | 769/2248 | chr18 | 33739711 | |||
chr18:33739915 | C | T | 4 | a0002c0006 a0005c0024 a0009c0023 others(1): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.2511C>T | p.Thr837Thr | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2924/11760 | 2511/6747 | 837/2248 | chr18 | 33739915 | |||
chr18:33739987 | A | T | 2 | a0009c0023 a0012c0022 |
2 | HG02818.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.2583A>T | p.Ile861Ile | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2996/11760 | 2583/6747 | 861/2248 | chr18 | 33739987 | |||
chr18:33743313 | G | A | 1 | a0001c0008 | 2 | HG02723.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.3465G>A | p.Ser1155Ser | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3878/11760 | 3465/6747 | 1155/2248 | chr18 | 33743313 | |||
chr18:33744087 | C | T | 1 | a0001c0020 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.4239C>T | p.Val1413Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4652/11760 | 4239/6747 | 1413/2248 | chr18 | 33744087 | |||
chr18:33744597 | A | G | 1 | a0015c0026 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.4749A>G | p.Ala1583Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5162/11760 | 4749/6747 | 1583/2248 | chr18 | 33744597 | |||
chr18:33744768 | G | A | 1 | a0002c0013 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.4920G>A | p.Lys1640Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5333/11760 | 4920/6747 | 1640/2248 | chr18 | 33744768 | |||
chr18:33744954 | A | G | 1 | a0001c0018 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.5106A>G | p.Val1702Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5519/11760 | 5106/6747 | 1702/2248 | chr18 | 33744954 | |||
chr18:33745779 | T | A | 1 | a0001c0016 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.5931T>A | p.Leu1977Leu | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6344/11760 | 5931/6747 | 1977/2248 | chr18 | 33745779 | |||
chr18:33745839 | A | G | 2 | a0001c0008 a0001c0017 |
3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.5991A>G | p.Lys1997Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6404/11760 | 5991/6747 | 1997/2248 | chr18 | 33745839 | |||
chr18:33746451 | C | T | 1 | a0001c0005 | 7 | HG00558.hp2 HG00621.hp2 NA18998.hp2 others(4): Show |
synonymous_variant | LOW | c.6603C>T | p.Ala2201Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 7016/11760 | 6603/6747 | 2201/2248 | chr18 | 33746451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33578269 | C | A | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0018 others(4): Show |
27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-363C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 363 | chr18 | 33578269 | ||||||
chr18:33578458 | C | CCCG | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0012 others(4): Show |
12 | HG01192.hp1 HG01433.hp2 HG01981.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-133dupGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCG | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(4): Show |
13 | HG02109.hp1 HG02129.hp1 HG02145.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-138_-133dupGCCGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(2): Show |
2 | a0001c0001t0001 a0001c0001t0005 |
3 | HG02280.hp1 HG02572.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141_-133dupGCCGCC others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(8): Show |
6 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0022 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-147_-133dupGCCGCC others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(11): Show |
2 | a0001c0017t0038 a0006c0025t0041 |
2 | HG03195.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-150_-133dupGCCGCC others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(14): Show |
1 | a0004c0004t0004 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153_-133dupGCCGCC others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(17): Show |
1 | a0003c0003t0013 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-156_-133dupGCCGCC others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(23): Show |
1 | a0001c0001t0001 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162_-133dupGCCGCC others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | C | CCCGCCGC others(41): Show |
2 | a0001c0008t0040 a0010c0014t0047 |
2 | HG02895.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-133_-132insGCCGCC others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | CCCG | C | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(33): Show |
115 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-133delGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | CCCGCCG | C | 3 | a0001c0001t0014 a0001c0001t0042 a0002c0002t0004 |
4 | HG03453.hp1 HG03704.hp2 NA18906.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-138_-133delGCCGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | CCCGCCGC others(2): Show |
C | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(5): Show |
9 | HG00673.hp1 HG03130.hp2 HG03225.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-141_-133delGCCGCC others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | CCCGCCGC others(5): Show |
C | 3 | a0001c0001t0001 a0002c0002t0019 a0004c0004t0004 |
4 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-144_-133delGCCGCC others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578458 | CCCGCCGC others(14): Show |
C | 1 | a0003c0003t0009 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153_-133delGCCGCC others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | |||||
chr18:33578472 | C | A | 1 | a0002c0002t0019 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 160 | chr18 | 33578472 | ||||||
chr18:33578473 | G | C | 1 | a0002c0002t0019 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 159 | chr18 | 33578473 | ||||||
chr18:33578497 | G | A | 2 | a0001c0001t0021 a0001c0005t0020 |
2 | NA18999.hp1 NA18999.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 135 | chr18 | 33578497 | ||||||
chr18:33578500 | A | G | 4 | a0001c0001t0018 a0001c0001t0021 a0001c0005t0020 others(1): Show |
4 | HG02886.hp2 HG03209.hp2 NA18999.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-132A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | chr18 | 33578500 | ||||||
chr18:33578503 | G | A | 1 | a0001c0001t0021 | 1 | NA18999.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 129 | chr18 | 33578503 | ||||||
chr18:33578504 | C | A | 1 | a0001c0005t0020 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 128 | chr18 | 33578504 | ||||||
chr18:33746927 | A | G | 1 | a0002c0002t0046 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 332 | chr18 | 33746927 | ||||||
chr18:33746933 | C | A | 1 | a0001c0001t0011 | 2 | HG01891.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*338C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 338 | chr18 | 33746933 | ||||||
chr18:33747246 | C | G | 1 | a0001c0001t0010 | 3 | HG04184.hp1 NA18989.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*651C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 651 | chr18 | 33747246 | ||||||
chr18:33747332 | A | C | 28 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(25): Show |
67 | HG00558.hp2 HG00621.hp2 HG01255.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*737A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 737 | chr18 | 33747332 | ||||||
chr18:33747347 | G | T | 1 | a0001c0016t0045 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 752 | chr18 | 33747347 | ||||||
chr18:33747413 | GA | G | 4 | a0002c0006t0007 a0003c0003t0044 a0009c0023t0032 others(1): Show |
9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*834delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 834 | INFO_REALIGN_3_PRIME | chr18 | 33747413 | |||||
chr18:33747756 | T | G | 1 | a0003c0003t0044 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1161T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1161 | chr18 | 33747756 | ||||||
chr18:33747885 | G | A | 1 | a0001c0001t0022 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1290 | chr18 | 33747885 | ||||||
chr18:33747921 | C | T | 1 | a0012c0022t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1326 | chr18 | 33747921 | ||||||
chr18:33747944 | C | T | 1 | a0006c0010t0015 | 2 | HG01255.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1349 | chr18 | 33747944 | ||||||
chr18:33748119 | TG | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(42): Show |
159 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*1532delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1532 | INFO_REALIGN_3_PRIME | chr18 | 33748119 | |||||
chr18:33748234 | G | A | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1639 | chr18 | 33748234 | ||||||
chr18:33748316 | T | A | 1 | a0002c0002t0023 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1721 | chr18 | 33748316 | ||||||
chr18:33748378 | G | A | 1 | a0015c0026t0036 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1783 | chr18 | 33748378 | ||||||
chr18:33748555 | C | T | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
92 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1960 | chr18 | 33748555 | ||||||
chr18:33748600 | A | G | 1 | a0001c0001t0014 | 2 | HG03704.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2005 | chr18 | 33748600 | ||||||
chr18:33748679 | C | T | 1 | a0001c0001t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2084 | chr18 | 33748679 | ||||||
chr18:33748756 | T | G | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(42): Show |
159 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2161T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2161 | chr18 | 33748756 | ||||||
chr18:33748856 | C | A | 1 | a0001c0001t0006 | 7 | HG00438.hp1 HG02129.hp2 NA18959.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2261C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2261 | chr18 | 33748856 | ||||||
chr18:33748914 | A | T | 1 | a0002c0013t0027 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2319 | chr18 | 33748914 | ||||||
chr18:33749076 | C | CT | 9 | a0001c0001t0035 a0002c0002t0004 a0002c0002t0019 others(6): Show |
28 | HG00438.hp2 HG00673.hp2 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2498dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2499 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | |||||
chr18:33749076 | CT | C | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(31): Show |
145 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2498delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2498 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | |||||
chr18:33749076 | CTT | C | 5 | a0001c0001t0029 a0001c0017t0038 a0003c0003t0013 others(2): Show |
6 | HG00735.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2497_*2498delTT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2497 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | |||||
chr18:33749439 | AT | A | 7 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0030 others(4): Show |
15 | HG00438.hp1 HG01070.hp2 HG02129.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2857delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2857 | INFO_REALIGN_3_PRIME | chr18 | 33749439 | |||||
chr18:33749551 | C | G | 1 | a0002c0006t0043 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2956C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2956 | chr18 | 33749551 | ||||||
chr18:33749728 | A | G | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3133 | chr18 | 33749728 | ||||||
chr18:33749729 | A | G | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3134A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3134 | chr18 | 33749729 | ||||||
chr18:33749733 | A | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3138A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3138 | chr18 | 33749733 | ||||||
chr18:33749746 | C | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3151C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3151 | chr18 | 33749746 | ||||||
chr18:33749748 | A | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3153A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3153 | chr18 | 33749748 | ||||||
chr18:33749750 | C | A | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3155C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3155 | chr18 | 33749750 | ||||||
chr18:33749756 | A | G | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3161A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3161 | chr18 | 33749756 | ||||||
chr18:33749757 | G | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3162G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3162 | chr18 | 33749757 | ||||||
chr18:33749759 | T | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3164 | chr18 | 33749759 | ||||||
chr18:33749761 | G | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3166G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3166 | chr18 | 33749761 | ||||||
chr18:33749763 | G | GTTCACCA others(5): Show |
1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3168_*3169insTTCA others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3169 | chr18 | 33749763 | ||||||
chr18:33749764 | C | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3169 | chr18 | 33749764 | ||||||
chr18:33749767 | G | A | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3172G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3172 | chr18 | 33749767 | ||||||
chr18:33749768 | G | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3173 | chr18 | 33749768 | ||||||
chr18:33749770 | T | A | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3175T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3175 | chr18 | 33749770 | ||||||
chr18:33749771 | G | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3176G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3176 | chr18 | 33749771 | ||||||
chr18:33749772 | C | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3177C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3177 | chr18 | 33749772 | ||||||
chr18:33749776 | A | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3181A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3181 | chr18 | 33749776 | ||||||
chr18:33749777 | A | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3182 | chr18 | 33749777 | ||||||
chr18:33749778 | A | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3183A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3183 | chr18 | 33749778 | ||||||
chr18:33749779 | G | C | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3184G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3184 | chr18 | 33749779 | ||||||
chr18:33749781 | C | T | 1 | a0004c0004t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3186C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3186 | chr18 | 33749781 | ||||||
chr18:33749991 | C | T | 1 | a0001c0001t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3396C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3396 | chr18 | 33749991 | ||||||
chr18:33750402 | C | G | 3 | a0001c0008t0017 a0001c0008t0040 a0001c0017t0038 |
3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3807C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3807 | chr18 | 33750402 | ||||||
chr18:33750511 | C | T | 1 | a0012c0022t0033 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3916C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3916 | chr18 | 33750511 | ||||||
chr18:33750568 | A | AT | 19 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(16): Show |
56 | HG00558.hp2 HG00621.hp2 HG01884.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3985dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3986 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | |||||
chr18:33750568 | AT | A | 5 | a0001c0001t0011 a0001c0001t0042 a0006c0010t0015 others(2): Show |
7 | HG01255.hp2 HG01891.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3985delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3985 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | |||||
chr18:33750568 | ATT | A | 18 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(15): Show |
93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3984_*3985delTT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3984 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | |||||
chr18:33750845 | C | G | 1 | a0002c0002t0025 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4250C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4250 | chr18 | 33750845 | ||||||
chr18:33751033 | G | GAA | 23 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(20): Show |
60 | HG00558.hp2 HG00621.hp2 HG01884.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4441_*4442dupAA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4443 | INFO_REALIGN_3_PRIME | chr18 | 33751033 | |||||
chr18:33751107 | A | T | 1 | a0001c0001t0042 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4512A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4512 | chr18 | 33751107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33578701 | C | A | 1 | a0001c0005t0002g0002 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.54+16C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578701 | |||||||
chr18:33578779 | C | T | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+94C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578779 | |||||||
chr18:33578868 | G | T | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54+183G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578868 | |||||||
chr18:33578882 | A | T | 2 | a0001c0001t0002g0216 a0002c0002t0003g0217 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.54+197A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578882 | |||||||
chr18:33578904 | G | GCGTCCGG others(3): Show |
2 | a0003c0003t0044g0215 a0004c0004t0004g0214 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54+222_54+231dupTC others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33578904 | ||||||
chr18:33578989 | C | T | 1 | a0001c0001t0011g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+304C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578989 | |||||||
chr18:33578991 | C | T | 22 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(19): Show |
22 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+306C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578991 | |||||||
chr18:33579023 | G | A | 1 | a0016c0019t0034g0003 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54+338G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579023 | |||||||
chr18:33579075 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.54+390A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579075 | |||||||
chr18:33579122 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0003c0003t0009g0011 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+437T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579122 | |||||||
chr18:33579232 | A | G | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+547A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579232 | |||||||
chr18:33579835 | C | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0012g0187 |
3 | HG01070.hp1 HG01071.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.54+1150C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579835 | |||||||
chr18:33580029 | C | A | 26 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(23): Show |
27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+1344C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580029 | |||||||
chr18:33580364 | A | G | 1 | a0006c0010t0015g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.54+1679A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580364 | |||||||
chr18:33580437 | A | G | 19 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0002g0183 others(16): Show |
19 | HG01109.hp2 HG02257.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+1752A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580437 | |||||||
chr18:33580534 | G | T | 1 | a0002c0002t0004g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.54+1849G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580534 | |||||||
chr18:33580608 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0011g0213 a0004c0004t0004g0176 |
3 | HG01891.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.54+1923A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580608 | |||||||
chr18:33581031 | C | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(65): Show |
69 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.54+2346C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581031 | |||||||
chr18:33581136 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.54+2451A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581136 | |||||||
chr18:33581148 | T | A | 26 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(23): Show |
27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+2463T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581148 | |||||||
chr18:33581209 | C | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+2524C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581209 | |||||||
chr18:33581379 | T | G | 19 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(16): Show |
19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+2694T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581379 | |||||||
chr18:33581462 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.54+2777T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581462 | |||||||
chr18:33581472 | A | AGT | 8 | a0001c0001t0001g0147 a0001c0001t0002g0171 a0001c0001t0002g0211 others(5): Show |
8 | HG00735.hp1 HG02129.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+2815_54+2816dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGT | 2 | a0001c0001t0002g0212 a0001c0001t0018g0028 |
2 | HG02886.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.54+2813_54+2816dup others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGT | 16 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0005g0034 others(13): Show |
16 | HG01109.hp2 HG02257.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.54+2811_54+2816dup others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(1): Show |
2 | a0002c0006t0007g0036 a0004c0004t0004g0214 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54+2809_54+2816dup others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0014g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 |
3 | HG03453.hp1 HG03704.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.54+2807_54+2816dup others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0010g0153 a0001c0008t0040g0219 a0001c0017t0038g0174 others(1): Show |
4 | HG02895.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2805_54+2816dup others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(7): Show |
4 | a0001c0001t0001g0156 a0001c0001t0006g0155 a0001c0001t0006g0157 others(1): Show |
4 | HG04204.hp2 NA18959.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+2803_54+2816dup others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(9): Show |
14 | a0001c0001t0001g0160 a0001c0001t0002g0166 a0001c0001t0002g0183 others(11): Show |
14 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.54+2801_54+2816dup others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | A | AGTGTGTG others(11): Show |
4 | a0001c0001t0002g0170 a0002c0002t0004g0167 a0002c0002t0046g0169 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2799_54+2816dup others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581472 | AGT | A | 3 | a0001c0001t0001g0037 a0002c0002t0004g0038 a0011c0012t0001g0039 |
3 | HG00741.hp1 HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.54+2815_54+2816del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | ||||||
chr18:33581652 | C | A | 1 | a0004c0004t0004g0214 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.54+2967C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581652 | |||||||
chr18:33581652 | C | G | 26 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(23): Show |
27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+2967C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581652 | |||||||
chr18:33581688 | G | T | 1 | a0002c0002t0004g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.54+3003G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581688 | |||||||
chr18:33581707 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.54+3022C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581707 | |||||||
chr18:33581955 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54+3270G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581955 | |||||||
chr18:33581989 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+3304T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581989 | |||||||
chr18:33582049 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+3364A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582049 | |||||||
chr18:33582100 | C | G | 22 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(19): Show |
23 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.54+3415C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582100 | |||||||
chr18:33582145 | T | C | 18 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(15): Show |
19 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+3460T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582145 | |||||||
chr18:33582206 | G | T | 1 | a0002c0002t0003g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54+3521G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582206 | |||||||
chr18:33582409 | T | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(58): Show |
62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+3724T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582409 | |||||||
chr18:33582428 | A | G | 19 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(16): Show |
19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+3743A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582428 | |||||||
chr18:33582547 | A | ATTTG | 61 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(58): Show |
62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+3865_54+3866ins others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582547 | ||||||
chr18:33582698 | G | T | 22 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(19): Show |
22 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+4013G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582698 | |||||||
chr18:33582706 | C | CTG | 25 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(22): Show |
25 | HG00280.hp1 HG01361.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.54+4055_54+4056dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | ||||||
chr18:33582706 | C | CTGTG | 8 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0005g0012 others(5): Show |
8 | HG00558.hp1 HG00741.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+4053_54+4056dup others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | ||||||
chr18:33582706 | CTG | C | 51 | a0001c0001t0001g0131 a0001c0001t0001g0138 a0001c0001t0001g0156 others(48): Show |
51 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.54+4055_54+4056del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | ||||||
chr18:33582706 | CTGTG | C | 11 | a0001c0001t0001g0141 a0001c0001t0001g0205 a0001c0001t0001g0206 others(8): Show |
11 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.54+4053_54+4056del others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | ||||||
chr18:33582736 | G | T | 17 | a0001c0001t0001g0156 a0001c0001t0002g0166 a0001c0001t0002g0170 others(14): Show |
17 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+4051G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582736 | |||||||
chr18:33582738 | G | T | 24 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(21): Show |
24 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.54+4053G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582738 | |||||||
chr18:33582740 | G | GTGTT | 14 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0021 others(11): Show |
15 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.54+4056_54+4057ins others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582740 | ||||||
chr18:33582740 | G | GTT | 13 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0005g0024 others(10): Show |
13 | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4058_54+4059dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582740 | ||||||
chr18:33582740 | G | T | 36 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(33): Show |
36 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.54+4055G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582740 | |||||||
chr18:33583130 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+4445A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583130 | |||||||
chr18:33583252 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0014g0179 others(14): Show |
17 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+4567A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583252 | |||||||
chr18:33583267 | A | G | 4 | a0001c0008t0017g0025 a0001c0017t0038g0174 a0002c0006t0007g0026 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4582A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583267 | |||||||
chr18:33583422 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+4737G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583422 | |||||||
chr18:33583452 | A | G | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.54+4767A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583452 | |||||||
chr18:33583547 | G | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+4862G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583547 | |||||||
chr18:33583651 | T | C | 1 | a0002c0002t0004g0161 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.54+4966T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583651 | |||||||
chr18:33583676 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0127 |
2 | HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.54+4991A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583676 | |||||||
chr18:33583693 | G | T | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+5008G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583693 | |||||||
chr18:33583712 | A | G | 2 | a0001c0001t0006g0203 a0001c0005t0002g0204 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.54+5027A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583712 | |||||||
chr18:33583749 | T | G | 1 | a0002c0002t0003g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54+5064T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583749 | |||||||
chr18:33584059 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+5374G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584059 | |||||||
chr18:33584094 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+5409C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584094 | |||||||
chr18:33584163 | C | A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(59): Show |
63 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.54+5478C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584163 | |||||||
chr18:33584475 | G | A | 1 | a0004c0004t0004g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+5790G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584475 | |||||||
chr18:33584668 | A | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(58): Show |
62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+5983A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584668 | |||||||
chr18:33584729 | A | G | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+6044A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584729 | |||||||
chr18:33584880 | A | ATG | 19 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(16): Show |
19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+6207_54+6208dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33584880 | ||||||
chr18:33584880 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0014g0179 others(14): Show |
17 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+6195A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584880 | |||||||
chr18:33585029 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+6344C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585029 | |||||||
chr18:33585130 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54+6445C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585130 | |||||||
chr18:33585346 | A | G | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+6661A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585346 | |||||||
chr18:33585547 | A | G | 4 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+6862A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585547 | |||||||
chr18:33585681 | T | C | 1 | a0001c0018t0001g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.54+6996T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585681 | |||||||
chr18:33585885 | C | T | 4 | a0001c0001t0002g0166 a0001c0001t0002g0170 a0001c0005t0002g0002 others(1): Show |
4 | HG00621.hp2 NA18994.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+7200C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585885 | |||||||
chr18:33585988 | AT | A | 8 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0003c0003t0009g0011 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+7304delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585988 | |||||||
chr18:33585991 | A | C | 8 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0003c0003t0009g0011 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+7306A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585991 | |||||||
chr18:33586181 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+7496A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586181 | |||||||
chr18:33586192 | CTGT | C | 21 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(18): Show |
21 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.54+7512_54+7514del others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586192 | ||||||
chr18:33586404 | C | CTT | 22 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0005g0012 others(19): Show |
23 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.54+7727_54+7728dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586404 | ||||||
chr18:33586404 | C | CTTT | 44 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0166 others(41): Show |
44 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.54+7726_54+7728dup others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586404 | ||||||
chr18:33586545 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54+7860A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586545 | |||||||
chr18:33586621 | G | T | 1 | a0001c0001t0031g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54+7936G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586621 | |||||||
chr18:33586661 | G | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.54+7976G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586661 | |||||||
chr18:33586826 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.54+8141A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586826 | |||||||
chr18:33586892 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0003c0003t0009g0011 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+8207T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586892 | |||||||
chr18:33587226 | C | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(63): Show |
67 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.54+8541C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587226 | |||||||
chr18:33587283 | G | A | 1 | a0001c0001t0009g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.54+8598G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587283 | |||||||
chr18:33587319 | C | T | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+8634C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587319 | |||||||
chr18:33587731 | C | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54+9046C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587731 | |||||||
chr18:33588010 | AGTCT | A | 4 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0008g0033 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+9330_54+9333del others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588010 | ||||||
chr18:33588061 | A | C | 1 | a0002c0002t0023g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.54+9376A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588061 | |||||||
chr18:33588359 | G | GT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0008t0017g0025 others(3): Show |
6 | HG02055.hp1 HG02723.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+9688dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | ||||||
chr18:33588359 | G | GTT | 57 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(54): Show |
58 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.54+9687_54+9688dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | ||||||
chr18:33588359 | G | GTTT | 5 | a0001c0001t0002g0171 a0001c0001t0006g0157 a0001c0008t0040g0219 others(2): Show |
5 | HG02630.hp2 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+9686_54+9688dup others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | ||||||
chr18:33588447 | G | A | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+9762G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588447 | |||||||
chr18:33588449 | T | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.54+9764T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588449 | |||||||
chr18:33588551 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0011g0137 a0002c0002t0004g0120 |
3 | HG02486.hp2 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.54+9866C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588551 | |||||||
chr18:33588750 | A | C | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+10065A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588750 | |||||||
chr18:33588841 | T | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0149 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+10156T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588841 | |||||||
chr18:33588859 | C | T | 1 | a0002c0002t0003g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.54+10174C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588859 | |||||||
chr18:33589018 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(58): Show |
62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+10333T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589018 | |||||||
chr18:33589199 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0030g0064 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.54+10514A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589199 | |||||||
chr18:33589350 | C | A | 1 | a0003c0003t0013g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54+10665C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589350 | |||||||
chr18:33589454 | C | T | 8 | a0001c0001t0014g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+10769C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589454 | |||||||
chr18:33589554 | A | G | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54+10869A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589554 | |||||||
chr18:33589816 | A | G | 4 | a0001c0008t0017g0025 a0001c0017t0038g0174 a0002c0006t0007g0026 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+11131A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589816 | |||||||
chr18:33590105 | T | A | 2 | a0001c0001t0001g0070 a0014c0021t0001g0071 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11420T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590105 | |||||||
chr18:33590107 | C | G | 2 | a0001c0001t0001g0070 a0014c0021t0001g0071 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11422C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590107 | |||||||
chr18:33590108 | TATG | T | 2 | a0001c0001t0001g0070 a0014c0021t0001g0071 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11424_54+11426d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590108 | |||||||
chr18:33590111 | G | GT | 7 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0212 others(4): Show |
7 | HG02647.hp2 HG03688.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+11445dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(9): Show |
1 | a0003c0003t0013g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54+11435_54+11436i others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+11433_54+11445d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(7): Show |
4 | a0001c0001t0002g0183 a0001c0001t0042g0182 a0001c0008t0040g0219 others(1): Show |
4 | HG02895.hp1 NA19043.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+11432_54+11445d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(8): Show |
4 | a0001c0001t0005g0016 a0002c0002t0004g0180 a0002c0006t0007g0030 others(1): Show |
4 | HG02895.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+11431_54+11445d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(9): Show |
12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
12 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+11430_54+11445d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(10): Show |
9 | a0001c0001t0001g0008 a0001c0001t0008g0033 a0001c0001t0014g0179 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+11429_54+11445d others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(11): Show |
11 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0007 others(8): Show |
11 | HG01884.hp1 HG02572.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+11428_54+11445d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(12): Show |
15 | a0001c0001t0005g0024 a0001c0001t0006g0157 a0001c0001t0008g0018 others(12): Show |
15 | HG00621.hp2 HG00735.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+11427_54+11445d others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(13): Show |
2 | a0001c0001t0002g0166 a0001c0020t0001g0154 |
2 | HG04204.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.54+11445_54+11446i others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(14): Show |
1 | a0006c0010t0015g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.54+11445_54+11446i others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0008g0001 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54+11445_54+11446i others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590111 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0008g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.54+11445_54+11446i others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | ||||||
chr18:33590153 | A | G | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.54+11468A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590153 | |||||||
chr18:33590244 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+11559C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590244 | |||||||
chr18:33590426 | G | A | 1 | a0015c0026t0036g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.54+11741G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590426 | |||||||
chr18:33590631 | T | C | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.54+11946T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590631 | |||||||
chr18:33590631 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.54+11946T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590631 | |||||||
chr18:33590753 | A | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54+12068A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590753 | |||||||
chr18:33591116 | A | T | 1 | a0001c0001t0008g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.54+12431A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591116 | |||||||
chr18:33591240 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.54+12555C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591240 | |||||||
chr18:33591278 | G | A | 1 | a0001c0001t0022g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54+12593G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591278 | |||||||
chr18:33591314 | A | G | 1 | a0002c0002t0003g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.54+12629A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591314 | |||||||
chr18:33591396 | T | C | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+12711T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591396 | |||||||
chr18:33591486 | A | C | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.54+12801A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591486 | |||||||
chr18:33591591 | G | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(58): Show |
62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+12906G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591591 | |||||||
chr18:33591638 | CT | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(61): Show |
65 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.54+12968delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33591638 | ||||||
chr18:33591665 | G | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+12980G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591665 | |||||||
chr18:33591703 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.54+13018G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591703 | |||||||
chr18:33591850 | C | T | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.54+13165C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591850 | |||||||
chr18:33591883 | C | T | 5 | a0001c0001t0001g0008 a0003c0003t0009g0011 a0003c0003t0013g0006 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+13198C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591883 | |||||||
chr18:33591924 | A | G | 9 | a0001c0001t0014g0179 a0001c0001t0042g0182 a0002c0002t0004g0180 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+13239A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591924 | |||||||
chr18:33591934 | T | G | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+13249T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591934 | |||||||
chr18:33591942 | T | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+13257T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591942 | |||||||
chr18:33592495 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+13810A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592495 | |||||||
chr18:33592532 | C | T | 1 | a0009c0023t0032g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.54+13847C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592532 | |||||||
chr18:33592533 | G | A | 1 | a0002c0002t0004g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.54+13848G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592533 | |||||||
chr18:33592578 | T | G | 66 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0160 others(63): Show |
67 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.54+13893T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592578 | |||||||
chr18:33592594 | T | C | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54+13909T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592594 | |||||||
chr18:33592637 | G | A | 18 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(15): Show |
19 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+13952G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592637 | |||||||
chr18:33592847 | C | G | 6 | a0001c0001t0002g0171 a0001c0008t0017g0025 a0001c0017t0038g0174 others(3): Show |
6 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+14162C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592847 | |||||||
chr18:33592866 | A | G | 1 | a0005c0024t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54+14181A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592866 | |||||||
chr18:33592937 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.54+14252C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592937 | |||||||
chr18:33593223 | T | C | 78 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0156 others(75): Show |
79 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.55-14371T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593223 | |||||||
chr18:33593258 | C | CT | 60 | a0001c0001t0001g0060 a0001c0001t0001g0126 a0001c0001t0001g0156 others(57): Show |
60 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.55-14313dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | ||||||
chr18:33593258 | C | CTT | 7 | a0001c0008t0017g0025 a0002c0002t0003g0217 a0002c0002t0004g0167 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-14314_55-14313d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | ||||||
chr18:33593258 | CT | C | 5 | a0001c0001t0001g0081 a0001c0001t0005g0016 a0002c0002t0004g0075 others(2): Show |
5 | HG02965.hp1 HG02965.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-14313delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | ||||||
chr18:33593342 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.55-14252C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593342 | |||||||
chr18:33593564 | G | T | 84 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0126 others(81): Show |
85 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-14030G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593564 | |||||||
chr18:33593591 | C | T | 4 | a0001c0001t0014g0179 a0001c0001t0042g0182 a0007c0009t0002g0158 others(1): Show |
4 | HG02886.hp1 HG03225.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-14003C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593591 | |||||||
chr18:33593866 | C | G | 9 | a0001c0001t0001g0008 a0001c0001t0005g0034 a0001c0001t0005g0035 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-13728C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593866 | |||||||
chr18:33594211 | G | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.55-13383G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594211 | |||||||
chr18:33594242 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0005g0034 a0001c0001t0005g0035 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-13352G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594242 | |||||||
chr18:33594369 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.55-13225T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594369 | |||||||
chr18:33594408 | C | G | 30 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(27): Show |
30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.55-13186C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594408 | |||||||
chr18:33594428 | C | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55-13166C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594428 | |||||||
chr18:33594578 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-13016T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594578 | |||||||
chr18:33594698 | A | G | 4 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0042g0182 others(1): Show |
4 | HG01109.hp2 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-12896A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594698 | |||||||
chr18:33594752 | A | G | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55-12842A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594752 | |||||||
chr18:33594801 | C | A | 1 | a0002c0002t0004g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.55-12793C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594801 | |||||||
chr18:33594842 | T | C | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.55-12752T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594842 | |||||||
chr18:33594898 | G | C | 1 | a0002c0006t0007g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.55-12696G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594898 | |||||||
chr18:33595042 | C | G | 1 | a0004c0004t0003g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.55-12552C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595042 | |||||||
chr18:33595184 | C | T | 24 | a0001c0001t0001g0126 a0001c0001t0002g0122 a0001c0001t0002g0123 others(21): Show |
24 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-12410C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595184 | |||||||
chr18:33595221 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55-12373T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595221 | |||||||
chr18:33595518 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.55-12076A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595518 | |||||||
chr18:33595545 | T | C | 1 | a0001c0001t0006g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.55-12049T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595545 | |||||||
chr18:33595688 | A | G | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-11906A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595688 | |||||||
chr18:33596084 | T | C | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-11510T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596084 | |||||||
chr18:33596254 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-11340A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596254 | |||||||
chr18:33596264 | A | G | 46 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(43): Show |
46 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.55-11330A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596264 | |||||||
chr18:33596271 | G | T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-11323G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596271 | |||||||
chr18:33596278 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.55-11316T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596278 | |||||||
chr18:33596486 | A | G | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.55-11108A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596486 | |||||||
chr18:33596538 | G | A | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-11056G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596538 | |||||||
chr18:33596621 | A | G | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-10973A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596621 | |||||||
chr18:33596969 | C | A | 1 | a0001c0001t0010g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.55-10625C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596969 | |||||||
chr18:33597049 | G | A | 137 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(134): Show |
138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.55-10545G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597049 | |||||||
chr18:33597094 | C | T | 2 | a0001c0001t0018g0028 a0002c0002t0004g0146 |
2 | HG00673.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.55-10500C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597094 | |||||||
chr18:33597099 | C | G | 43 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(40): Show |
43 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.55-10495C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597099 | |||||||
chr18:33597278 | A | G | 1 | a0002c0002t0003g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.55-10316A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597278 | |||||||
chr18:33597318 | G | A | 1 | a0001c0001t0005g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-10276G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597318 | |||||||
chr18:33597409 | A | C | 74 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(71): Show |
74 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.55-10185A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597409 | |||||||
chr18:33597535 | A | G | 134 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(131): Show |
135 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.55-10059A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597535 | |||||||
chr18:33597781 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.55-9813T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597781 | |||||||
chr18:33597793 | C | CA | 8 | a0001c0001t0001g0194 a0001c0001t0006g0085 a0001c0001t0006g0191 others(5): Show |
8 | HG00438.hp1 HG00673.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-9788dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33597793 | ||||||
chr18:33597793 | CA | C | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.55-9788delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33597793 | ||||||
chr18:33597802 | A | C | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-9792A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597802 | |||||||
chr18:33597811 | A | C | 1 | a0002c0002t0003g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55-9783A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597811 | |||||||
chr18:33597812 | A | C | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-9782A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597812 | |||||||
chr18:33597815 | AC | A | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.55-9778delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597815 | |||||||
chr18:33597816 | C | A | 1 | a0001c0001t0002g0170 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.55-9778C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597816 | |||||||
chr18:33597913 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.55-9681C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597913 | |||||||
chr18:33597953 | A | G | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.55-9641A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597953 | |||||||
chr18:33598248 | T | C | 1 | a0001c0001t0009g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.55-9346T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598248 | |||||||
chr18:33598475 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.55-9119G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598475 | |||||||
chr18:33598504 | T | C | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-9090T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598504 | |||||||
chr18:33598846 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.55-8748G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598846 | |||||||
chr18:33598912 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55-8682G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598912 | |||||||
chr18:33598971 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55-8623T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598971 | |||||||
chr18:33599039 | A | G | 8 | a0001c0001t0002g0171 a0001c0001t0042g0182 a0001c0008t0017g0025 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-8555A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599039 | |||||||
chr18:33599057 | G | C | 1 | a0004c0004t0003g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.55-8537G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599057 | |||||||
chr18:33599230 | A | T | 1 | a0002c0002t0004g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.55-8364A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599230 | |||||||
chr18:33599231 | T | A | 1 | a0002c0002t0004g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.55-8363T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599231 | |||||||
chr18:33599306 | G | T | 1 | a0001c0001t0010g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.55-8288G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599306 | |||||||
chr18:33599921 | G | A | 1 | a0002c0002t0003g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.55-7673G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599921 | |||||||
chr18:33600476 | C | T | 1 | a0001c0001t0029g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.55-7118C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600476 | |||||||
chr18:33600497 | G | GT | 43 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(40): Show |
43 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.55-7091dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600497 | ||||||
chr18:33600511 | GAAGTTTT others(12): Show |
G | 13 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(10): Show |
13 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-7073_55-7055del others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600511 | ||||||
chr18:33600786 | G | T | 56 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(53): Show |
56 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.55-6808G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600786 | |||||||
chr18:33600821 | C | A | 2 | a0002c0006t0007g0029 a0002c0006t0007g0030 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.55-6773C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600821 | |||||||
chr18:33600845 | C | CA | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-6748dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600845 | ||||||
chr18:33600955 | A | G | 1 | a0002c0002t0025g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.55-6639A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600955 | |||||||
chr18:33601745 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.55-5849G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601745 | |||||||
chr18:33601785 | G | GTATATAT others(17): Show |
1 | a0005c0024t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.55-5799_55-5798ins others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(19): Show |
1 | a0001c0008t0017g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.55-5799_55-5798ins others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(23): Show |
2 | a0001c0001t0008g0033 a0004c0004t0004g0214 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(25): Show |
5 | a0001c0001t0002g0065 a0001c0001t0014g0053 a0002c0002t0003g0042 others(2): Show |
5 | HG00741.hp2 HG01433.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(32): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(27): Show |
10 | a0001c0001t0005g0012 a0001c0001t0005g0016 a0001c0001t0008g0018 others(7): Show |
10 | HG01070.hp2 HG01361.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(34): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(29): Show |
9 | a0001c0001t0001g0126 a0001c0001t0002g0122 a0001c0001t0005g0017 others(6): Show |
10 | HG02559.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(36): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(31): Show |
11 | a0001c0001t0001g0055 a0001c0001t0002g0123 a0001c0001t0005g0013 others(8): Show |
11 | HG00642.hp1 HG00673.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(38): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(33): Show |
11 | a0001c0001t0002g0124 a0001c0001t0005g0015 a0001c0001t0005g0022 others(8): Show |
11 | HG00741.hp1 HG01943.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(40): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(35): Show |
8 | a0001c0001t0002g0171 a0001c0001t0005g0024 a0002c0002t0003g0068 others(5): Show |
8 | HG00323.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTATATAT others(39): Show |
2 | a0001c0001t0002g0216 a0002c0002t0003g0135 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(46): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTGTATAT others(3): Show |
7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(3): Show |
8 | a0001c0001t0014g0179 a0002c0002t0004g0180 a0002c0002t0004g0181 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(15): Show |
3 | a0002c0002t0004g0080 a0002c0002t0004g0177 a0002c0013t0027g0079 |
3 | HG00438.hp2 HG01975.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(17): Show |
1 | a0006c0010t0015g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(19): Show |
1 | a0001c0005t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(23): Show |
1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(25): Show |
2 | a0002c0002t0004g0167 a0007c0009t0002g0158 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(32): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(27): Show |
2 | a0001c0017t0038g0174 a0010c0014t0047g0004 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(34): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(29): Show |
5 | a0001c0001t0002g0140 a0001c0001t0006g0155 a0004c0004t0004g0045 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(36): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(31): Show |
6 | a0001c0001t0001g0156 a0001c0001t0002g0170 a0001c0001t0006g0157 others(3): Show |
6 | HG00280.hp2 NA19003.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(38): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(33): Show |
7 | a0001c0001t0029g0164 a0001c0005t0002g0061 a0001c0005t0002g0165 others(4): Show |
7 | HG00621.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(40): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(35): Show |
7 | a0001c0001t0001g0040 a0001c0001t0002g0166 a0001c0001t0010g0153 others(4): Show |
7 | HG00558.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(37): Show |
2 | a0001c0001t0002g0183 a0001c0008t0040g0219 |
2 | HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(44): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(39): Show |
3 | a0001c0005t0020g0062 a0002c0002t0004g0120 a0016c0019t0034g0003 |
3 | HG02486.hp2 NA18999.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(46): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601785 | G | GTTTATAT others(41): Show |
1 | a0001c0001t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(48): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | ||||||
chr18:33601795 | A | G | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55-5799A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601795 | |||||||
chr18:33601910 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55-5684C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601910 | |||||||
chr18:33601942 | C | T | 1 | a0002c0002t0004g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.55-5652C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601942 | |||||||
chr18:33602059 | T | C | 67 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(64): Show |
67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.55-5535T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33602059 | |||||||
chr18:33602187 | T | C | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-5407T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33602187 | |||||||
chr18:33602803 | GATCAAAT others(26): Show |
G | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-4788_55-4756del others(33): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33602803 | ||||||
chr18:33603396 | G | A | 1 | a0004c0004t0004g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.55-4198G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603396 | |||||||
chr18:33603435 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55-4159C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603435 | |||||||
chr18:33603445 | C | T | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-4149C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603445 | |||||||
chr18:33603571 | A | T | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-4023A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603571 | |||||||
chr18:33603617 | T | A | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-3977T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603617 | |||||||
chr18:33603619 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-3975C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603619 | |||||||
chr18:33603715 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.55-3879G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603715 | |||||||
chr18:33603877 | A | T | 1 | a0001c0001t0002g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.55-3717A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603877 | |||||||
chr18:33603878 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55-3716A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603878 | |||||||
chr18:33604421 | C | T | 5 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-3173C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604421 | |||||||
chr18:33604449 | G | GA | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-3140dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33604449 | ||||||
chr18:33604607 | C | T | 52 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(49): Show |
53 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.55-2987C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604607 | |||||||
chr18:33604617 | A | G | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-2977A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604617 | |||||||
chr18:33604622 | G | A | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.55-2972G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604622 | |||||||
chr18:33604646 | C | CT | 4 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-2946dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33604646 | ||||||
chr18:33604667 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-2927G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604667 | |||||||
chr18:33605092 | C | T | 6 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(3): Show |
6 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-2502C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605092 | |||||||
chr18:33605252 | A | G | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-2342A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605252 | |||||||
chr18:33605411 | T | C | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55-2183T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605411 | |||||||
chr18:33605680 | T | C | 1 | a0002c0002t0003g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.55-1914T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605680 | |||||||
chr18:33605732 | G | A | 52 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(49): Show |
53 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.55-1862G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605732 | |||||||
chr18:33605888 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.55-1706C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605888 | |||||||
chr18:33605920 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55-1674G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605920 | |||||||
chr18:33606130 | C | T | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.55-1464C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606130 | |||||||
chr18:33606153 | A | G | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1441A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606153 | |||||||
chr18:33606374 | G | T | 1 | a0001c0016t0045g0199 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.55-1220G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606374 | |||||||
chr18:33606636 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-958T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606636 | |||||||
chr18:33606772 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55-822C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606772 | |||||||
chr18:33606777 | A | G | 5 | a0001c0001t0001g0194 a0001c0001t0006g0191 a0001c0001t0006g0203 others(2): Show |
5 | HG00673.hp1 NA18982.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-817A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606777 | |||||||
chr18:33607021 | C | G | 137 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(134): Show |
138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.55-573C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33607021 | |||||||
chr18:33607145 | C | G | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.55-449C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33607145 | |||||||
chr18:33607742 | G | A | 66 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(63): Show |
66 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.137+66G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607742 | |||||||
chr18:33607822 | G | A | 1 | a0001c0001t0005g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+146G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607822 | |||||||
chr18:33607946 | C | A | 38 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.137+270C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607946 | |||||||
chr18:33607970 | T | G | 3 | a0001c0001t0002g0007 a0003c0003t0009g0172 a0003c0003t0009g0173 |
3 | HG02258.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.137+294T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607970 | |||||||
chr18:33608121 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137+445G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608121 | |||||||
chr18:33608176 | G | A | 31 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(28): Show |
31 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+500G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608176 | |||||||
chr18:33608929 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.137+1253G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608929 | |||||||
chr18:33608932 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137+1256C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608932 | |||||||
chr18:33608973 | CT | C | 67 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(64): Show |
67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.137+1308delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33608973 | ||||||
chr18:33609211 | A | T | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+1535A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609211 | |||||||
chr18:33609293 | A | G | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+1617A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609293 | |||||||
chr18:33609377 | G | C | 7 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0002c0006t0007g0029 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+1701G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609377 | |||||||
chr18:33609459 | C | T | 1 | a0002c0002t0004g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.137+1783C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609459 | |||||||
chr18:33609514 | T | C | 1 | a0002c0002t0003g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137+1838T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609514 | |||||||
chr18:33609592 | A | G | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+1916A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609592 | |||||||
chr18:33609884 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137+2208T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609884 | |||||||
chr18:33609903 | T | C | 2 | a0001c0017t0038g0174 a0010c0014t0047g0004 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.137+2227T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609903 | |||||||
chr18:33610059 | G | T | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.137+2383G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610059 | |||||||
chr18:33610527 | A | G | 1 | a0002c0002t0023g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.137+2851A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610527 | |||||||
chr18:33610529 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0030g0064 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.137+2853C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610529 | |||||||
chr18:33610545 | A | G | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+2869A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610545 | |||||||
chr18:33610580 | C | T | 3 | a0001c0001t0002g0183 a0001c0008t0040g0219 a0016c0019t0034g0003 |
3 | HG02895.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137+2904C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610580 | |||||||
chr18:33610668 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.137+2992C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610668 | |||||||
chr18:33610691 | T | G | 1 | a0002c0002t0003g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137+3015T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610691 | |||||||
chr18:33610716 | C | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(27): Show |
30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.137+3040C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610716 | |||||||
chr18:33610746 | C | T | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+3070C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610746 | |||||||
chr18:33610801 | GATATTTA | G | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+3129_137+3135d others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33610801 | ||||||
chr18:33611215 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137+3539G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611215 | |||||||
chr18:33611305 | T | C | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.137+3629T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611305 | |||||||
chr18:33611347 | T | C | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+3671T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611347 | |||||||
chr18:33611583 | T | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+3907T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611583 | |||||||
chr18:33611842 | G | A | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+4166G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611842 | |||||||
chr18:33611916 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.137+4240C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611916 | |||||||
chr18:33611959 | T | TA | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+4284dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33611959 | ||||||
chr18:33612106 | G | A | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+4430G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612106 | |||||||
chr18:33612106 | G | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+4430G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612106 | |||||||
chr18:33612184 | C | CAT | 33 | a0001c0001t0001g0076 a0001c0001t0001g0105 a0001c0001t0001g0126 others(30): Show |
33 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.137+4522_137+4523d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | ||||||
chr18:33612184 | C | CATAT | 2 | a0001c0001t0014g0179 a0002c0006t0007g0036 |
2 | HG02145.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.137+4520_137+4523d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | ||||||
chr18:33612184 | C | CATATAT | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+4518_137+4523d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | ||||||
chr18:33612565 | A | G | 54 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(51): Show |
55 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.137+4889A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612565 | |||||||
chr18:33612668 | G | A | 1 | a0002c0002t0004g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.137+4992G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612668 | |||||||
chr18:33612835 | C | A | 1 | a0004c0004t0004g0214 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137+5159C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612835 | |||||||
chr18:33612863 | T | C | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+5187T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612863 | |||||||
chr18:33613335 | C | G | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+5659C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613335 | |||||||
chr18:33613525 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG00558.hp1 HG02148.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+5849T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613525 | |||||||
chr18:33613585 | T | A | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.137+5909T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613585 | |||||||
chr18:33613614 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.137+5938A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613614 | |||||||
chr18:33613678 | G | A | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.137+6002G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613678 | |||||||
chr18:33613800 | A | G | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+6124A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613800 | |||||||
chr18:33614066 | A | G | 1 | a0001c0001t0005g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.137+6390A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614066 | |||||||
chr18:33614163 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0002g0104 a0001c0001t0039g0102 |
3 | NA18971.hp2 NA19003.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.137+6487A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614163 | |||||||
chr18:33614284 | C | T | 1 | a0001c0001t0018g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.137+6608C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614284 | |||||||
chr18:33614435 | C | T | 1 | a0007c0009t0002g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137+6759C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614435 | |||||||
chr18:33614556 | T | C | 1 | a0001c0001t0021g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.137+6880T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614556 | |||||||
chr18:33614588 | A | G | 1 | a0002c0002t0003g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.137+6912A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614588 | |||||||
chr18:33614672 | T | A | 2 | a0002c0002t0003g0142 a0002c0002t0003g0143 |
2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.137+6996T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614672 | |||||||
chr18:33614821 | CT | C | 6 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(3): Show |
6 | HG01943.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+7157delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33614821 | ||||||
chr18:33614980 | G | A | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+7304G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614980 | |||||||
chr18:33615179 | A | G | 1 | a0003c0003t0013g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.137+7503A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615179 | |||||||
chr18:33615238 | T | C | 1 | a0001c0005t0002g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137+7562T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615238 | |||||||
chr18:33615460 | G | A | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+7784G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615460 | |||||||
chr18:33615841 | A | G | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+8165A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615841 | |||||||
chr18:33615845 | C | T | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.137+8169C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615845 | |||||||
chr18:33616039 | A | G | 7 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0002c0006t0007g0029 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+8363A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616039 | |||||||
chr18:33616128 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.137+8452A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616128 | |||||||
chr18:33616177 | T | C | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+8501T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616177 | |||||||
chr18:33616366 | C | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0190 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+8690C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616366 | |||||||
chr18:33616398 | C | CTG | 53 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0001t0001g0126 others(50): Show |
54 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.137+8752_137+8753d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | C | CTGTG | 3 | a0001c0001t0018g0028 a0002c0002t0003g0056 a0002c0002t0003g0142 |
3 | HG02886.hp2 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.137+8750_137+8753d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTG | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0044 others(43): Show |
46 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.137+8752_137+8753d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTGTG | C | 4 | a0001c0001t0002g0090 a0001c0008t0017g0025 a0005c0024t0005g0027 others(1): Show |
4 | HG02723.hp2 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+8750_137+8753d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTGTGTG | C | 34 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(31): Show |
34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+8748_137+8753d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTGTGTGT others(1): Show |
C | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+8746_137+8753d others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.137+8742_137+8753d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616398 | CTGTGTGT others(7): Show |
C | 29 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(26): Show |
29 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.137+8740_137+8753d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | ||||||
chr18:33616665 | T | A | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+8989T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616665 | |||||||
chr18:33616701 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.137+9025A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616701 | |||||||
chr18:33617030 | T | C | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.137+9354T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617030 | |||||||
chr18:33617274 | T | C | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.137+9598T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617274 | |||||||
chr18:33617297 | G | A | 4 | a0001c0001t0006g0191 a0001c0001t0006g0203 a0001c0001t0010g0195 others(1): Show |
4 | NA18982.hp1 NA18998.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+9621G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617297 | |||||||
chr18:33617367 | C | T | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+9691C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617367 | |||||||
chr18:33617368 | G | A | 29 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(26): Show |
29 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.137+9692G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617368 | |||||||
chr18:33617390 | CTGAGGCA others(6): Show |
C | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+9716_137+9728d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33617390 | ||||||
chr18:33617924 | T | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+10248T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617924 | |||||||
chr18:33617954 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.137+10278C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617954 | |||||||
chr18:33618085 | T | C | 1 | a0006c0010t0015g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137+10409T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618085 | |||||||
chr18:33618325 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137+10649A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618325 | |||||||
chr18:33618655 | G | T | 2 | a0001c0001t0002g0171 a0002c0002t0019g0178 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+10979G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618655 | |||||||
chr18:33618769 | TTGA | T | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+11096_137+1109 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33618769 | ||||||
chr18:33618831 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.137+11155A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618831 | |||||||
chr18:33619159 | C | G | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+11483C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619159 | |||||||
chr18:33619446 | GA | G | 41 | a0001c0001t0001g0076 a0001c0001t0001g0188 a0001c0001t0001g0206 others(38): Show |
41 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.137+11785delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | ||||||
chr18:33619446 | GAA | G | 89 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0126 others(86): Show |
90 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.137+11784_137+1178 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | ||||||
chr18:33619446 | GAAA | G | 6 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+11783_137+1178 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | ||||||
chr18:33619455 | A | T | 8 | a0001c0001t0002g0171 a0001c0001t0042g0182 a0001c0008t0017g0025 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+11779A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619455 | |||||||
chr18:33619499 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
9 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+11823C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619499 | |||||||
chr18:33619560 | T | C | 14 | a0001c0001t0001g0156 a0001c0001t0002g0166 a0001c0001t0002g0170 others(11): Show |
14 | HG00558.hp2 HG00621.hp2 HG04184.hp1 others(11): Show |
intron_variant | MODIFIER | c.137+11884T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619560 | |||||||
chr18:33619741 | T | C | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+12065T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619741 | |||||||
chr18:33619809 | C | T | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+12133C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619809 | |||||||
chr18:33619867 | C | G | 32 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(29): Show |
32 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.137+12191C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619867 | |||||||
chr18:33620431 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.137+12755C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620431 | |||||||
chr18:33620491 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+12815G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620491 | |||||||
chr18:33620713 | A | C | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+13037A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620713 | |||||||
chr18:33620836 | C | G | 32 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(29): Show |
32 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.137+13160C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620836 | |||||||
chr18:33620943 | A | G | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+13267A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620943 | |||||||
chr18:33621364 | G | A | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+13688G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621364 | |||||||
chr18:33621378 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137+13702G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621378 | |||||||
chr18:33621443 | C | A | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.137+13767C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621443 | |||||||
chr18:33621462 | A | G | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+13786A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621462 | |||||||
chr18:33621541 | T | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+13865T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621541 | |||||||
chr18:33622142 | G | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+14466G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622142 | |||||||
chr18:33622189 | T | A | 5 | a0001c0001t0002g0140 a0004c0004t0004g0045 a0004c0004t0004g0058 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+14513T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622189 | |||||||
chr18:33622229 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137+14553G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622229 | |||||||
chr18:33622246 | C | T | 1 | a0002c0002t0003g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.137+14570C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622246 | |||||||
chr18:33622308 | GT | G | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+14633delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622308 | |||||||
chr18:33622353 | G | A | 34 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(31): Show |
34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+14677G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622353 | |||||||
chr18:33622397 | T | G | 67 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(64): Show |
67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.137+14721T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622397 | |||||||
chr18:33622413 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+14737T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622413 | |||||||
chr18:33622587 | G | A | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+14911G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622587 | |||||||
chr18:33622803 | A | T | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+15127A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622803 | |||||||
chr18:33623014 | T | A | 1 | a0016c0019t0034g0003 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137+15338T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623014 | |||||||
chr18:33623083 | C | G | 6 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(3): Show |
6 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+15407C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623083 | |||||||
chr18:33623091 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0035g0098 a0002c0002t0004g0075 |
3 | HG00621.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.137+15415A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623091 | |||||||
chr18:33623259 | A | G | 1 | a0009c0023t0032g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.137+15583A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623259 | |||||||
chr18:33623336 | C | T | 35 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+15660C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623336 | |||||||
chr18:33623659 | C | T | 54 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(51): Show |
55 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.137+15983C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623659 | |||||||
chr18:33623795 | T | C | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.137+16119T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623795 | |||||||
chr18:33623830 | A | C | 1 | a0002c0006t0043g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137+16154A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623830 | |||||||
chr18:33623855 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0097 |
2 | HG00323.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.137+16179A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623855 | |||||||
chr18:33623965 | T | C | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+16289T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623965 | |||||||
chr18:33624009 | C | A | 1 | a0001c0001t0006g0191 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.137+16333C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624009 | |||||||
chr18:33624237 | A | G | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+16561A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624237 | |||||||
chr18:33624264 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137+16588G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624264 | |||||||
chr18:33624264 | G | C | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+16588G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624264 | |||||||
chr18:33624766 | T | G | 1 | a0004c0004t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.137+17090T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624766 | |||||||
chr18:33624974 | C | T | 2 | a0001c0001t0002g0200 a0006c0025t0041g0005 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.137+17298C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624974 | |||||||
chr18:33625059 | A | G | 2 | a0001c0001t0002g0171 a0002c0002t0019g0178 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+17383A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625059 | |||||||
chr18:33625152 | A | C | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+17476A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625152 | |||||||
chr18:33625225 | C | G | 30 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(27): Show |
30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.137+17549C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625225 | |||||||
chr18:33625245 | G | A | 24 | a0001c0001t0001g0126 a0001c0001t0002g0122 a0001c0001t0002g0123 others(21): Show |
24 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.137+17569G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625245 | |||||||
chr18:33625324 | A | T | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.137+17648A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625324 | |||||||
chr18:33625730 | G | A | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+18054G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625730 | |||||||
chr18:33625988 | T | G | 16 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(13): Show |
17 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.137+18312T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625988 | |||||||
chr18:33626030 | A | G | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.137+18354A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626030 | |||||||
chr18:33626202 | T | C | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+18526T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626202 | |||||||
chr18:33626360 | T | A | 216 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(213): Show |
217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.138-18534T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626360 | |||||||
chr18:33626385 | A | G | 105 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(102): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.138-18509A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626385 | |||||||
chr18:33626416 | C | A | 136 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.138-18478C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626416 | |||||||
chr18:33626657 | A | T | 137 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(134): Show |
138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.138-18237A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626657 | |||||||
chr18:33628037 | C | A | 1 | a0001c0001t0010g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138-16857C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628037 | |||||||
chr18:33628489 | G | A | 68 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0126 others(65): Show |
68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16405G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628489 | |||||||
chr18:33628532 | A | T | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-16362A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628532 | |||||||
chr18:33628568 | A | T | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-16326A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628568 | |||||||
chr18:33628688 | G | A | 1 | a0002c0002t0003g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.138-16206G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628688 | |||||||
chr18:33628696 | T | A | 68 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0126 others(65): Show |
68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16198T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628696 | |||||||
chr18:33628754 | TC | T | 68 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0126 others(65): Show |
68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16139delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628754 | |||||||
chr18:33628831 | T | G | 1 | a0001c0005t0002g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.138-16063T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628831 | |||||||
chr18:33628982 | G | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.138-15912G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628982 | |||||||
chr18:33629491 | T | C | 1 | a0002c0002t0004g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.138-15403T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33629491 | |||||||
chr18:33629814 | C | T | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.138-15080C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33629814 | |||||||
chr18:33630020 | C | T | 5 | a0001c0001t0002g0065 a0001c0001t0008g0033 a0001c0001t0018g0028 others(2): Show |
5 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-14874C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630020 | |||||||
chr18:33630066 | G | T | 6 | a0001c0001t0002g0171 a0001c0001t0042g0182 a0001c0008t0017g0025 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-14828G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630066 | |||||||
chr18:33630112 | G | C | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-14782G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630112 | |||||||
chr18:33630168 | G | A | 127 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0076 others(124): Show |
128 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.138-14726G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630168 | |||||||
chr18:33630246 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.138-14648C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630246 | |||||||
chr18:33630274 | G | C | 1 | a0006c0010t0015g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138-14620G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630274 | |||||||
chr18:33630386 | C | CT | 39 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0156 others(36): Show |
39 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.138-14498dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33630386 | ||||||
chr18:33630408 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.138-14486A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630408 | |||||||
chr18:33630509 | G | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-14385G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630509 | |||||||
chr18:33630609 | T | G | 1 | a0002c0002t0003g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.138-14285T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630609 | |||||||
chr18:33630645 | C | A | 1 | a0002c0002t0003g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138-14249C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630645 | |||||||
chr18:33631050 | A | C | 1 | a0001c0001t0018g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.138-13844A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631050 | |||||||
chr18:33631122 | ACATT | A | 5 | a0001c0001t0002g0065 a0001c0001t0008g0033 a0001c0001t0018g0028 others(2): Show |
5 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-13771_138-1376 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631122 | |||||||
chr18:33631241 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0031g0066 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.138-13653A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631241 | |||||||
chr18:33631295 | A | C | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.138-13599A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631295 | |||||||
chr18:33631373 | A | G | 18 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.138-13521A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631373 | |||||||
chr18:33631555 | T | C | 1 | a0001c0001t0011g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.138-13339T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631555 | |||||||
chr18:33631656 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-13238T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631656 | |||||||
chr18:33631846 | T | A | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138-13048T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631846 | |||||||
chr18:33631863 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.138-13031A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631863 | |||||||
chr18:33632002 | A | G | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.138-12892A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632002 | |||||||
chr18:33632245 | G | A | 68 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0126 others(65): Show |
68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-12649G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632245 | |||||||
chr18:33632248 | T | A | 7 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0003c0003t0009g0011 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-12646T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632248 | |||||||
chr18:33632644 | A | G | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-12250A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632644 | |||||||
chr18:33632801 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.138-12093C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632801 | |||||||
chr18:33632881 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138-12013T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632881 | |||||||
chr18:33633166 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-11728A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633166 | |||||||
chr18:33633374 | A | G | 1 | a0004c0004t0004g0214 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.138-11520A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633374 | |||||||
chr18:33633562 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.138-11332C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633562 | |||||||
chr18:33633575 | G | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0149 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-11319G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633575 | |||||||
chr18:33633579 | C | T | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-11315C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633579 | |||||||
chr18:33633667 | C | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-11227C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633667 | |||||||
chr18:33633737 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.138-11157C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633737 | |||||||
chr18:33633843 | CA | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(74): Show |
77 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.138-11029delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | ||||||
chr18:33633843 | CAA | C | 25 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0140 others(22): Show |
26 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.138-11030_138-1102 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | ||||||
chr18:33633843 | CAAA | C | 43 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0002g0166 others(40): Show |
43 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.138-11031_138-1102 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | ||||||
chr18:33633875 | CAATT | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG00558.hp1 HG02148.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-11015_138-1101 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633875 | ||||||
chr18:33633893 | G | A | 1 | a0001c0001t0018g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.138-11001G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633893 | |||||||
chr18:33633999 | T | C | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-10895T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633999 | |||||||
chr18:33634161 | G | T | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-10733G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634161 | |||||||
chr18:33634285 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0030g0064 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.138-10609A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634285 | |||||||
chr18:33634667 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-10227A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634667 | |||||||
chr18:33634810 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-10084C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634810 | |||||||
chr18:33634872 | G | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-10022G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634872 | |||||||
chr18:33634929 | T | C | 1 | a0001c0001t0031g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.138-9965T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634929 | |||||||
chr18:33634964 | A | T | 45 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.138-9930A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634964 | |||||||
chr18:33634986 | G | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.138-9908G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634986 | |||||||
chr18:33635031 | A | T | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-9863A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635031 | |||||||
chr18:33635311 | T | C | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138-9583T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635311 | |||||||
chr18:33635354 | T | C | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-9540T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635354 | |||||||
chr18:33635516 | A | C | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.138-9378A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635516 | |||||||
chr18:33635730 | T | A | 4 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-9164T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635730 | |||||||
chr18:33635848 | A | G | 8 | a0001c0001t0002g0171 a0001c0001t0042g0182 a0001c0008t0017g0025 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-9046A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635848 | |||||||
chr18:33636115 | G | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.138-8779G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636115 | |||||||
chr18:33636281 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-8613C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636281 | |||||||
chr18:33636305 | T | TCAA | 6 | a0001c0001t0014g0179 a0001c0008t0017g0025 a0002c0002t0003g0063 others(3): Show |
6 | HG01981.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-8562_138-8560d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | ||||||
chr18:33636305 | T | TCAACAA | 2 | a0001c0001t0042g0182 a0003c0003t0044g0215 |
2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138-8565_138-8560d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | ||||||
chr18:33636305 | TCAACAAC others(5): Show |
T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.138-8571_138-8560d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | ||||||
chr18:33636329 | ACAACAG | A | 34 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(31): Show |
34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.138-8559_138-8554d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636329 | ||||||
chr18:33636331 | AACAGCAA others(11): Show |
A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0092 a0001c0001t0002g0007 others(8): Show |
11 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-8559_138-8542d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636331 | ||||||
chr18:33636332 | ACAG | A | 3 | a0002c0002t0004g0167 a0004c0004t0004g0045 a0006c0010t0015g0168 |
3 | HG01255.hp2 HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.138-8559_138-8557d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636332 | ||||||
chr18:33636334 | AGCAACAA others(8): Show |
A | 69 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(66): Show |
70 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.138-8559_138-8545d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636334 | |||||||
chr18:33636335 | G | A | 21 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0081 others(18): Show |
21 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-8559G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636335 | |||||||
chr18:33636337 | A | C | 7 | a0001c0001t0002g0171 a0001c0001t0042g0182 a0001c0008t0017g0025 others(4): Show |
7 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-8557A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636337 | |||||||
chr18:33636337 | AACAACAA others(5): Show |
A | 19 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0081 others(16): Show |
19 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.138-8529_138-8518d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636337 | ||||||
chr18:33636340 | AACAACAG others(2): Show |
A | 2 | a0001c0001t0001g0093 a0006c0025t0041g0005 |
2 | HG02602.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.138-8547_138-8539d others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636340 | ||||||
chr18:33636349 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-8545C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636349 | |||||||
chr18:33636412 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-8482G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636412 | |||||||
chr18:33636568 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.138-8326G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636568 | |||||||
chr18:33636626 | A | G | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-8268A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636626 | |||||||
chr18:33636792 | T | C | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-8102T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636792 | |||||||
chr18:33636805 | T | A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0008g0033 others(6): Show |
9 | HG00673.hp2 HG02258.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-8089T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636805 | |||||||
chr18:33636806 | A | T | 2 | a0002c0002t0001g0113 a0002c0002t0019g0178 |
2 | HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.138-8088A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636806 | |||||||
chr18:33637104 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-7790C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637104 | |||||||
chr18:33637230 | A | G | 152 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.138-7664A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637230 | |||||||
chr18:33637251 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.138-7643A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637251 | |||||||
chr18:33637422 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.138-7472A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637422 | |||||||
chr18:33637460 | A | G | 2 | a0002c0002t0003g0135 a0002c0002t0024g0133 |
2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.138-7434A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637460 | |||||||
chr18:33637625 | T | G | 2 | a0001c0001t0014g0053 a0002c0002t0003g0042 |
2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.138-7269T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637625 | |||||||
chr18:33637981 | G | A | 6 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-6913G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637981 | |||||||
chr18:33638005 | A | C | 87 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.138-6889A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638005 | |||||||
chr18:33638011 | C | T | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138-6883C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638011 | |||||||
chr18:33638056 | T | C | 4 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6838T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638056 | |||||||
chr18:33638112 | G | A | 44 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(41): Show |
44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.138-6782G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638112 | |||||||
chr18:33638133 | G | GTA | 57 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(54): Show |
58 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.138-6748_138-6747d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33638133 | ||||||
chr18:33638146 | T | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-6748T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638146 | |||||||
chr18:33638159 | TAGTG | T | 4 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0004c0004t0004g0214 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-6734_138-6731d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638159 | |||||||
chr18:33638181 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-6713T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638181 | |||||||
chr18:33638205 | G | GAT | 4 | a0001c0001t0006g0082 a0001c0001t0006g0085 a0002c0002t0004g0130 others(1): Show |
4 | HG00438.hp1 HG02129.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6678_138-6677d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33638205 | ||||||
chr18:33638310 | G | A | 5 | a0001c0001t0001g0194 a0001c0001t0006g0191 a0001c0001t0006g0203 others(2): Show |
5 | HG00673.hp1 NA18982.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-6584G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638310 | |||||||
chr18:33638397 | G | A | 1 | a0001c0001t0005g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.138-6497G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638397 | |||||||
chr18:33638815 | A | T | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.138-6079A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638815 | |||||||
chr18:33638937 | C | T | 5 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(2): Show |
5 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-5957C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638937 | |||||||
chr18:33639130 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.138-5764G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639130 | |||||||
chr18:33639270 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.138-5624C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639270 | |||||||
chr18:33639271 | A | G | 149 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.138-5623A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639271 | |||||||
chr18:33639380 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-5514G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639380 | |||||||
chr18:33639555 | A | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-5339A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639555 | |||||||
chr18:33639815 | T | A | 45 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.138-5079T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639815 | |||||||
chr18:33639838 | T | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5056T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639838 | |||||||
chr18:33639908 | A | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.138-4986A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639908 | |||||||
chr18:33640285 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0008g0033 others(3): Show |
6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-4609C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640285 | |||||||
chr18:33640286 | A | G | 4 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-4608A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640286 | |||||||
chr18:33640333 | C | T | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138-4561C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640333 | |||||||
chr18:33640542 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.138-4352T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640542 | |||||||
chr18:33640789 | A | G | 1 | a0002c0002t0004g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.138-4105A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640789 | |||||||
chr18:33640852 | T | TCA | 147 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.138-4042_138-4041i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640852 | |||||||
chr18:33641331 | C | T | 2 | a0001c0001t0002g0183 a0016c0019t0034g0003 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3563C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641331 | |||||||
chr18:33641332 | G | A | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-3562G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641332 | |||||||
chr18:33641406 | AAAC | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3485_138-3483d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33641406 | ||||||
chr18:33641726 | G | T | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-3168G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641726 | |||||||
chr18:33641871 | T | C | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138-3023T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641871 | |||||||
chr18:33641995 | C | G | 2 | a0001c0001t0001g0156 a0002c0002t0004g0161 |
2 | NA19003.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.138-2899C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641995 | |||||||
chr18:33642118 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-2776A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642118 | |||||||
chr18:33642551 | A | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-2343A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642551 | |||||||
chr18:33642682 | A | T | 1 | a0001c0001t0006g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.138-2212A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642682 | |||||||
chr18:33642880 | G | A | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.138-2014G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642880 | |||||||
chr18:33642953 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.138-1941G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642953 | |||||||
chr18:33643100 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-1794C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643100 | |||||||
chr18:33643159 | C | A | 1 | a0001c0001t0006g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.138-1735C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643159 | |||||||
chr18:33643576 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-1318A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643576 | |||||||
chr18:33643632 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-1262G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643632 | |||||||
chr18:33643745 | T | A | 2 | a0002c0002t0003g0135 a0002c0002t0024g0133 |
2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.138-1149T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643745 | |||||||
chr18:33643760 | T | C | 147 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(144): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.138-1134T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643760 | |||||||
chr18:33643812 | A | G | 82 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(79): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-1082A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643812 | |||||||
chr18:33644203 | A | G | 2 | a0001c0001t0002g0216 a0002c0002t0003g0217 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.138-691A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644203 | |||||||
chr18:33644311 | A | G | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-583A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644311 | |||||||
chr18:33644366 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.138-528G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644366 | |||||||
chr18:33644478 | G | GT | 8 | a0001c0001t0001g0070 a0001c0001t0001g0083 a0001c0001t0002g0122 others(5): Show |
8 | HG01358.hp1 HG02145.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-403dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33644478 | ||||||
chr18:33644482 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-412T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644482 | |||||||
chr18:33644558 | G | T | 3 | a0002c0002t0003g0108 a0002c0002t0003g0109 a0005c0007t0001g0107 |
3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-336G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644558 | |||||||
chr18:33644559 | T | A | 3 | a0002c0002t0003g0108 a0002c0002t0003g0109 a0005c0007t0001g0107 |
3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-335T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644559 | |||||||
chr18:33644560 | A | C | 3 | a0002c0002t0003g0108 a0002c0002t0003g0109 a0005c0007t0001g0107 |
3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-334A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644560 | |||||||
chr18:33644705 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.138-189G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644705 | |||||||
chr18:33644796 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138-98T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644796 | |||||||
chr18:33645066 | G | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(80): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.246+64G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645066 | |||||||
chr18:33645182 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246+180A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645182 | |||||||
chr18:33645402 | T | G | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+400T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645402 | |||||||
chr18:33645499 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0031g0066 a0015c0026t0036g0043 |
3 | HG02055.hp1 HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.246+497G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645499 | |||||||
chr18:33645754 | G | GT | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.247-482dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 33645754 | ||||||
chr18:33646036 | A | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.247-209A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646036 | |||||||
chr18:33646050 | A | T | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.247-195A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646050 | |||||||
chr18:33646094 | T | C | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.247-151T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646094 | |||||||
chr18:33646175 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.247-70C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646175 | |||||||
chr18:33646473 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.355+120C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646473 | |||||||
chr18:33646474 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355+121G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646474 | |||||||
chr18:33646610 | C | T | 194 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.355+257C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646610 | |||||||
chr18:33646635 | G | A | 2 | a0001c0001t0001g0037 a0002c0002t0003g0136 |
2 | HG01943.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.355+282G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646635 | |||||||
chr18:33646880 | C | CG | 59 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0049 others(56): Show |
59 | HG00280.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.355+539dupG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | ||||||
chr18:33646880 | C | CGG | 26 | a0001c0001t0001g0037 a0001c0001t0001g0094 a0001c0001t0001g0100 others(23): Show |
26 | HG00642.hp1 HG00673.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.355+538_355+539dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | ||||||
chr18:33646880 | CG | C | 19 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0131 others(16): Show |
19 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.355+539delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | ||||||
chr18:33646881 | G | C | 8 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+528G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646881 | |||||||
chr18:33646891 | G | A | 8 | a0001c0001t0001g0055 a0001c0001t0014g0053 a0002c0002t0003g0042 others(5): Show |
8 | HG00323.hp1 HG00741.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+538G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646891 | |||||||
chr18:33646892 | G | GA | 15 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0002g0170 others(12): Show |
15 | HG00558.hp2 HG00735.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.355+539_355+540ins others(1): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646892 | |||||||
chr18:33646946 | A | C | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.355+593A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646946 | |||||||
chr18:33646950 | A | G | 1 | a0002c0002t0004g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.355+597A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646950 | |||||||
chr18:33647098 | GTC | G | 5 | a0004c0004t0004g0045 a0004c0004t0004g0058 a0004c0004t0004g0059 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+749_355+750del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33647098 | ||||||
chr18:33647247 | G | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(78): Show |
81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+894G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647247 | |||||||
chr18:33647261 | C | A | 1 | a0001c0001t0002g0196 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.355+908C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647261 | |||||||
chr18:33647287 | C | G | 1 | a0002c0002t0004g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.355+934C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647287 | |||||||
chr18:33647309 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.355+956C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647309 | |||||||
chr18:33647310 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.355+957G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647310 | |||||||
chr18:33647655 | C | T | 4 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1302C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647655 | |||||||
chr18:33647698 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355+1345T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647698 | |||||||
chr18:33647731 | C | A | 1 | a0001c0001t0022g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.355+1378C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647731 | |||||||
chr18:33647797 | T | C | 1 | a0001c0005t0020g0062 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.355+1444T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647797 | |||||||
chr18:33647803 | T | C | 141 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(138): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.355+1450T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647803 | |||||||
chr18:33647850 | A | G | 1 | a0001c0001t0011g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355+1497A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647850 | |||||||
chr18:33647892 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.355+1539G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647892 | |||||||
chr18:33648205 | G | A | 2 | a0001c0001t0002g0183 a0016c0019t0034g0003 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355+1852G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648205 | |||||||
chr18:33648326 | A | T | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.355+1973A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648326 | |||||||
chr18:33648392 | G | A | 1 | a0006c0010t0015g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.355+2039G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648392 | |||||||
chr18:33648692 | TAGAAA | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+2346_355+2350d others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33648692 | ||||||
chr18:33648753 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.355+2400A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648753 | |||||||
chr18:33649683 | G | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.355+3330G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649683 | |||||||
chr18:33649691 | A | T | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+3338A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649691 | |||||||
chr18:33649854 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.355+3501A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649854 | |||||||
chr18:33649888 | C | A | 44 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(41): Show |
44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.355+3535C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649888 | |||||||
chr18:33650020 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.355+3667G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650020 | |||||||
chr18:33650077 | A | C | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.355+3724A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650077 | |||||||
chr18:33650170 | A | C | 4 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0004c0004t0004g0214 others(1): Show |
4 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3817A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650170 | |||||||
chr18:33650265 | G | A | 45 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+3912G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650265 | |||||||
chr18:33650412 | G | C | 1 | a0002c0002t0025g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.355+4059G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650412 | |||||||
chr18:33650442 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.355+4089C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650442 | |||||||
chr18:33650511 | T | C | 6 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0008g0033 others(3): Show |
6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+4158T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650511 | |||||||
chr18:33650540 | A | C | 2 | a0001c0001t0002g0183 a0016c0019t0034g0003 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355+4187A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650540 | |||||||
chr18:33650667 | T | C | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.355+4314T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650667 | |||||||
chr18:33650698 | C | T | 2 | a0001c0001t0002g0171 a0002c0002t0019g0178 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.355+4345C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650698 | |||||||
chr18:33651052 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.355+4699C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33651052 | |||||||
chr18:33651916 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355+5563A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33651916 | |||||||
chr18:33652094 | C | T | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.355+5741C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652094 | |||||||
chr18:33652516 | G | C | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.355+6163G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652516 | |||||||
chr18:33652585 | T | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.355+6232T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652585 | |||||||
chr18:33652603 | C | CAAAAAAA others(3): Show |
75 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0044 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.355+6254_355+6263d others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(4): Show |
21 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0072 others(18): Show |
22 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.355+6253_355+6263d others(13): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0005g0024 a0002c0013t0027g0079 a0003c0003t0009g0011 others(1): Show |
4 | HG00438.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+6252_355+6263d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(9): Show |
26 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0002g0170 others(23): Show |
26 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.355+6263_355+6264i others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0040 a0001c0001t0002g0140 a0001c0001t0002g0166 others(5): Show |
8 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+6263_355+6264i others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(11): Show |
1 | a0001c0005t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.355+6263_355+6264i others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652603 | C | CAAAAAAA others(13): Show |
1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355+6263_355+6264i others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | ||||||
chr18:33652997 | G | A | 2 | a0002c0002t0003g0054 a0002c0002t0003g0056 |
2 | HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.355+6644G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652997 | |||||||
chr18:33653251 | G | A | 25 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
25 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.355+6898G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653251 | |||||||
chr18:33653427 | T | C | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+7074T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653427 | |||||||
chr18:33653441 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.355+7088C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653441 | |||||||
chr18:33653607 | C | T | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.355+7254C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653607 | |||||||
chr18:33653615 | C | A | 1 | a0014c0021t0001g0071 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.355+7262C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653615 | |||||||
chr18:33653708 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.355+7355A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653708 | |||||||
chr18:33653863 | C | CT | 45 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+7520dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33653863 | ||||||
chr18:33654044 | A | G | 1 | a0001c0001t0022g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.356-7572A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654044 | |||||||
chr18:33654373 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.356-7243A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654373 | |||||||
chr18:33654488 | G | T | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-7128G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654488 | |||||||
chr18:33654530 | T | C | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.356-7086T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654530 | |||||||
chr18:33654535 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.356-7081A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654535 | |||||||
chr18:33654596 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.356-7020T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654596 | |||||||
chr18:33654656 | C | G | 5 | a0004c0004t0004g0045 a0004c0004t0004g0058 a0004c0004t0004g0059 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-6960C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654656 | |||||||
chr18:33654656 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-6960C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654656 | |||||||
chr18:33654703 | GC | G | 83 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(80): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.356-6911delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33654703 | ||||||
chr18:33655081 | G | A | 1 | a0004c0004t0003g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.356-6535G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655081 | |||||||
chr18:33655295 | A | G | 1 | a0001c0001t0022g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.356-6321A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655295 | |||||||
chr18:33655314 | A | G | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.356-6302A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655314 | |||||||
chr18:33655334 | A | G | 1 | a0001c0001t0005g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.356-6282A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655334 | |||||||
chr18:33655390 | G | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.356-6226G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655390 | |||||||
chr18:33655572 | T | C | 45 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(42): Show |
45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.356-6044T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655572 | |||||||
chr18:33655631 | A | G | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-5985A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655631 | |||||||
chr18:33655963 | A | T | 1 | a0001c0001t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.356-5653A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655963 | |||||||
chr18:33656116 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0014g0179 |
2 | HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.356-5500G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656116 | |||||||
chr18:33656183 | C | T | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(98): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.356-5433C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656183 | |||||||
chr18:33656281 | G | C | 1 | a0002c0002t0004g0130 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.356-5335G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656281 | |||||||
chr18:33656481 | C | T | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-5135C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656481 | |||||||
chr18:33656643 | A | G | 1 | a0002c0002t0004g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.356-4973A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656643 | |||||||
chr18:33657016 | G | C | 102 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(99): Show |
103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.356-4600G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657016 | |||||||
chr18:33657394 | C | T | 13 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(10): Show |
13 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.356-4222C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657394 | |||||||
chr18:33657502 | A | G | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.356-4114A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657502 | |||||||
chr18:33657710 | G | C | 1 | a0002c0006t0007g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.356-3906G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657710 | |||||||
chr18:33657729 | A | AAC | 3 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0127 |
3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3887_356-3886i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657729 | |||||||
chr18:33657730 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0127 |
3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3886G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657730 | |||||||
chr18:33657731 | A | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0127 |
3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3885A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657731 | |||||||
chr18:33657732 | G | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0127 |
3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3884G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657732 | |||||||
chr18:33657955 | A | G | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.356-3661A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657955 | |||||||
chr18:33658054 | G | A | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.356-3562G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33658054 | |||||||
chr18:33659219 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.356-2397A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659219 | |||||||
chr18:33659380 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.356-2236C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659380 | |||||||
chr18:33659411 | A | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.356-2205A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659411 | |||||||
chr18:33659730 | A | G | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-1886A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659730 | |||||||
chr18:33659786 | T | G | 2 | a0007c0009t0002g0158 a0007c0009t0002g0159 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.356-1830T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659786 | |||||||
chr18:33660189 | A | G | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.356-1427A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660189 | |||||||
chr18:33660299 | C | A | 1 | a0001c0001t0011g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.356-1317C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660299 | |||||||
chr18:33660419 | C | T | 1 | a0001c0001t0009g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-1197C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660419 | |||||||
chr18:33660899 | C | T | 1 | a0002c0006t0043g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356-717C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660899 | |||||||
chr18:33660994 | T | C | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-622T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660994 | |||||||
chr18:33661131 | T | G | 3 | a0001c0001t0001g0099 a0001c0001t0035g0098 a0002c0002t0004g0075 |
3 | HG00621.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.356-485T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661131 | |||||||
chr18:33661241 | T | G | 4 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-375T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661241 | |||||||
chr18:33661246 | T | G | 1 | a0001c0001t0029g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.356-370T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661246 | |||||||
chr18:33661366 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.356-250C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661366 | |||||||
chr18:33661389 | A | G | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.356-227A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661389 | |||||||
chr18:33661435 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356-181C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661435 | |||||||
chr18:33661460 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356-156C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661460 | |||||||
chr18:33661533 | C | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.356-83C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661533 | |||||||
chr18:33661804 | G | C | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+67G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661804 | |||||||
chr18:33661868 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.477+131A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661868 | |||||||
chr18:33661888 | A | G | 6 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0008g0033 others(3): Show |
6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+151A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661888 | |||||||
chr18:33661897 | T | TA | 15 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(12): Show |
16 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.477+169dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33661897 | ||||||
chr18:33661897 | T | TAA | 81 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(78): Show |
81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.477+168_477+169dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33661897 | ||||||
chr18:33661934 | A | G | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.477+197A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661934 | |||||||
chr18:33661991 | C | T | 18 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.477+254C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661991 | |||||||
chr18:33662245 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.477+508G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662245 | |||||||
chr18:33662429 | T | C | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.477+692T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662429 | |||||||
chr18:33662635 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.477+898C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662635 | |||||||
chr18:33662661 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477+924C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662661 | |||||||
chr18:33662947 | T | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(80): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.477+1210T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662947 | |||||||
chr18:33662959 | T | C | 2 | a0001c0001t0042g0182 a0003c0003t0044g0215 |
2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.477+1222T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662959 | |||||||
chr18:33663560 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477+1823A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663560 | |||||||
chr18:33663562 | CTTTGT | C | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+1829_477+1833d others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33663562 | ||||||
chr18:33663693 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.477+1956A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663693 | |||||||
chr18:33663716 | T | C | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+1979T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663716 | |||||||
chr18:33663934 | C | CAT | 47 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(44): Show |
47 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.477+2208_477+2209d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33663934 | ||||||
chr18:33663964 | C | G | 83 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(80): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.477+2227C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663964 | |||||||
chr18:33664247 | G | A | 1 | a0002c0002t0003g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.477+2510G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664247 | |||||||
chr18:33664318 | A | G | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.477+2581A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664318 | |||||||
chr18:33664468 | A | G | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.477+2731A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664468 | |||||||
chr18:33664470 | A | C | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.477+2733A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664470 | |||||||
chr18:33664573 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.477+2836T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664573 | |||||||
chr18:33664689 | G | A | 1 | a0004c0004t0004g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.477+2952G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664689 | |||||||
chr18:33664823 | G | A | 1 | a0003c0003t0009g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.477+3086G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664823 | |||||||
chr18:33664889 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.477+3152C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664889 | |||||||
chr18:33664893 | A | G | 1 | a0002c0002t0004g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.477+3156A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664893 | |||||||
chr18:33664982 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0127 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.477+3245G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664982 | |||||||
chr18:33665200 | A | G | 1 | a0002c0002t0025g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.477+3463A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665200 | |||||||
chr18:33665374 | T | A | 2 | a0002c0006t0007g0029 a0002c0006t0007g0030 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.477+3637T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665374 | |||||||
chr18:33665501 | C | T | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.477+3764C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665501 | |||||||
chr18:33665655 | G | A | 4 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+3918G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665655 | |||||||
chr18:33665739 | T | G | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+4002T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665739 | |||||||
chr18:33665839 | T | C | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+4102T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665839 | |||||||
chr18:33665907 | A | G | 187 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.477+4170A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665907 | |||||||
chr18:33665954 | G | C | 1 | a0002c0002t0003g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.477+4217G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665954 | |||||||
chr18:33666022 | A | G | 4 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+4285A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666022 | |||||||
chr18:33666040 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.477+4303A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666040 | |||||||
chr18:33666055 | G | A | 1 | a0001c0020t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.477+4318G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666055 | |||||||
chr18:33666083 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0008g0033 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.477+4346A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666083 | |||||||
chr18:33666280 | A | G | 1 | a0002c0002t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.478-4393A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666280 | |||||||
chr18:33666331 | C | G | 2 | a0001c0001t0002g0216 a0002c0002t0003g0217 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.478-4342C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666331 | |||||||
chr18:33666630 | G | A | 149 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.478-4043G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666630 | |||||||
chr18:33666956 | A | G | 9 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0002c0006t0007g0029 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.478-3717A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666956 | |||||||
chr18:33667035 | T | C | 1 | a0001c0001t0012g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-3638T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667035 | |||||||
chr18:33667097 | C | T | 29 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(26): Show |
29 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-3576C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667097 | |||||||
chr18:33667323 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.478-3350C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667323 | |||||||
chr18:33667565 | G | A | 1 | a0003c0003t0037g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.478-3108G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667565 | |||||||
chr18:33667618 | C | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3055C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667618 | |||||||
chr18:33667717 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.478-2956C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667717 | |||||||
chr18:33667942 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.478-2731A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667942 | |||||||
chr18:33668124 | C | T | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.478-2549C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668124 | |||||||
chr18:33668359 | T | C | 182 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(179): Show |
183 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.478-2314T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668359 | |||||||
chr18:33668427 | C | CAA | 8 | a0001c0001t0002g0171 a0001c0008t0017g0025 a0002c0002t0019g0178 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2231_478-2230d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | ||||||
chr18:33668427 | CA | C | 87 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.478-2230delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | ||||||
chr18:33668427 | CAA | C | 13 | a0001c0001t0001g0175 a0001c0001t0005g0012 a0001c0001t0005g0013 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-2231_478-2230d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | ||||||
chr18:33668458 | T | A | 18 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.478-2215T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668458 | |||||||
chr18:33668664 | A | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.478-2009A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668664 | |||||||
chr18:33668770 | C | T | 5 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0004c0004t0004g0214 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1903C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668770 | |||||||
chr18:33668895 | A | AAC | 96 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(93): Show |
96 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.478-1765_478-1764d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668895 | ||||||
chr18:33668907 | C | CAT | 5 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1765_478-1764i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668907 | ||||||
chr18:33668961 | G | A | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.478-1712G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668961 | |||||||
chr18:33669033 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0051 |
2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.478-1640G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669033 | |||||||
chr18:33669040 | A | G | 2 | a0006c0010t0015g0168 a0006c0010t0015g0184 |
2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.478-1633A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669040 | |||||||
chr18:33669095 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0002g0051 |
2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.478-1578A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669095 | |||||||
chr18:33669180 | G | T | 1 | a0001c0001t0010g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.478-1493G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669180 | |||||||
chr18:33669447 | C | G | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478-1226C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669447 | |||||||
chr18:33669564 | A | G | 4 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1109A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669564 | |||||||
chr18:33669617 | C | CA | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.478-1055dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33669617 | ||||||
chr18:33669922 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.478-751T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669922 | |||||||
chr18:33669949 | C | A | 1 | a0002c0002t0004g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.478-724C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669949 | |||||||
chr18:33669960 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.478-713T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669960 | |||||||
chr18:33669981 | C | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-692C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669981 | |||||||
chr18:33669984 | C | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-689C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669984 | |||||||
chr18:33670011 | C | A | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.478-662C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33670011 | |||||||
chr18:33670964 | C | T | 24 | a0001c0001t0002g0171 a0001c0001t0005g0012 a0001c0001t0005g0013 others(21): Show |
25 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.595+174C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33670964 | |||||||
chr18:33671053 | C | T | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.595+263C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671053 | |||||||
chr18:33671124 | G | A | 81 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(78): Show |
81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.595+334G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671124 | |||||||
chr18:33671138 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0005g0034 a0001c0001t0005g0035 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+348A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671138 | |||||||
chr18:33671257 | G | T | 191 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(188): Show |
192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.595+467G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671257 | |||||||
chr18:33671312 | G | A | 97 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(94): Show |
97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.596-435G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671312 | |||||||
chr18:33671456 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.596-291C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671456 | |||||||
chr18:33671519 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.596-228C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671519 | |||||||
chr18:33671663 | C | T | 1 | a0009c0023t0032g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.596-84C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671663 | |||||||
chr18:33671674 | C | T | 2 | a0001c0001t0028g0189 a0001c0008t0040g0219 |
2 | HG02486.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.596-73C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671674 | |||||||
chr18:33672165 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(125): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.715+299G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672165 | |||||||
chr18:33672392 | G | A | 1 | a0001c0001t0014g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.715+526G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672392 | |||||||
chr18:33672505 | A | G | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.715+639A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672505 | |||||||
chr18:33672637 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.715+771G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672637 | |||||||
chr18:33672641 | C | T | 133 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(130): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.715+775C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672641 | |||||||
chr18:33672682 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+816G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672682 | |||||||
chr18:33672848 | C | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+982C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672848 | |||||||
chr18:33673108 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(124): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.715+1242A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673108 | |||||||
chr18:33673373 | AT | A | 68 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0156 others(65): Show |
69 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.715+1525delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33673373 | ||||||
chr18:33673373 | ATT | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(77): Show |
80 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.715+1524_715+1525d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33673373 | ||||||
chr18:33673405 | G | T | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.715+1539G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673405 | |||||||
chr18:33673441 | C | T | 30 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(27): Show |
30 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.715+1575C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673441 | |||||||
chr18:33673498 | T | G | 4 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(1): Show |
4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+1632T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673498 | |||||||
chr18:33673621 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+1755C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673621 | |||||||
chr18:33673674 | G | A | 32 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0141 others(29): Show |
32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.715+1808G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673674 | |||||||
chr18:33673831 | G | A | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.715+1965G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673831 | |||||||
chr18:33674049 | G | A | 137 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(134): Show |
137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.715+2183G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674049 | |||||||
chr18:33674399 | T | C | 1 | a0001c0001t0005g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+2533T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674399 | |||||||
chr18:33674399 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.715+2533T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674399 | |||||||
chr18:33674601 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715+2735T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674601 | |||||||
chr18:33674687 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0190 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+2821C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674687 | |||||||
chr18:33674722 | C | G | 1 | a0001c0001t0006g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.715+2856C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674722 | |||||||
chr18:33674747 | T | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(79): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.715+2881T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674747 | |||||||
chr18:33674869 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715+3003C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674869 | |||||||
chr18:33674898 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+3032G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674898 | |||||||
chr18:33674908 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+3042G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674908 | |||||||
chr18:33675082 | C | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(130): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.715+3216C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675082 | |||||||
chr18:33675406 | G | GTT | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+3545_715+3546d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33675406 | ||||||
chr18:33675569 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.715+3703C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675569 | |||||||
chr18:33675692 | T | G | 133 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(130): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.715+3826T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675692 | |||||||
chr18:33675865 | T | C | 13 | a0001c0001t0001g0076 a0001c0001t0005g0012 a0001c0001t0005g0013 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.715+3999T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675865 | |||||||
chr18:33675865 | T | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(29): Show |
32 | HG00673.hp2 HG01071.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.715+3999T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675865 | |||||||
chr18:33675907 | T | C | 32 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(29): Show |
32 | HG00673.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.715+4041T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675907 | |||||||
chr18:33675928 | A | G | 1 | a0001c0018t0001g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.715+4062A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675928 | |||||||
chr18:33675954 | A | G | 85 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0044 others(82): Show |
85 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.715+4088A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675954 | |||||||
chr18:33675999 | C | T | 1 | a0005c0007t0002g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.715+4133C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675999 | |||||||
chr18:33676020 | C | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0018t0001g0069 |
3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.715+4154C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676020 | |||||||
chr18:33676065 | C | A | 4 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0008t0040g0219 others(1): Show |
4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+4199C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676065 | |||||||
chr18:33676148 | C | T | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+4282C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676148 | |||||||
chr18:33676209 | C | T | 2 | a0001c0001t0006g0155 a0001c0001t0006g0157 |
2 | NA18959.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+4343C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676209 | |||||||
chr18:33676222 | C | CA | 16 | a0001c0001t0002g0123 a0001c0001t0002g0171 a0001c0001t0005g0012 others(13): Show |
16 | HG00280.hp2 HG01109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.715+4381dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(3): Show |
1 | a0002c0006t0007g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715+4372_715+4381d others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(6): Show |
3 | a0003c0003t0009g0172 a0004c0004t0004g0214 a0015c0026t0036g0043 |
3 | HG02258.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.715+4369_715+4381d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(7): Show |
1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.715+4368_715+4381d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0042g0182 a0003c0003t0009g0173 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.715+4367_715+4381d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0081 a0001c0001t0001g0117 a0001c0001t0010g0084 others(1): Show |
4 | HG01975.hp1 NA18959.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+4366_715+4381d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0105 a0001c0001t0001g0175 a0001c0001t0001g0186 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.715+4365_715+4381d others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(11): Show |
40 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(37): Show |
40 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.715+4364_715+4381d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(12): Show |
15 | a0001c0001t0001g0050 a0001c0001t0001g0083 a0001c0001t0001g0087 others(12): Show |
15 | HG00438.hp1 HG00642.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.715+4363_715+4381d others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.715+4362_715+4381d others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(14): Show |
2 | a0002c0002t0025g0052 a0013c0015t0001g0115 |
2 | HG00280.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.715+4361_715+4381d others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0006g0191 others(1): Show |
4 | HG00323.hp2 HG01928.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+4360_715+4381d others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.715+4359_715+4381d others(25): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.715+4358_715+4381d others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676222 | CA | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0156 a0001c0001t0001g0206 others(17): Show |
20 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.715+4381delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | ||||||
chr18:33676300 | T | C | 1 | a0004c0004t0004g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.715+4434T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676300 | |||||||
chr18:33676403 | C | G | 82 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(79): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.715+4537C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676403 | |||||||
chr18:33676430 | C | T | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+4564C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676430 | |||||||
chr18:33676431 | T | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+4565T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676431 | |||||||
chr18:33676738 | G | A | 132 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(129): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.715+4872G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676738 | |||||||
chr18:33676989 | G | C | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.715+5123G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676989 | |||||||
chr18:33677261 | A | G | 5 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0004c0004t0004g0214 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+5395A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677261 | |||||||
chr18:33677635 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.715+5769G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677635 | |||||||
chr18:33677769 | C | A | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-5636C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677769 | |||||||
chr18:33677851 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.716-5554T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677851 | |||||||
chr18:33677894 | T | G | 1 | a0001c0001t0002g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.716-5511T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677894 | |||||||
chr18:33678009 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.716-5396C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678009 | |||||||
chr18:33678077 | A | ATTAT | 2 | a0001c0001t0001g0087 a0001c0020t0001g0154 |
2 | HG02148.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.716-5297_716-5294d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | ||||||
chr18:33678077 | ATTAT | A | 87 | a0001c0001t0001g0040 a0001c0001t0001g0097 a0001c0001t0001g0141 others(84): Show |
88 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.716-5297_716-5294d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | ||||||
chr18:33678077 | ATTATTTA others(1): Show |
A | 6 | a0001c0001t0001g0076 a0003c0003t0009g0011 a0003c0003t0013g0006 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-5301_716-5294d others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | ||||||
chr18:33678077 | ATTATTTA others(9): Show |
A | 13 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(10): Show |
13 | HG00673.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.716-5309_716-5294d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | ||||||
chr18:33678235 | T | A | 132 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(129): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.716-5170T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678235 | |||||||
chr18:33678351 | A | C | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.716-5054A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678351 | |||||||
chr18:33678653 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.716-4752C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678653 | |||||||
chr18:33678807 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.716-4598G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678807 | |||||||
chr18:33679058 | CAT | C | 31 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(28): Show |
31 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.716-4346_716-4345d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679058 | |||||||
chr18:33679191 | A | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(124): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.716-4214A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679191 | |||||||
chr18:33679209 | C | A | 78 | a0001c0001t0001g0040 a0001c0001t0001g0070 a0001c0001t0001g0076 others(75): Show |
78 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.716-4196C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679209 | |||||||
chr18:33679211 | A | C | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.716-4194A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679211 | |||||||
chr18:33679582 | A | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-3823A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679582 | |||||||
chr18:33679584 | A | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-3821A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679584 | |||||||
chr18:33679615 | A | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(83): Show |
86 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.716-3790A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679615 | |||||||
chr18:33679670 | G | T | 1 | a0002c0002t0003g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.716-3735G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679670 | |||||||
chr18:33679673 | C | T | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.716-3732C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679673 | |||||||
chr18:33679717 | C | G | 1 | a0002c0002t0004g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.716-3688C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679717 | |||||||
chr18:33679773 | A | G | 1 | a0001c0001t0029g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.716-3632A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679773 | |||||||
chr18:33679787 | A | C | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.716-3618A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679787 | |||||||
chr18:33679832 | C | T | 1 | a0002c0002t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.716-3573C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679832 | |||||||
chr18:33680370 | G | A | 1 | a0001c0001t0005g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.716-3035G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680370 | |||||||
chr18:33680523 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(79): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.716-2882T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680523 | |||||||
chr18:33680530 | A | G | 87 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.716-2875A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680530 | |||||||
chr18:33680544 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.716-2861G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680544 | |||||||
chr18:33681386 | A | G | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.716-2019A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681386 | |||||||
chr18:33681503 | G | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0018t0001g0069 |
3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.716-1902G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681503 | |||||||
chr18:33681549 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.716-1856C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681549 | |||||||
chr18:33681553 | G | C | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-1852G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681553 | |||||||
chr18:33681665 | G | T | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.716-1740G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681665 | |||||||
chr18:33681775 | TA | T | 5 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0004c0004t0004g0214 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.716-1626delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33681775 | ||||||
chr18:33681776 | A | T | 131 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(128): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.716-1629A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681776 | |||||||
chr18:33681827 | A | G | 1 | a0001c0001t0005g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.716-1578A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681827 | |||||||
chr18:33681942 | T | A | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-1463T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681942 | |||||||
chr18:33682032 | T | A | 5 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-1373T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682032 | |||||||
chr18:33682042 | A | T | 1 | a0001c0001t0035g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.716-1363A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682042 | |||||||
chr18:33682113 | G | A | 1 | a0001c0001t0021g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.716-1292G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682113 | |||||||
chr18:33682175 | G | A | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.716-1230G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682175 | |||||||
chr18:33682588 | A | G | 179 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(176): Show |
180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.716-817A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682588 | |||||||
chr18:33682621 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-784C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682621 | |||||||
chr18:33682626 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-779C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682626 | |||||||
chr18:33682702 | A | ACACTGGT others(6): Show |
1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-700_716-699ins others(13): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33682702 | ||||||
chr18:33682711 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-694T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682711 | |||||||
chr18:33682713 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-692A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682713 | |||||||
chr18:33682714 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-691T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682714 | |||||||
chr18:33682717 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-688A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682717 | |||||||
chr18:33682718 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-687A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682718 | |||||||
chr18:33682719 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-686A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682719 | |||||||
chr18:33682720 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-685A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682720 | |||||||
chr18:33682722 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-683A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682722 | |||||||
chr18:33682724 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-681T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682724 | |||||||
chr18:33682726 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-679T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682726 | |||||||
chr18:33682728 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-677T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682728 | |||||||
chr18:33682729 | G | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-676G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682729 | |||||||
chr18:33682730 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-675T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682730 | |||||||
chr18:33682734 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-671T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682734 | |||||||
chr18:33682736 | C | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-669C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682736 | |||||||
chr18:33682737 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-668A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682737 | |||||||
chr18:33682740 | T | TACTTAAG others(3): Show |
1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-665_716-664ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682740 | |||||||
chr18:33682751 | C | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-654C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682751 | |||||||
chr18:33682752 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-653A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682752 | |||||||
chr18:33682755 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-650T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682755 | |||||||
chr18:33682763 | A | T | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-642A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682763 | |||||||
chr18:33682764 | C | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-641C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682764 | |||||||
chr18:33682764 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.716-641C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682764 | |||||||
chr18:33682766 | G | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-639G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682766 | |||||||
chr18:33682770 | T | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-635T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682770 | |||||||
chr18:33682773 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-632A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682773 | |||||||
chr18:33682775 | C | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-630C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682775 | |||||||
chr18:33682776 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-629T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682776 | |||||||
chr18:33682784 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-621T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682784 | |||||||
chr18:33682786 | A | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-619A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682786 | |||||||
chr18:33682788 | G | T | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-617G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682788 | |||||||
chr18:33682790 | A | T | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-615A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682790 | |||||||
chr18:33682792 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-613T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682792 | |||||||
chr18:33682793 | C | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-612C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682793 | |||||||
chr18:33682795 | T | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-610T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682795 | |||||||
chr18:33682798 | T | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-607T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682798 | |||||||
chr18:33682807 | C | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-598C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682807 | |||||||
chr18:33682808 | T | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-597T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682808 | |||||||
chr18:33682813 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-592A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682813 | |||||||
chr18:33682817 | GATGGGAT others(3): Show |
G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-586_716-577del others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33682817 | ||||||
chr18:33682830 | G | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-575G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682830 | |||||||
chr18:33682844 | G | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-561G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682844 | |||||||
chr18:33682845 | C | T | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-560C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682845 | |||||||
chr18:33682847 | G | C | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-558G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682847 | |||||||
chr18:33682852 | T | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-553T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682852 | |||||||
chr18:33682870 | A | G | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.716-535A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682870 | |||||||
chr18:33682872 | G | A | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-533G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682872 | |||||||
chr18:33682885 | T | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-520T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682885 | |||||||
chr18:33683043 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.716-362G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683043 | |||||||
chr18:33683059 | T | C | 83 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(80): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.716-346T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683059 | |||||||
chr18:33683356 | G | A | 178 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.716-49G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683356 | |||||||
chr18:33683639 | A | G | 38 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(35): Show |
38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.879+71A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683639 | |||||||
chr18:33683837 | A | G | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.879+269A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683837 | |||||||
chr18:33683919 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.879+351G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683919 | |||||||
chr18:33683953 | A | G | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+385A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683953 | |||||||
chr18:33683982 | T | C | 2 | a0006c0010t0015g0168 a0006c0010t0015g0184 |
2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+414T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683982 | |||||||
chr18:33684028 | C | G | 44 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(41): Show |
45 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(42): Show |
intron_variant | MODIFIER | c.879+460C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684028 | |||||||
chr18:33684152 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+584A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684152 | |||||||
chr18:33684748 | C | A | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.879+1180C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684748 | |||||||
chr18:33684790 | C | T | 2 | a0001c0005t0002g0061 a0001c0005t0020g0062 |
2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.879+1222C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684790 | |||||||
chr18:33684831 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.879+1263A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684831 | |||||||
chr18:33684936 | G | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1368G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684936 | |||||||
chr18:33685123 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+1555C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685123 | |||||||
chr18:33685447 | G | T | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.879+1879G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685447 | |||||||
chr18:33685464 | G | A | 1 | a0001c0001t0010g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.879+1896G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685464 | |||||||
chr18:33685465 | A | T | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.879+1897A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685465 | |||||||
chr18:33685505 | G | T | 30 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(27): Show |
30 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.879+1937G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685505 | |||||||
chr18:33685633 | G | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+2065G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685633 | |||||||
chr18:33685881 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.879+2313C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685881 | |||||||
chr18:33685915 | C | T | 1 | a0001c0001t0022g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.879+2347C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685915 | |||||||
chr18:33685916 | G | A | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+2348G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685916 | |||||||
chr18:33685955 | G | A | 1 | a0001c0001t0011g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.879+2387G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685955 | |||||||
chr18:33685985 | G | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+2417G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685985 | |||||||
chr18:33686176 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0005g0022 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.879+2608T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686176 | |||||||
chr18:33686331 | C | G | 31 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(28): Show |
31 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+2763C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686331 | |||||||
chr18:33686383 | A | G | 1 | a0002c0002t0003g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.879+2815A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686383 | |||||||
chr18:33686422 | T | C | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+2854T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686422 | |||||||
chr18:33686445 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.879+2877A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686445 | |||||||
chr18:33686484 | A | C | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.879+2916A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686484 | |||||||
chr18:33686506 | G | A | 1 | a0001c0001t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+2938G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686506 | |||||||
chr18:33686613 | T | G | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.879+3045T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686613 | |||||||
chr18:33686777 | A | G | 135 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+3209A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686777 | |||||||
chr18:33687129 | G | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+3561G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687129 | |||||||
chr18:33687373 | A | G | 135 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+3805A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687373 | |||||||
chr18:33687387 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.879+3819G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687387 | |||||||
chr18:33687447 | A | G | 160 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.879+3879A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687447 | |||||||
chr18:33687485 | T | C | 135 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+3917T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687485 | |||||||
chr18:33687747 | T | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.879+4179T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687747 | |||||||
chr18:33687852 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+4284A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687852 | |||||||
chr18:33688101 | C | G | 1 | a0001c0001t0021g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.879+4533C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688101 | |||||||
chr18:33688260 | G | A | 36 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.879+4692G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688260 | |||||||
chr18:33688349 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.879+4781C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688349 | |||||||
chr18:33688671 | G | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+5103G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688671 | |||||||
chr18:33688746 | A | T | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+5178A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688746 | |||||||
chr18:33688915 | A | G | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.879+5347A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688915 | |||||||
chr18:33688971 | A | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(29): Show |
32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+5403A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688971 | |||||||
chr18:33689003 | C | CT | 134 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(131): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.879+5445dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33689003 | ||||||
chr18:33689123 | A | G | 1 | a0003c0003t0009g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+5555A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689123 | |||||||
chr18:33689194 | A | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0100 others(1): Show |
4 | HG01261.hp1 HG01358.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+5626A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689194 | |||||||
chr18:33689253 | C | T | 44 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(41): Show |
45 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(42): Show |
intron_variant | MODIFIER | c.879+5685C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689253 | |||||||
chr18:33689315 | C | T | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+5747C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689315 | |||||||
chr18:33689333 | C | T | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+5765C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689333 | |||||||
chr18:33689339 | T | C | 183 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(180): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.879+5771T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689339 | |||||||
chr18:33689640 | A | G | 135 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+6072A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689640 | |||||||
chr18:33689728 | G | A | 19 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(16): Show |
19 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.879+6160G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689728 | |||||||
chr18:33689975 | A | G | 1 | a0002c0006t0007g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+6407A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689975 | |||||||
chr18:33690384 | C | T | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+6816C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690384 | |||||||
chr18:33690388 | T | C | 4 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0009c0023t0032g0116 others(1): Show |
4 | HG02818.hp1 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+6820T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690388 | |||||||
chr18:33690454 | C | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+6886C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690454 | |||||||
chr18:33690491 | A | G | 1 | a0001c0020t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.879+6923A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690491 | |||||||
chr18:33690589 | C | A | 41 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.879+7021C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690589 | |||||||
chr18:33690615 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.879+7047A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690615 | |||||||
chr18:33690632 | C | T | 1 | a0003c0003t0037g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.879+7064C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690632 | |||||||
chr18:33690715 | A | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0141 a0001c0001t0001g0206 others(29): Show |
32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+7147A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690715 | |||||||
chr18:33690777 | T | C | 185 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(182): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.879+7209T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690777 | |||||||
chr18:33690848 | T | C | 37 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0160 others(34): Show |
37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+7280T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690848 | |||||||
chr18:33690855 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(137): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.879+7287C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690855 | |||||||
chr18:33690937 | C | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+7369C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690937 | |||||||
chr18:33690954 | G | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+7386G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690954 | |||||||
chr18:33691041 | C | T | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.879+7473C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691041 | |||||||
chr18:33691249 | C | G | 2 | a0004c0004t0004g0214 a0015c0026t0036g0043 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.879+7681C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691249 | |||||||
chr18:33691490 | A | C | 3 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0017t0038g0174 |
3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+7922A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691490 | |||||||
chr18:33691509 | A | G | 5 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+7941A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691509 | |||||||
chr18:33691655 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+8087A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691655 | |||||||
chr18:33691703 | A | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+8135A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691703 | |||||||
chr18:33691711 | A | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+8143A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691711 | |||||||
chr18:33691819 | A | G | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.879+8251A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691819 | |||||||
chr18:33691906 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+8338A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691906 | |||||||
chr18:33692051 | C | T | 1 | a0002c0002t0004g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+8483C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692051 | |||||||
chr18:33692174 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.879+8606G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692174 | |||||||
chr18:33692274 | C | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(93): Show |
96 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.879+8706C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692274 | |||||||
chr18:33692438 | A | C | 2 | a0002c0002t0003g0063 a0002c0002t0004g0046 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.879+8870A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692438 | |||||||
chr18:33692439 | T | G | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.879+8871T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692439 | |||||||
chr18:33692500 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+8932C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692500 | |||||||
chr18:33692711 | A | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+9143A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692711 | |||||||
chr18:33693249 | G | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+9681G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693249 | |||||||
chr18:33693300 | A | T | 1 | a0001c0001t0010g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.879+9732A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693300 | |||||||
chr18:33693418 | G | A | 121 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.879+9850G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693418 | |||||||
chr18:33693507 | G | A | 188 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(185): Show |
189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.879+9939G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693507 | |||||||
chr18:33693536 | A | T | 121 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.879+9968A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693536 | |||||||
chr18:33693596 | G | A | 5 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+10028G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693596 | |||||||
chr18:33693683 | T | G | 1 | a0001c0001t0009g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.879+10115T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693683 | |||||||
chr18:33693891 | G | A | 13 | a0001c0001t0001g0055 a0001c0001t0005g0012 a0001c0001t0005g0013 others(10): Show |
14 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+10323G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693891 | |||||||
chr18:33693943 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0160 |
2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.879+10375A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693943 | |||||||
chr18:33694042 | G | T | 6 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG02129.hp1 NA18948.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+10474G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694042 | |||||||
chr18:33694341 | G | A | 187 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(184): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.879+10773G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694341 | |||||||
chr18:33694400 | A | G | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+10832A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694400 | |||||||
chr18:33695030 | C | T | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+11462C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695030 | |||||||
chr18:33695037 | A | G | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+11469A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695037 | |||||||
chr18:33695053 | C | T | 1 | a0002c0006t0007g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.879+11485C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695053 | |||||||
chr18:33695541 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0044 others(96): Show |
99 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.879+11973T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695541 | |||||||
chr18:33695654 | A | T | 1 | a0001c0005t0002g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.879+12086A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695654 | |||||||
chr18:33696109 | G | A | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+12541G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696109 | |||||||
chr18:33696214 | TA | T | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+12653delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33696214 | ||||||
chr18:33696283 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+12715G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696283 | |||||||
chr18:33696287 | T | C | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+12719T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696287 | |||||||
chr18:33696556 | G | T | 2 | a0006c0010t0015g0168 a0006c0010t0015g0184 |
2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+12988G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696556 | |||||||
chr18:33696605 | A | G | 136 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.879+13037A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696605 | |||||||
chr18:33696611 | C | A | 111 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.879+13043C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696611 | |||||||
chr18:33696719 | T | TA | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+13152dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33696719 | ||||||
chr18:33696844 | A | G | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+13276A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696844 | |||||||
chr18:33696862 | G | T | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+13294G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696862 | |||||||
chr18:33696920 | A | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(111): Show |
115 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.879+13352A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696920 | |||||||
chr18:33696981 | T | C | 136 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.879+13413T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696981 | |||||||
chr18:33697003 | T | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+13435T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697003 | |||||||
chr18:33697040 | T | C | 112 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(109): Show |
113 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.879+13472T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697040 | |||||||
chr18:33697165 | C | T | 15 | a0001c0001t0014g0053 a0002c0002t0003g0106 a0002c0002t0003g0108 others(12): Show |
15 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+13597C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697165 | |||||||
chr18:33697215 | A | G | 5 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+13647A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697215 | |||||||
chr18:33697530 | C | T | 1 | a0001c0001t0009g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.879+13962C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697530 | |||||||
chr18:33697627 | A | G | 27 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(24): Show |
27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+14059A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697627 | |||||||
chr18:33697688 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.879+14120A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697688 | |||||||
chr18:33697752 | C | T | 137 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(134): Show |
138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+14184C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697752 | |||||||
chr18:33697754 | A | G | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+14186A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697754 | |||||||
chr18:33697829 | C | G | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+14261C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697829 | |||||||
chr18:33697839 | C | CA | 137 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(134): Show |
138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+14278dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33697839 | ||||||
chr18:33698273 | C | T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+14705C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698273 | |||||||
chr18:33698447 | G | C | 2 | a0006c0010t0015g0168 a0006c0010t0015g0184 |
2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+14879G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698447 | |||||||
chr18:33698576 | T | C | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+15008T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698576 | |||||||
chr18:33698650 | G | C | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.879+15082G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698650 | |||||||
chr18:33698751 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0140 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.879+15183A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698751 | |||||||
chr18:33698859 | C | T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+15291C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698859 | |||||||
chr18:33698960 | A | G | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+15392A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698960 | |||||||
chr18:33699070 | G | A | 1 | a0001c0001t0008g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879+15502G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699070 | |||||||
chr18:33699082 | A | G | 1 | a0002c0002t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879+15514A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699082 | |||||||
chr18:33699470 | T | C | 137 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(134): Show |
138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+15902T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699470 | |||||||
chr18:33699510 | T | C | 1 | a0001c0001t0006g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.879+15942T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699510 | |||||||
chr18:33699541 | G | A | 1 | a0001c0001t0005g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+15973G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699541 | |||||||
chr18:33699548 | T | G | 123 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(120): Show |
124 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.879+15980T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699548 | |||||||
chr18:33699691 | G | A | 20 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+16123G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699691 | |||||||
chr18:33699707 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.879+16139C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699707 | |||||||
chr18:33699907 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG00558.hp1 HG01496.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+16339C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699907 | |||||||
chr18:33699921 | G | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+16353G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699921 | |||||||
chr18:33699939 | T | G | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+16371T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699939 | |||||||
chr18:33700158 | A | G | 138 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(135): Show |
139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.879+16590A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700158 | |||||||
chr18:33700241 | A | ATAGGAAT others(1): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | HG02602.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.879+16674_879+1668 others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33700241 | ||||||
chr18:33700265 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+16697C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700265 | |||||||
chr18:33700286 | G | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+16718G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700286 | |||||||
chr18:33700291 | G | A | 1 | a0007c0009t0002g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+16723G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700291 | |||||||
chr18:33700450 | CA | C | 26 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(23): Show |
26 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.879+16883delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700450 | |||||||
chr18:33700544 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+16976G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700544 | |||||||
chr18:33700616 | G | C | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+17048G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700616 | |||||||
chr18:33701059 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.879+17491T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701059 | |||||||
chr18:33701168 | A | T | 3 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0017t0038g0174 |
3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+17600A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701168 | |||||||
chr18:33701193 | A | C | 27 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(24): Show |
27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+17625A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701193 | |||||||
chr18:33701275 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.879+17707G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701275 | |||||||
chr18:33701607 | T | G | 6 | a0001c0001t0002g0171 a0001c0001t0002g0183 a0001c0001t0028g0189 others(3): Show |
6 | HG02486.hp1 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+18039T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701607 | |||||||
chr18:33701756 | T | C | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+18188T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701756 | |||||||
chr18:33701792 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0010g0195 |
2 | HG00621.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.879+18224A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701792 | |||||||
chr18:33701916 | T | G | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+18348T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701916 | |||||||
chr18:33702127 | A | G | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+18559A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702127 | |||||||
chr18:33702205 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.879+18637G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702205 | |||||||
chr18:33702217 | A | C | 2 | a0001c0001t0002g0183 a0001c0001t0028g0189 |
2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+18649A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702217 | |||||||
chr18:33702356 | C | A | 15 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(12): Show |
15 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+18788C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702356 | |||||||
chr18:33702366 | T | C | 1 | a0001c0016t0045g0199 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.879+18798T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702366 | |||||||
chr18:33702418 | G | C | 138 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(135): Show |
139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.879+18850G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702418 | |||||||
chr18:33702423 | T | C | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+18855T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702423 | |||||||
chr18:33702499 | A | G | 3 | a0001c0001t0008g0018 a0001c0001t0008g0020 a0001c0001t0008g0023 |
3 | HG01884.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.879+18931A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702499 | |||||||
chr18:33702904 | A | G | 1 | a0001c0001t0035g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.879+19336A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702904 | |||||||
chr18:33702969 | G | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+19401G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702969 | |||||||
chr18:33703011 | G | C | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+19443G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703011 | |||||||
chr18:33703239 | T | G | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+19671T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703239 | |||||||
chr18:33703323 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.879+19755G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703323 | |||||||
chr18:33703360 | G | A | 20 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+19792G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703360 | |||||||
chr18:33703440 | G | C | 1 | a0001c0001t0002g0170 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.879+19872G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703440 | |||||||
chr18:33703464 | G | A | 136 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.879+19896G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703464 | |||||||
chr18:33703478 | C | A | 1 | a0001c0005t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.879+19910C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703478 | |||||||
chr18:33703494 | G | A | 2 | a0004c0004t0004g0214 a0015c0026t0036g0043 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.879+19926G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703494 | |||||||
chr18:33703564 | G | A | 1 | a0008c0011t0003g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.879+19996G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703564 | |||||||
chr18:33703835 | T | C | 1 | a0002c0002t0003g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.879+20267T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703835 | |||||||
chr18:33703911 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+20343C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703911 | |||||||
chr18:33704044 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+20476A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704044 | |||||||
chr18:33704134 | G | A | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+20566G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704134 | |||||||
chr18:33704287 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+20719T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704287 | |||||||
chr18:33704367 | G | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+20799G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704367 | |||||||
chr18:33704403 | G | T | 136 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.879+20835G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704403 | |||||||
chr18:33704488 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(198): Show |
202 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.879+20920C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704488 | |||||||
chr18:33704604 | A | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+21036A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704604 | |||||||
chr18:33704642 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+21074A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704642 | |||||||
chr18:33704650 | C | G | 2 | a0001c0001t0006g0112 a0013c0015t0001g0115 |
2 | NA18943.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.879+21082C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704650 | |||||||
chr18:33704801 | C | T | 3 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0017t0038g0174 |
3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+21233C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704801 | |||||||
chr18:33704916 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.879+21348G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704916 | |||||||
chr18:33704943 | T | C | 1 | a0002c0006t0007g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.879+21375T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704943 | |||||||
chr18:33705053 | A | G | 1 | a0004c0004t0003g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.879+21485A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705053 | |||||||
chr18:33705093 | G | A | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+21525G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705093 | |||||||
chr18:33705200 | A | AT | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+21633dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33705200 | ||||||
chr18:33705305 | A | C | 164 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(161): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.879+21737A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705305 | |||||||
chr18:33705339 | C | T | 1 | a0001c0001t0011g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.879+21771C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705339 | |||||||
chr18:33705364 | G | T | 2 | a0001c0001t0002g0211 a0001c0001t0006g0203 |
2 | HG02129.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.879+21796G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705364 | |||||||
chr18:33705573 | C | A | 1 | a0002c0002t0003g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.879+22005C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705573 | |||||||
chr18:33705581 | A | G | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+22013A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705581 | |||||||
chr18:33705607 | T | C | 1 | a0001c0008t0040g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+22039T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705607 | |||||||
chr18:33705611 | C | A | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+22043C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705611 | |||||||
chr18:33705773 | T | A | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22205T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705773 | |||||||
chr18:33705774 | A | T | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22206A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705774 | |||||||
chr18:33705900 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.879+22332G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705900 | |||||||
chr18:33705946 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22378T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705946 | |||||||
chr18:33705947 | C | A | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22379C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705947 | |||||||
chr18:33705948 | A | C | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22380A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705948 | |||||||
chr18:33706001 | A | G | 1 | a0003c0003t0009g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+22433A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706001 | |||||||
chr18:33706107 | CT | C | 169 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(166): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.879+22551delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706107 | ||||||
chr18:33706107 | CTT | C | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.879+22550_879+2255 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706107 | ||||||
chr18:33706165 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+22597C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706165 | |||||||
chr18:33706207 | A | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+22639A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706207 | |||||||
chr18:33706238 | A | G | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+22670A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706238 | |||||||
chr18:33706348 | A | AT | 3 | a0001c0001t0002g0183 a0001c0001t0028g0189 a0001c0017t0038g0174 |
3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+22786dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706348 | ||||||
chr18:33706365 | A | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+22797A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706365 | |||||||
chr18:33706407 | A | C | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22839A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706407 | |||||||
chr18:33706516 | G | A | 136 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.879+22948G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706516 | |||||||
chr18:33706592 | A | G | 54 | a0001c0001t0001g0040 a0001c0001t0001g0070 a0001c0001t0001g0160 others(51): Show |
54 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.879+23024A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706592 | |||||||
chr18:33706651 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+23083C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706651 | |||||||
chr18:33706763 | T | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+23195T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706763 | |||||||
chr18:33706896 | C | G | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+23328C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706896 | |||||||
chr18:33706944 | G | A | 2 | a0006c0010t0015g0168 a0006c0010t0015g0184 |
2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+23376G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706944 | |||||||
chr18:33707111 | G | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+23543G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707111 | |||||||
chr18:33707129 | T | A | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+23561T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707129 | |||||||
chr18:33707149 | G | T | 1 | a0002c0002t0003g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.879+23581G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707149 | |||||||
chr18:33707374 | T | G | 1 | a0001c0005t0002g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.879+23806T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707374 | |||||||
chr18:33707428 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.879+23860C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707428 | |||||||
chr18:33707527 | AT | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.879+23966delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33707527 | ||||||
chr18:33707813 | A | T | 5 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-24155A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707813 | |||||||
chr18:33708008 | T | C | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-23960T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708008 | |||||||
chr18:33708041 | T | C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-23927T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708041 | |||||||
chr18:33708483 | A | G | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-23485A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708483 | |||||||
chr18:33708500 | T | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(186): Show |
190 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.880-23468T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708500 | |||||||
chr18:33708500 | T | G | 1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.880-23468T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708500 | |||||||
chr18:33708599 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(187): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.880-23369A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708599 | |||||||
chr18:33708603 | T | C | 138 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(135): Show |
139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.880-23365T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708603 | |||||||
chr18:33708650 | C | G | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-23318C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708650 | |||||||
chr18:33708940 | C | T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-23028C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708940 | |||||||
chr18:33708996 | A | G | 1 | a0001c0001t0008g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-22972A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708996 | |||||||
chr18:33709109 | A | C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22859A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709109 | |||||||
chr18:33709182 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.880-22786T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709182 | |||||||
chr18:33709224 | C | T | 1 | a0006c0025t0041g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.880-22744C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709224 | |||||||
chr18:33709301 | C | CA | 26 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(23): Show |
26 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22654dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33709301 | ||||||
chr18:33709301 | CA | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0070 a0001c0001t0002g0065 others(9): Show |
12 | HG01192.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-22654delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33709301 | ||||||
chr18:33709381 | A | T | 26 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22587A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709381 | |||||||
chr18:33709419 | T | C | 2 | a0001c0001t0002g0171 a0003c0003t0044g0215 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.880-22549T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709419 | |||||||
chr18:33709567 | TC | T | 2 | a0004c0004t0004g0214 a0015c0026t0036g0043 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.880-22400delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709567 | |||||||
chr18:33709627 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880-22341G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709627 | |||||||
chr18:33709640 | G | T | 41 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.880-22328G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709640 | |||||||
chr18:33709716 | A | G | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-22252A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709716 | |||||||
chr18:33709844 | T | A | 1 | a0002c0002t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.880-22124T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709844 | |||||||
chr18:33709877 | C | T | 87 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.880-22091C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709877 | |||||||
chr18:33709889 | T | C | 1 | a0001c0001t0006g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.880-22079T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709889 | |||||||
chr18:33709919 | A | T | 36 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(33): Show |
36 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.880-22049A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709919 | |||||||
chr18:33709978 | G | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-21990G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709978 | |||||||
chr18:33710096 | C | A | 192 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.880-21872C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710096 | |||||||
chr18:33710311 | T | C | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-21657T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710311 | |||||||
chr18:33710369 | C | G | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-21599C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710369 | |||||||
chr18:33710460 | T | G | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-21508T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710460 | |||||||
chr18:33710495 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.880-21473A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710495 | |||||||
chr18:33710626 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-21342A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710626 | |||||||
chr18:33710791 | A | T | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-21177A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710791 | |||||||
chr18:33710823 | A | G | 2 | a0001c0001t0006g0155 a0001c0001t0006g0157 |
2 | NA18959.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.880-21145A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710823 | |||||||
chr18:33710997 | T | C | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.880-20971T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710997 | |||||||
chr18:33711088 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-20880T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711088 | |||||||
chr18:33711348 | A | C | 27 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(24): Show |
27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.880-20620A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711348 | |||||||
chr18:33711765 | G | T | 3 | a0002c0002t0003g0078 a0002c0002t0004g0128 a0002c0002t0004g0129 |
3 | HG00642.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.880-20203G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711765 | |||||||
chr18:33711765 | GCTGTATT others(3): Show |
G | 1 | a0001c0001t0021g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.880-20202_880-2019 others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711765 | |||||||
chr18:33711832 | C | G | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-20136C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711832 | |||||||
chr18:33711847 | T | A | 7 | a0001c0001t0001g0070 a0001c0001t0002g0104 a0001c0001t0002g0122 others(4): Show |
7 | HG02735.hp2 HG02886.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-20121T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711847 | |||||||
chr18:33712200 | C | G | 10 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0002c0006t0007g0029 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-19768C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712200 | |||||||
chr18:33712424 | A | G | 2 | a0001c0001t0002g0171 a0003c0003t0044g0215 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.880-19544A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712424 | |||||||
chr18:33712484 | T | C | 192 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.880-19484T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712484 | |||||||
chr18:33712679 | GA | G | 5 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-19286delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33712679 | ||||||
chr18:33712757 | G | A | 3 | a0001c0001t0002g0065 a0001c0001t0002g0140 a0001c0001t0008g0033 |
3 | HG02109.hp2 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.880-19211G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712757 | |||||||
chr18:33712823 | A | G | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-19145A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712823 | |||||||
chr18:33712935 | C | T | 1 | a0003c0003t0009g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-19033C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712935 | |||||||
chr18:33712990 | C | T | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-18978C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712990 | |||||||
chr18:33713012 | A | G | 2 | a0002c0002t0004g0180 a0002c0002t0004g0181 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.880-18956A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713012 | |||||||
chr18:33713228 | GGTTTTTT others(12): Show |
G | 5 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0005g0016 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-18730_880-1871 others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713228 | ||||||
chr18:33713229 | G | GTTTT | 6 | a0001c0001t0001g0083 a0001c0001t0001g0205 a0001c0001t0002g0090 others(3): Show |
6 | HG01358.hp1 HG01981.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-18734_880-1873 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | G | GTTTTT | 5 | a0001c0001t0001g0126 a0001c0001t0002g0212 a0001c0001t0011g0213 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-18735_880-1873 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0005g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-18731_880-1873 others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | GTTTTTTT others(13): Show |
G | 3 | a0001c0017t0038g0174 a0009c0023t0032g0116 a0012c0022t0033g0118 |
3 | HG02818.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | GTTTTTTT others(14): Show |
G | 4 | a0001c0001t0001g0067 a0001c0001t0002g0183 a0001c0001t0028g0189 others(1): Show |
4 | HG01496.hp1 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-18730_880-1871 others(25): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | GTTTTTTT others(15): Show |
G | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-18730_880-1870 others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713229 | GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.880-18730_880-1870 others(27): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | ||||||
chr18:33713230 | TTTTTTTT others(11): Show |
T | 2 | a0001c0001t0005g0013 a0001c0001t0005g0014 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713230 | ||||||
chr18:33713231 | TTTTTTTG others(10): Show |
T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0015 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713231 | ||||||
chr18:33713232 | TTTTTTGT others(9): Show |
T | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713232 | ||||||
chr18:33713233 | TTTTTG | T | 9 | a0001c0001t0001g0086 a0001c0001t0001g0150 a0001c0001t0002g0007 others(6): Show |
9 | HG00438.hp1 HG01109.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-18720_880-1871 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713233 | ||||||
chr18:33713233 | TTTTTGTT others(8): Show |
T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713233 | ||||||
chr18:33713234 | TTTTG | T | 9 | a0001c0001t0001g0091 a0001c0001t0001g0119 a0001c0001t0001g0149 others(6): Show |
9 | HG00280.hp1 HG00642.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713234 | ||||||
chr18:33713234 | TTTTGTTT others(7): Show |
T | 2 | a0001c0001t0001g0175 a0001c0001t0009g0192 |
2 | HG02922.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713234 | ||||||
chr18:33713236 | TTG | T | 23 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(20): Show |
23 | HG00323.hp2 HG01255.hp1 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | ||||||
chr18:33713236 | TTGTTTTG | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0105 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | ||||||
chr18:33713236 | TTGTTTTG others(5): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | ||||||
chr18:33713237 | TG | T | 25 | a0001c0001t0001g0060 a0001c0001t0001g0099 a0001c0001t0001g0100 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.880-18730delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713237 | |||||||
chr18:33713237 | TGTTTTG | T | 8 | a0001c0001t0001g0049 a0001c0001t0001g0121 a0001c0001t0001g0131 others(5): Show |
8 | HG01361.hp1 HG02129.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713237 | |||||||
chr18:33713238 | G | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(61): Show |
64 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.880-18730G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713238 | |||||||
chr18:33713243 | G | T | 103 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0044 others(100): Show |
103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.880-18725G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713243 | |||||||
chr18:33713248 | G | GT | 7 | a0001c0001t0029g0164 a0001c0008t0017g0025 a0002c0002t0003g0054 others(4): Show |
7 | HG00735.hp2 HG00741.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-18694dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713248 | ||||||
chr18:33713248 | G | T | 122 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(119): Show |
123 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.880-18720G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713248 | |||||||
chr18:33713249 | T | TTTTG | 8 | a0001c0001t0002g0123 a0001c0001t0002g0140 a0002c0002t0004g0167 others(5): Show |
8 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-18716_880-1871 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713249 | ||||||
chr18:33713250 | T | TTTG | 29 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0002g0065 others(26): Show |
29 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.880-18716_880-1871 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713250 | ||||||
chr18:33713253 | T | G | 5 | a0002c0002t0004g0181 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02965.hp1 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-18715T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713253 | |||||||
chr18:33713254 | T | G | 2 | a0003c0003t0009g0011 a0006c0025t0041g0005 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.880-18714T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713254 | |||||||
chr18:33713259 | T | G | 1 | a0003c0003t0009g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-18709T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713259 | |||||||
chr18:33713265 | T | G | 6 | a0004c0004t0004g0045 a0004c0004t0004g0058 a0004c0004t0004g0059 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-18703T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713265 | |||||||
chr18:33713273 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.880-18695T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713273 | |||||||
chr18:33713299 | G | GGC | 21 | a0001c0001t0001g0141 a0001c0001t0001g0206 a0001c0001t0001g0207 others(18): Show |
21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-18668_880-1866 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713299 | ||||||
chr18:33713312 | T | C | 1 | a0002c0002t0003g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.880-18656T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713312 | |||||||
chr18:33713341 | A | ACCCCCCC | 12 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0090 others(9): Show |
12 | HG01071.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-18624_880-1861 others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713341 | ||||||
chr18:33713344 | C | CCG | 119 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(116): Show |
120 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.880-18623_880-1862 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713344 | ||||||
chr18:33713348 | C | CCT | 24 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(21): Show |
24 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-18619_880-1861 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713348 | ||||||
chr18:33713348 | C | T | 1 | a0002c0002t0004g0161 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.880-18620C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713348 | |||||||
chr18:33713360 | T | C | 192 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.880-18608T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713360 | |||||||
chr18:33713535 | G | A | 108 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(105): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.880-18433G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713535 | |||||||
chr18:33713595 | A | G | 1 | a0001c0001t0018g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.880-18373A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713595 | |||||||
chr18:33713685 | C | T | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-18283C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713685 | |||||||
chr18:33713828 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(137): Show |
141 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.880-18140C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713828 | |||||||
chr18:33713943 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.880-18025A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713943 | |||||||
chr18:33714017 | G | A | 111 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(108): Show |
112 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.880-17951G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714017 | |||||||
chr18:33714246 | G | A | 3 | a0001c0008t0017g0025 a0002c0006t0007g0026 a0005c0024t0005g0027 |
3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.880-17722G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714246 | |||||||
chr18:33714297 | G | A | 194 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(191): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.880-17671G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714297 | |||||||
chr18:33714662 | C | T | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-17306C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714662 | |||||||
chr18:33714711 | T | C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-17257T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714711 | |||||||
chr18:33714816 | T | G | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-17152T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714816 | |||||||
chr18:33714970 | T | G | 1 | a0001c0001t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.880-16998T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714970 | |||||||
chr18:33715036 | T | C | 192 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(189): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.880-16932T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715036 | |||||||
chr18:33715080 | A | G | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.880-16888A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715080 | |||||||
chr18:33715304 | G | A | 139 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(136): Show |
140 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.880-16664G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715304 | |||||||
chr18:33715350 | A | G | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.880-16618A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715350 | |||||||
chr18:33715649 | A | G | 3 | a0003c0003t0013g0006 a0003c0003t0013g0010 a0003c0003t0037g0009 |
3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880-16319A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715649 | |||||||
chr18:33716227 | G | A | 1 | a0002c0002t0004g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-15741G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716227 | |||||||
chr18:33716271 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-15697G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716271 | |||||||
chr18:33716482 | G | A | 1 | a0009c0023t0032g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.880-15486G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716482 | |||||||
chr18:33716518 | G | A | 1 | a0002c0002t0003g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.880-15450G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716518 | |||||||
chr18:33716650 | G | A | 5 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(2): Show |
5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-15318G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716650 | |||||||
chr18:33716894 | G | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-15074G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716894 | |||||||
chr18:33716897 | T | TA | 173 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(170): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.880-15056dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33716897 | ||||||
chr18:33716897 | T | TAA | 16 | a0001c0001t0001g0044 a0001c0008t0017g0025 a0002c0006t0007g0026 others(13): Show |
16 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.880-15057_880-1505 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33716897 | ||||||
chr18:33716950 | T | A | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-15018T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716950 | |||||||
chr18:33717041 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-14927A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717041 | |||||||
chr18:33717090 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-14878G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717090 | |||||||
chr18:33717117 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-14851T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717117 | |||||||
chr18:33717520 | C | T | 25 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(22): Show |
25 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.880-14448C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717520 | |||||||
chr18:33717806 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880-14162A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717806 | |||||||
chr18:33717856 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(8): Show |
11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-14112C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717856 | |||||||
chr18:33717882 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0005g0034 a0001c0001t0005g0035 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-14086C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717882 | |||||||
chr18:33717900 | T | C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0014g0053 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-14068T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717900 | |||||||
chr18:33718131 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0018t0001g0069 |
3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.880-13837G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718131 | |||||||
chr18:33718150 | T | TAAGTTCC others(835): Show |
1 | a0001c0001t0001g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.880-13802_880-1380 others(846): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33718150 | ||||||
chr18:33718345 | G | A | 2 | a0007c0009t0002g0158 a0007c0009t0002g0159 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.880-13623G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718345 | |||||||
chr18:33718367 | T | C | 23 | a0001c0001t0001g0092 a0001c0001t0001g0141 a0001c0001t0001g0206 others(20): Show |
23 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-13601T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718367 | |||||||
chr18:33718537 | C | T | 4 | a0001c0001t0006g0082 a0001c0001t0006g0085 a0001c0001t0006g0191 others(1): Show |
4 | HG00438.hp1 HG02129.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-13431C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718537 | |||||||
chr18:33718566 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-13402A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718566 | |||||||
chr18:33718581 | A | G | 2 | a0002c0002t0004g0180 a0002c0002t0004g0181 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.880-13387A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718581 | |||||||
chr18:33718594 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0012g0187 |
3 | HG01070.hp1 HG01071.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.880-13374C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718594 | |||||||
chr18:33718959 | A | G | 93 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0041 others(90): Show |
93 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.880-13009A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718959 | |||||||
chr18:33719213 | A | C | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-12755A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719213 | |||||||
chr18:33719338 | T | C | 13 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(10): Show |
13 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-12630T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719338 | |||||||
chr18:33719409 | T | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-12559T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719409 | |||||||
chr18:33719629 | A | G | 1 | a0001c0018t0001g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.880-12339A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719629 | |||||||
chr18:33719884 | T | C | 1 | a0012c0022t0033g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.880-12084T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719884 | |||||||
chr18:33719964 | A | G | 18 | a0001c0001t0001g0070 a0001c0001t0002g0065 a0001c0001t0002g0104 others(15): Show |
19 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-12004A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719964 | |||||||
chr18:33720289 | AG | A | 12 | a0001c0001t0001g0055 a0001c0001t0005g0012 a0001c0001t0005g0013 others(9): Show |
13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.880-11678delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720289 | |||||||
chr18:33720381 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.880-11587A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720381 | |||||||
chr18:33720391 | A | G | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.880-11577A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720391 | |||||||
chr18:33720595 | G | A | 166 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(163): Show |
166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.880-11373G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720595 | |||||||
chr18:33720981 | CT | C | 18 | a0001c0001t0001g0160 a0002c0002t0004g0075 a0002c0002t0004g0080 others(15): Show |
18 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-10984delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33720981 | ||||||
chr18:33721029 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-10939A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721029 | |||||||
chr18:33721231 | A | G | 18 | a0001c0001t0001g0160 a0002c0002t0004g0075 a0002c0002t0004g0080 others(15): Show |
18 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-10737A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721231 | |||||||
chr18:33721259 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0001g0147 |
3 | HG00323.hp2 HG00735.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.880-10709G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721259 | |||||||
chr18:33721404 | G | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(1): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-10564G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721404 | |||||||
chr18:33721409 | T | C | 31 | a0001c0001t0002g0007 a0001c0001t0002g0065 a0001c0001t0002g0104 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-10559T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721409 | |||||||
chr18:33721410 | A | C | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-10558A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721410 | |||||||
chr18:33721631 | A | G | 6 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-10337A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721631 | |||||||
chr18:33721739 | G | C | 3 | a0001c0017t0038g0174 a0003c0003t0009g0172 a0003c0003t0009g0173 |
3 | HG02258.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880-10229G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721739 | |||||||
chr18:33721940 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | HG02602.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.880-10028A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721940 | |||||||
chr18:33722086 | G | A | 9 | a0001c0001t0002g0171 a0001c0001t0011g0137 a0001c0001t0011g0213 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-9882G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722086 | |||||||
chr18:33722153 | G | A | 31 | a0001c0001t0002g0007 a0001c0001t0002g0065 a0001c0001t0002g0104 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-9815G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722153 | |||||||
chr18:33722489 | C | T | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-9479C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722489 | |||||||
chr18:33722574 | G | A | 9 | a0001c0001t0042g0182 a0002c0002t0003g0106 a0002c0002t0003g0108 others(6): Show |
9 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-9394G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722574 | |||||||
chr18:33722726 | A | G | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.880-9242A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722726 | |||||||
chr18:33723019 | C | T | 1 | a0015c0026t0036g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.880-8949C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723019 | |||||||
chr18:33723369 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.880-8599G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723369 | |||||||
chr18:33723542 | G | A | 2 | a0002c0002t0004g0080 a0002c0013t0027g0079 |
2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.880-8426G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723542 | |||||||
chr18:33723593 | C | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(98): Show |
101 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.880-8375C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723593 | |||||||
chr18:33723679 | A | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(168): Show |
172 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.880-8289A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723679 | |||||||
chr18:33723905 | C | T | 1 | a0002c0002t0004g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.880-8063C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723905 | |||||||
chr18:33724073 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-7895G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724073 | |||||||
chr18:33724198 | T | A | 3 | a0001c0017t0038g0174 a0003c0003t0009g0172 a0003c0003t0009g0173 |
3 | HG02258.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880-7770T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724198 | |||||||
chr18:33724242 | A | C | 31 | a0001c0001t0002g0007 a0001c0001t0002g0065 a0001c0001t0002g0104 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-7726A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724242 | |||||||
chr18:33724354 | G | T | 151 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
152 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.880-7614G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724354 | |||||||
chr18:33724457 | C | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
152 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.880-7511C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724457 | |||||||
chr18:33724574 | G | C | 5 | a0001c0005t0002g0002 a0001c0005t0002g0061 a0001c0005t0002g0165 others(2): Show |
5 | HG00621.hp2 NA18998.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-7394G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724574 | |||||||
chr18:33724589 | G | A | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-7379G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724589 | |||||||
chr18:33724949 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0005g0021 a0001c0001t0022g0073 |
3 | HG02559.hp1 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.880-7019C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724949 | |||||||
chr18:33725010 | C | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(78): Show |
81 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.880-6958C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725010 | |||||||
chr18:33725330 | A | G | 1 | a0010c0014t0047g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-6638A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725330 | |||||||
chr18:33725490 | A | G | 19 | a0001c0001t0042g0182 a0001c0017t0038g0174 a0002c0002t0003g0106 others(16): Show |
19 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-6478A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725490 | |||||||
chr18:33725615 | T | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(1): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-6353T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725615 | |||||||
chr18:33725617 | T | C | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-6351T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725617 | |||||||
chr18:33725643 | C | A | 1 | a0002c0002t0003g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-6325C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725643 | |||||||
chr18:33725848 | C | T | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | NA18948.hp2 NA18970.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.880-6120C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725848 | |||||||
chr18:33726416 | C | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0188 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.880-5552C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726416 | |||||||
chr18:33726781 | C | T | 31 | a0001c0001t0002g0007 a0001c0001t0002g0065 a0001c0001t0002g0104 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-5187C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726781 | |||||||
chr18:33726869 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-5099C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726869 | |||||||
chr18:33727083 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880-4885C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727083 | |||||||
chr18:33727446 | A | G | 2 | a0003c0003t0009g0172 a0003c0003t0009g0173 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-4522A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727446 | |||||||
chr18:33727456 | G | T | 152 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(149): Show |
153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.880-4512G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727456 | |||||||
chr18:33727591 | C | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-4377C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727591 | |||||||
chr18:33727804 | G | A | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-4164G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727804 | |||||||
chr18:33728028 | C | G | 1 | a0002c0002t0004g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.880-3940C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728028 | |||||||
chr18:33728325 | T | A | 1 | a0001c0017t0038g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-3643T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728325 | |||||||
chr18:33728558 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.880-3410C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728558 | |||||||
chr18:33728768 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.880-3200C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728768 | |||||||
chr18:33728816 | T | C | 3 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 |
3 | NA18943.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.880-3152T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728816 | |||||||
chr18:33729070 | T | C | 1 | a0002c0006t0007g0026 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.880-2898T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729070 | |||||||
chr18:33729115 | G | GAAAC | 16 | a0001c0001t0042g0182 a0002c0002t0003g0106 a0002c0002t0003g0108 others(13): Show |
16 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.880-2851_880-2848d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33729115 | ||||||
chr18:33729169 | G | C | 102 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(99): Show |
102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.880-2799G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729169 | |||||||
chr18:33729351 | G | A | 1 | a0013c0015t0001g0115 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.880-2617G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729351 | |||||||
chr18:33729573 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-2395G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729573 | |||||||
chr18:33729719 | CTCA | C | 3 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 |
3 | NA18943.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.880-2243_880-2241d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33729719 | ||||||
chr18:33729726 | T | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-2242T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729726 | |||||||
chr18:33729758 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.880-2210T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729758 | |||||||
chr18:33729819 | C | T | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-2149C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729819 | |||||||
chr18:33730002 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.880-1966C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730002 | |||||||
chr18:33730025 | C | G | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1943C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730025 | |||||||
chr18:33730216 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.880-1752C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730216 | |||||||
chr18:33730298 | C | G | 32 | a0001c0001t0002g0007 a0001c0001t0002g0065 a0001c0001t0002g0104 others(29): Show |
32 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-1670C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730298 | |||||||
chr18:33730317 | G | A | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-1651G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730317 | |||||||
chr18:33730452 | C | T | 153 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(150): Show |
154 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.880-1516C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730452 | |||||||
chr18:33730556 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-1412A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730556 | |||||||
chr18:33730602 | G | A | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1366G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730602 | |||||||
chr18:33730611 | T | TGGCATGG others(17): Show |
1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-1356_880-1333d others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33730611 | ||||||
chr18:33730797 | T | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(98): Show |
101 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.880-1171T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730797 | |||||||
chr18:33730976 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-992C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730976 | |||||||
chr18:33731020 | T | TCTTTGCT others(23): Show |
1 | a0001c0001t0002g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.880-944_880-915dup others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33731020 | ||||||
chr18:33731123 | G | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-845G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731123 | |||||||
chr18:33731197 | G | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(98): Show |
101 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.880-771G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731197 | |||||||
chr18:33731210 | C | CA | 86 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.880-752dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33731210 | ||||||
chr18:33731234 | CTA | C | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-733_880-732del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731234 | |||||||
chr18:33731352 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.880-616T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731352 | |||||||
chr18:33731414 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.880-554C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731414 | |||||||
chr18:33731416 | G | A | 1 | a0015c0026t0036g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.880-552G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731416 | |||||||
chr18:33731498 | C | T | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-470C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731498 | |||||||
chr18:33731556 | G | A | 9 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0002c0006t0007g0026 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-412G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731556 | |||||||
chr18:33731639 | A | T | 16 | a0001c0001t0001g0055 a0001c0001t0002g0007 a0001c0001t0002g0171 others(13): Show |
17 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.880-329A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731639 | |||||||
chr18:33731660 | C | T | 1 | a0003c0003t0013g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.880-308C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731660 | |||||||
chr18:33731952 | C | T | 1 | a0001c0005t0002g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.880-16C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731952 | |||||||
chr18:33732105 | A | G | 1 | a0001c0001t0014g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.976+41A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732105 | |||||||
chr18:33732142 | T | C | 192 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(189): Show |
193 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.976+78T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732142 | |||||||
chr18:33732184 | A | G | 154 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(151): Show |
155 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.976+120A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732184 | |||||||
chr18:33732435 | C | T | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.976+371C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732435 | |||||||
chr18:33732439 | T | C | 6 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.976+375T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732439 | |||||||
chr18:33732489 | T | C | 31 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0002g0122 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.976+425T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732489 | |||||||
chr18:33732774 | G | T | 167 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(164): Show |
168 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.976+710G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732774 | |||||||
chr18:33732821 | A | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG00642.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.976+757A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732821 | |||||||
chr18:33732860 | CA | C | 61 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0002g0007 others(58): Show |
62 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.976+815delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33732860 | ||||||
chr18:33732860 | CAA | C | 107 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(104): Show |
107 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.976+814_976+815del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33732860 | ||||||
chr18:33732882 | A | G | 17 | a0001c0001t0002g0051 a0001c0001t0002g0090 a0001c0001t0002g0152 others(14): Show |
17 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.976+818A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732882 | |||||||
chr18:33733160 | G | T | 151 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
152 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.976+1096G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733160 | |||||||
chr18:33733338 | T | C | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.977-972T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733338 | |||||||
chr18:33733382 | T | C | 47 | a0001c0001t0002g0183 a0001c0001t0035g0098 a0001c0017t0038g0174 others(44): Show |
47 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.977-928T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733382 | |||||||
chr18:33733430 | A | G | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-880A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733430 | |||||||
chr18:33733747 | CA | C | 5 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-559delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33733747 | ||||||
chr18:33733751 | A | G | 5 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-559A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733751 | |||||||
chr18:33733753 | A | G | 5 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-557A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733753 | |||||||
chr18:33733791 | T | C | 1 | a0011c0012t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.977-519T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733791 | |||||||
chr18:33733802 | T | G | 24 | a0001c0001t0035g0098 a0002c0002t0004g0075 a0002c0002t0004g0080 others(21): Show |
24 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.977-508T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733802 | |||||||
chr18:33733856 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.977-454G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733856 | |||||||
chr18:33733863 | C | T | 1 | a0001c0001t0031g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.977-447C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733863 | |||||||
chr18:33733869 | C | T | 1 | a0003c0003t0009g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.977-441C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733869 | |||||||
chr18:33733901 | A | G | 1 | a0002c0002t0046g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.977-409A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733901 | |||||||
chr18:33733915 | T | G | 1 | a0001c0001t0028g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.977-395T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733915 | |||||||
chr18:33733935 | G | A | 2 | a0001c0001t0002g0183 a0016c0019t0034g0003 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.977-375G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733935 | |||||||
chr18:33734000 | C | T | 27 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0002g0122 others(24): Show |
27 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.977-310C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734000 | |||||||
chr18:33734001 | G | T | 148 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(145): Show |
149 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.977-309G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734001 | |||||||
chr18:33734039 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.977-271C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734039 | |||||||
chr18:33734044 | T | TGCTTTAG others(19): Show |
146 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(143): Show |
146 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.977-202_977-177dup others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | ||||||
chr18:33734044 | T | TGCTTTAG others(45): Show |
25 | a0001c0001t0001g0055 a0001c0001t0001g0091 a0001c0001t0002g0007 others(22): Show |
26 | HG00642.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.977-228_977-177dup others(52): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | ||||||
chr18:33734044 | TGCTTTAG others(19): Show |
T | 10 | a0001c0001t0042g0182 a0001c0005t0002g0163 a0002c0002t0003g0106 others(7): Show |
10 | HG00280.hp2 HG00558.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.977-202_977-177del others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | ||||||
chr18:33734194 | T | C | 5 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 others(2): Show |
5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-116T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734194 | |||||||
chr18:33734232 | A | G | 149 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(146): Show |
150 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.977-78A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734232 | |||||||
chr18:33734425 | A | T | 13 | a0001c0001t0002g0090 a0001c0001t0002g0152 a0001c0001t0002g0196 others(10): Show |
13 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+10A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734425 | |||||||
chr18:33734471 | C | T | 13 | a0001c0001t0002g0090 a0001c0001t0002g0152 a0001c0001t0002g0196 others(10): Show |
13 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+56C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734471 | |||||||
chr18:33734757 | T | C | 85 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(82): Show |
85 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1082+342T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734757 | |||||||
chr18:33734959 | G | T | 1 | a0002c0006t0043g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1082+544G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734959 | |||||||
chr18:33735005 | A | G | 1 | a0002c0006t0043g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1082+590A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735005 | |||||||
chr18:33735376 | A | G | 21 | a0001c0001t0042g0182 a0001c0008t0017g0025 a0001c0008t0040g0219 others(18): Show |
21 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082+961A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735376 | |||||||
chr18:33735488 | A | T | 1 | a0003c0003t0009g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1082+1073A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735488 | |||||||
chr18:33735709 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0076 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1082+1294A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735709 | |||||||
chr18:33735772 | AT | A | 27 | a0001c0001t0002g0065 a0001c0001t0002g0104 a0001c0001t0002g0122 others(24): Show |
27 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1082+1363delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33735772 | ||||||
chr18:33735822 | C | T | 8 | a0002c0002t0003g0106 a0002c0002t0003g0108 a0002c0002t0003g0109 others(5): Show |
8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082+1407C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735822 | |||||||
chr18:33735914 | G | C | 116 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(113): Show |
117 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1082+1499G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735914 | |||||||
chr18:33736003 | TATTTC | T | 154 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(151): Show |
155 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.1082+1593_1082+159 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736003 | ||||||
chr18:33736006 | T | C | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1082+1591T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736006 | |||||||
chr18:33736116 | C | A | 13 | a0001c0001t0042g0182 a0001c0008t0017g0025 a0001c0008t0040g0219 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+1701C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736116 | |||||||
chr18:33736205 | C | T | 106 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(103): Show |
106 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1082+1790C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736205 | |||||||
chr18:33736260 | G | C | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1082+1845G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736260 | |||||||
chr18:33736328 | C | A | 6 | a0002c0006t0007g0029 a0002c0006t0007g0030 a0002c0006t0007g0031 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082+1913C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736328 | |||||||
chr18:33736345 | C | CT | 6 | a0003c0003t0009g0011 a0003c0003t0013g0006 a0003c0003t0013g0010 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082+1938dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736345 | ||||||
chr18:33736345 | C | CTTT | 19 | a0001c0001t0002g0065 a0001c0001t0002g0122 a0001c0001t0002g0123 others(16): Show |
19 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1082+1936_1082+193 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736345 | ||||||
chr18:33736445 | C | T | 1 | a0002c0006t0007g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1082+2030C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736445 | |||||||
chr18:33736744 | T | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(83): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1083-1743T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736744 | |||||||
chr18:33736782 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0018 a0001c0001t0008g0020 others(1): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083-1705G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736782 | |||||||
chr18:33736933 | T | C | 2 | a0009c0023t0032g0116 a0012c0022t0033g0118 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1083-1554T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736933 | |||||||
chr18:33737178 | C | A | 1 | a0001c0001t0002g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083-1309C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737178 | |||||||
chr18:33737520 | G | A | 3 | a0002c0006t0043g0101 a0009c0023t0032g0116 a0012c0022t0033g0118 |
3 | HG02818.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1083-967G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737520 | |||||||
chr18:33737624 | A | G | 4 | a0001c0001t0042g0182 a0002c0006t0043g0101 a0009c0023t0032g0116 others(1): Show |
4 | HG02818.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083-863A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737624 | |||||||
chr18:33737791 | A | G | 170 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(167): Show |
171 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1083-696A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737791 | |||||||
chr18:33737854 | C | G | 11 | a0001c0001t0042g0182 a0002c0006t0007g0026 a0002c0006t0007g0029 others(8): Show |
11 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083-633C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737854 | |||||||
chr18:33737953 | T | G | 1 | a0001c0001t0005g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1083-534T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737953 | |||||||
chr18:33737972 | G | A | 2 | a0001c0001t0011g0137 a0001c0001t0011g0213 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1083-515G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737972 | |||||||
chr18:33738039 | G | A | 1 | a0002c0002t0003g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1083-448G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738039 | |||||||
chr18:33738122 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1083-365G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738122 | |||||||
chr18:33738218 | T | C | 7 | a0002c0006t0007g0026 a0002c0006t0007g0029 a0002c0006t0007g0030 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083-269T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738218 | |||||||
chr18:33738237 | C | T | 3 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 |
3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1083-250C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738237 | |||||||
chr18:33738290 | C | T | 7 | a0002c0006t0007g0026 a0002c0006t0007g0029 a0002c0006t0007g0030 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083-197C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738290 | |||||||
chr18:33738292 | G | C | 158 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(155): Show |
159 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083-195G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738292 | |||||||
chr18:33738334 | A | T | 1 | a0001c0001t0029g0164 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1083-153A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738334 | |||||||
chr18:33738372 | T | C | 152 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(149): Show |
153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1083-115T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738372 | |||||||
chr18:33738412 | A | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(148): Show |
152 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.1083-75A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738412 | |||||||
chr18:33740574 | T | C | 1 | a0001c0001t0005g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3039+131T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740574 | |||||||
chr18:33740716 | G | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3039+273G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740716 | |||||||
chr18:33740752 | A | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(98): Show |
101 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.3039+309A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740752 | |||||||
chr18:33740850 | GCTCT | G | 7 | a0003c0003t0009g0011 a0003c0003t0009g0172 a0003c0003t0009g0173 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3039+410_3039+413d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 33740850 | ||||||
chr18:33741325 | A | T | 163 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(160): Show |
164 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.3039+882A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741325 | |||||||
chr18:33741687 | A | G | 1 | a0001c0001t0042g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3040-1201A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741687 | |||||||
chr18:33741731 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3040-1157A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741731 | |||||||
chr18:33741853 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0005g0022 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3040-1035G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741853 | |||||||
chr18:33742030 | C | T | 16 | a0002c0002t0004g0075 a0002c0002t0004g0080 a0002c0002t0004g0120 others(13): Show |
16 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3040-858C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742030 | |||||||
chr18:33742085 | G | A | 2 | a0002c0002t0004g0080 a0002c0013t0027g0079 |
2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3040-803G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742085 | |||||||
chr18:33742241 | G | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3040-647G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742241 | |||||||
chr18:33742314 | A | G | 164 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(161): Show |
165 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.3040-574A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742314 | |||||||
chr18:33742397 | A | AAAGT | 3 | a0001c0008t0017g0025 a0001c0008t0040g0219 a0001c0017t0038g0174 |
3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3040-490_3040-487d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 33742397 | ||||||
chr18:33742444 | C | T | 2 | a0001c0005t0002g0061 a0001c0005t0020g0062 |
2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3040-444C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742444 | |||||||
chr18:33742576 | T | C | 164 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0040 others(161): Show |
165 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.3040-312T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742576 | |||||||
chr18:33742666 | T | A | 1 | a0003c0003t0044g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3040-222T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742666 | |||||||
chr18:33742688 | T | C | 1 | a0007c0009t0002g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3040-200T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742688 | |||||||
chr18:33742843 | T | G | 2 | a0002c0002t0004g0080 a0002c0013t0027g0079 |
2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3040-45T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742843 |