Item | Value |
---|---|
geneid | 1063 |
ensemblid | ENSG00000117724.15 |
hgncid | 1857 |
symbol | CENPF |
name | centromere protein F |
refseq_nuc | NM_016343.4 |
refseq_prot | NP_057427.3 |
ensembl_nuc | ENST00000366955.8 |
ensembl_prot | ENSP00000355922.3 |
mane_status | MANE Select |
chr | chr1 |
start | 214603195 |
end | 214664571 |
strand | + |
ver | v1.2 |
region | chr1:214603195-214664571 |
region5000 | chr1:214598195-214669571 |
regionname0 | CENPF_chr1_214603195_214664571 |
regionname5000 | CENPF_chr1_214598195_214669571 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 3114 | 81 | 7 | 16 | 42 | 4 | 12 | 28 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0002 | 0/1 | 3114 | 35 | 1 | 9 | 10 | 4 | 10 | 9 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0003 | 0/0 | 3114 | 27 | 0 | 5 | 17 | 0 | 5 | 13 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0004 | 0/0 | 3114 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0005 | 0/0 | 3114 | 15 | 1 | 4 | 9 | 0 | 1 | 8 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0006 | 0/0 | 3114 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0007 | 1/0 | 3114 | 9 | 6 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0008 | 0/0 | 3114 | 8 | 2 | 1 | 4 | 1 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0009 | 0/0 | 3114 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0010 | 0/0 | 3114 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0011 | 0/0 | 3114 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0012 | 0/0 | 3114 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0013 | 0/0 | 3114 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0014 | 0/0 | 3114 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0015 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0016 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0017 | 0/0 | 3114 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0018 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0019 | 0/0 | 3114 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0020 | 0/0 | 3114 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0021 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0022 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0023 | 0/0 | 3114 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0024 | 0/0 | 3114 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0025 | 0/0 | 3114 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0026 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0027 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0028 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0029 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0030 | 0/0 | 3114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0031 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0032 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0033 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0034 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0035 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0036 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0037 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0038 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0039 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0040 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0041 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0042 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0043 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0044 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0045 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0046 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0047 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0048 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0049 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
a0050 | 0/0 | 3114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | MSWAL others(3109): Show |
chr1 | 214598195 | 214669571 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 9342 | 73 | 7 | 16 | 39 | 4 | 7 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0001c0011 | 0/0 | 9342 | 4 | 0 | 0 | 0 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0001c0017 | 0/0 | 9342 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0001c0042 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0002c0002 | 0/1 | 9342 | 34 | 1 | 8 | 10 | 4 | 10 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0002c0032 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0003c0003 | 0/0 | 9342 | 26 | 0 | 5 | 17 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0003c0059 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0004c0004 | 0/0 | 9342 | 16 | 15 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0004c0013 | 0/0 | 9342 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0004c0033 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0005c0005 | 0/0 | 9342 | 15 | 1 | 4 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0006c0007 | 0/0 | 9342 | 8 | 8 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0006c0030 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0007c0009 | 1/0 | 9342 | 5 | 2 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0007c0012 | 0/0 | 9342 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0008c0006 | 0/0 | 9342 | 8 | 2 | 1 | 4 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0009c0010 | 0/0 | 9342 | 5 | 5 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0010c0008 | 0/0 | 9342 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0011c0014 | 0/0 | 9342 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0012c0015 | 0/0 | 9342 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0013c0018 | 0/0 | 9342 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0013c0034 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0014c0016 | 0/0 | 9342 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0015c0024 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0015c0055 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0016c0029 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0016c0052 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0017c0020 | 0/0 | 9342 | 3 | 1 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0018c0019 | 0/0 | 9342 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0019c0022 | 0/0 | 9342 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0020c0027 | 0/0 | 9342 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0021c0028 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0022c0025 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0023c0023 | 0/0 | 9342 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0024c0026 | 0/0 | 9342 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0025c0021 | 0/0 | 9342 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0026c0044 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0027c0039 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0028c0031 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0029c0045 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0030c0057 | 0/0 | 9342 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0031c0056 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0032c0035 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0033c0049 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0034c0036 | 0/0 | 9342 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0035c0061 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0036c0051 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0037c0053 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0038c0058 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0039c0047 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0040c0046 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0041c0041 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0042c0062 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0043c0043 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0044c0038 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0045c0050 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0046c0048 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0047c0054 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0048c0037 | 0/0 | 9342 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0049c0060 | 0/0 | 9342 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 | ||
a0050c0040 | 0/0 | 9342 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | ATGAG others(9337): Show |
chr1 | 214598195 | 214669571 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10290 | 70 | 7 | 16 | 36 | 4 | 7 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0001t0008 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0001t0009 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0001t0011 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0011t0001 | 0/0 | 10290 | 4 | 0 | 0 | 0 | 0 | 4 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0017t0001 | 0/0 | 10290 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0001c0042t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0002c0002t0001 | 0/1 | 10290 | 25 | 1 | 6 | 7 | 4 | 6 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0002c0002t0002 | 0/0 | 10290 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0002c0002t0005 | 0/0 | 10290 | 4 | 0 | 1 | 0 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0002c0002t0007 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0002c0032t0001 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0003c0003t0002 | 0/0 | 10290 | 25 | 0 | 5 | 17 | 0 | 3 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0003c0003t0013 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0003c0059t0002 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0004c0004t0002 | 0/0 | 10290 | 16 | 15 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0004c0013t0002 | 0/0 | 10290 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0004c0033t0002 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0005c0005t0003 | 0/0 | 10290 | 15 | 1 | 4 | 9 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0006c0007t0002 | 0/0 | 10290 | 8 | 8 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0006c0030t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0007c0009t0001 | 1/0 | 10290 | 5 | 2 | 0 | 1 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0007c0012t0001 | 0/0 | 10290 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0008c0006t0001 | 0/0 | 10290 | 8 | 2 | 1 | 4 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0009c0010t0001 | 0/0 | 10290 | 5 | 5 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0010c0008t0001 | 0/0 | 10290 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0011c0014t0002 | 0/0 | 10290 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0012c0015t0004 | 0/0 | 10290 | 4 | 3 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0013c0018t0002 | 0/0 | 10290 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0013c0034t0014 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0014c0016t0001 | 0/0 | 10290 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0015c0024t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0015c0055t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0016c0029t0004 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0016c0052t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0017c0020t0006 | 0/0 | 10290 | 3 | 1 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0018c0019t0001 | 0/0 | 10290 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0019c0022t0001 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0020c0027t0001 | 0/0 | 10290 | 2 | 0 | 1 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0021c0028t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0022c0025t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0022c0025t0012 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0023c0023t0001 | 0/0 | 10290 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0024c0026t0002 | 0/0 | 10290 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0025c0021t0001 | 0/0 | 10290 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0026c0044t0003 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0027c0039t0001 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0028c0031t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0029c0045t0003 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0030c0057t0002 | 0/0 | 10290 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0031c0056t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0032c0035t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0033c0049t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0034c0036t0001 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0035c0061t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0036c0051t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0037c0053t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0038c0058t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0039c0047t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0040c0046t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0041c0041t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0042c0062t0001 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0043c0043t0006 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0044c0038t0001 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0045c0050t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0046c0048t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0047c0054t0002 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0048c0037t0001 | 0/0 | 10290 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0049c0060t0004 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
a0050c0040t0010 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | AGAAG others(10285): Show |
chr1 | 214598195 | 214669571 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0011 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0001t0011g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0011t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0017t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0017t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0001c0042t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0007g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0002t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0002c0032t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0002 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0003t0013g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0003c0059t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0004t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0013t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0004c0033t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0005c0005t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0007t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0006c0030t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0012t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0007c0012t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0008c0006t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0009c0010t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0010c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0014t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0014t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0014t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0011c0014t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0015t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0015t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0015t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0012c0015t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0018t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0018t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0018t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0013c0034t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0014c0016t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0015c0024t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0015c0055t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0029t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0029t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0016c0052t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0020t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0020t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0017c0020t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0019t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0019t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0018c0019t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0019c0022t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0019c0022t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0020c0027t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0020c0027t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0021c0028t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0021c0028t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0022c0025t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0022c0025t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0023c0023t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0023c0023t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0024c0026t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0024c0026t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0025c0021t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0025c0021t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0026c0044t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0027c0039t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0028c0031t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0029c0045t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0030c0057t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0031c0056t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0032c0035t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0033c0049t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0034c0036t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0035c0061t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0036c0051t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0037c0053t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0038c0058t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0039c0047t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0040c0046t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0041c0041t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0042c0062t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0043c0043t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0044c0038t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0045c0050t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0046c0048t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0047c0054t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0048c0037t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0049c0060t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
a0050c0040t0010g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0093 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | GBR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00323 | hp2 | a0019 | c0022 | t0001 | g0109 | EUR | FIN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00408 | hp2 | a0003 | c0003 | t0002 | g0073 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0172 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0104 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00642 | hp1 | a0002 | c0032 | t0001 | g0110 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00642 | hp2 | a0004 | c0033 | t0002 | g0039 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00673 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01074 | hp1 | a0003 | c0003 | t0002 | g0065 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01081 | hp2 | a0020 | c0027 | t0001 | g0121 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01106 | hp1 | a0011 | c0014 | t0002 | g0034 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01109 | hp1 | a0004 | c0004 | t0002 | g0189 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01109 | hp2 | a0012 | c0015 | t0004 | g0054 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0002 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01192 | hp2 | a0014 | c0016 | t0001 | g0007 | AMR | PUR | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01257 | hp2 | a0003 | c0003 | t0002 | g0074 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01346 | hp2 | a0005 | c0005 | t0003 | g0216 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01358 | hp1 | a0026 | c0044 | t0003 | g0206 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01433 | hp1 | a0027 | c0039 | t0001 | g0007 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01433 | hp2 | a0002 | c0002 | t0007 | g0103 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01496 | hp1 | a0005 | c0005 | t0003 | g0012 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0108 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01515 | hp2 | a0028 | c0031 | t0001 | g0175 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01891 | hp1 | a0006 | c0007 | t0002 | g0050 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01891 | hp2 | a0013 | c0034 | t0014 | g0041 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01928 | hp2 | a0005 | c0005 | t0003 | g0012 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01978 | hp2 | a0014 | c0016 | t0001 | g0007 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01981 | hp1 | a0019 | c0022 | t0001 | g0113 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01981 | hp2 | a0014 | c0016 | t0001 | g0007 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01993 | hp1 | a0005 | c0005 | t0003 | g0215 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG01993 | hp2 | a0029 | c0045 | t0003 | g0207 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02004 | hp2 | a0030 | c0057 | t0002 | g0015 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02055 | hp1 | a0009 | c0010 | t0001 | g0009 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02055 | hp2 | a0031 | c0056 | t0002 | g0037 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02080 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02135 | hp1 | a0001 | c0017 | t0001 | g0138 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02135 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02145 | hp1 | a0032 | c0035 | t0002 | g0040 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02145 | hp2 | a0004 | c0004 | t0002 | g0025 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02257 | hp1 | a0012 | c0015 | t0004 | g0055 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02257 | hp2 | a0021 | c0028 | t0002 | g0200 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02273 | hp1 | a0008 | c0006 | t0001 | g0112 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0066 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02280 | hp1 | a0006 | c0007 | t0002 | g0048 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02280 | hp2 | a0033 | c0049 | t0004 | g0052 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02451 | hp1 | a0016 | c0029 | t0004 | g0028 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02451 | hp2 | a0022 | c0025 | t0002 | g0204 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02523 | hp1 | a0005 | c0005 | t0003 | g0211 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02523 | hp2 | a0034 | c0036 | t0001 | g0096 | EAS | KHV | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02572 | hp1 | a0004 | c0004 | t0002 | g0198 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02615 | hp1 | a0011 | c0014 | t0002 | g0033 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02615 | hp2 | a0018 | c0019 | t0001 | g0081 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02622 | hp1 | a0008 | c0006 | t0001 | g0017 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02622 | hp2 | a0007 | c0012 | t0001 | g0008 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02630 | hp1 | a0022 | c0025 | t0012 | g0203 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02630 | hp2 | a0013 | c0018 | t0002 | g0205 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02647 | hp2 | a0004 | c0004 | t0002 | g0026 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02698 | hp2 | a0002 | c0002 | t0005 | g0016 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02717 | hp1 | a0004 | c0013 | t0002 | g0042 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02717 | hp2 | a0009 | c0010 | t0001 | g0009 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02723 | hp1 | a0009 | c0010 | t0001 | g0124 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02809 | hp1 | a0007 | c0012 | t0001 | g0008 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02809 | hp2 | a0035 | c0061 | t0004 | g0060 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02886 | hp1 | a0011 | c0014 | t0002 | g0031 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02886 | hp2 | a0018 | c0019 | t0001 | g0083 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02895 | hp1 | a0007 | c0009 | t0001 | g0156 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02895 | hp2 | a0004 | c0004 | t0002 | g0191 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02896 | hp1 | a0004 | c0004 | t0002 | g0024 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02896 | hp2 | a0006 | c0030 | t0002 | g0013 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02897 | hp1 | a0006 | c0030 | t0002 | g0013 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02897 | hp2 | a0004 | c0004 | t0002 | g0190 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02922 | hp1 | a0013 | c0018 | t0002 | g0195 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02922 | hp2 | a0012 | c0015 | t0004 | g0053 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02965 | hp1 | a0004 | c0013 | t0002 | g0043 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02965 | hp2 | a0013 | c0018 | t0002 | g0199 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02970 | hp1 | a0018 | c0019 | t0001 | g0082 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02970 | hp2 | a0004 | c0004 | t0002 | g0197 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02976 | hp1 | a0021 | c0028 | t0002 | g0201 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02976 | hp2 | a0006 | c0007 | t0002 | g0006 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03017 | hp1 | a0023 | c0023 | t0001 | g0086 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03041 | hp2 | a0036 | c0051 | t0001 | g0178 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03098 | hp1 | a0004 | c0013 | t0002 | g0046 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03098 | hp2 | a0007 | c0012 | t0001 | g0087 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03130 | hp1 | a0007 | c0012 | t0001 | g0008 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03130 | hp2 | a0008 | c0006 | t0001 | g0017 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03139 | hp1 | a0037 | c0053 | t0004 | g0059 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03139 | hp2 | a0024 | c0026 | t0002 | g0051 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03195 | hp1 | a0038 | c0058 | t0002 | g0036 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03195 | hp2 | a0015 | c0024 | t0002 | g0014 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03209 | hp1 | a0039 | c0047 | t0002 | g0045 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03209 | hp2 | a0006 | c0007 | t0002 | g0006 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03225 | hp1 | a0004 | c0004 | t0002 | g0202 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03225 | hp2 | a0006 | c0007 | t0002 | g0047 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03239 | hp1 | a0001 | c0042 | t0001 | g0153 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03239 | hp2 | a0017 | c0020 | t0006 | g0188 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03453 | hp1 | a0040 | c0046 | t0002 | g0038 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03453 | hp2 | a0012 | c0015 | t0004 | g0056 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03491 | hp1 | a0003 | c0059 | t0002 | g0072 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03491 | hp2 | a0001 | c0011 | t0001 | g0118 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03492 | hp2 | a0001 | c0011 | t0001 | g0128 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03516 | hp1 | a0041 | c0041 | t0001 | g0177 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03516 | hp2 | a0004 | c0004 | t0002 | g0194 | AFR | ESN | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03540 | hp1 | a0042 | c0062 | t0001 | g0009 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03540 | hp2 | a0024 | c0026 | t0002 | g0035 | AFR | GWD | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03579 | hp1 | a0009 | c0010 | t0001 | g0123 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03579 | hp2 | a0006 | c0007 | t0002 | g0006 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03654 | hp1 | a0001 | c0011 | t0001 | g0010 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03688 | hp1 | a0003 | c0003 | t0013 | g0070 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03704 | hp1 | a0002 | c0002 | t0005 | g0003 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03704 | hp2 | a0043 | c0043 | t0006 | g0212 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03710 | hp2 | a0044 | c0038 | t0001 | g0146 | SAS | PJL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03831 | hp1 | a0005 | c0005 | t0003 | g0213 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03831 | hp2 | a0003 | c0003 | t0002 | g0061 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03834 | hp1 | a0017 | c0020 | t0006 | g0186 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03834 | hp2 | a0002 | c0002 | t0005 | g0016 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03927 | hp1 | a0023 | c0023 | t0001 | g0166 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03927 | hp2 | a0007 | c0009 | t0001 | g0150 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04115 | hp2 | a0001 | c0011 | t0001 | g0010 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04199 | hp2 | a0020 | c0027 | t0001 | g0160 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0067 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18522 | hp1 | a0015 | c0024 | t0002 | g0014 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18612 | hp1 | a0007 | c0009 | t0001 | g0163 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18906 | hp1 | a0046 | c0048 | t0002 | g0025 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18906 | hp2 | a0047 | c0054 | t0002 | g0184 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18941 | hp1 | a0025 | c0021 | t0001 | g0114 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18943 | hp1 | a0005 | c0005 | t0003 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18943 | hp2 | a0010 | c0008 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18950 | hp1 | a0010 | c0008 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18952 | hp1 | a0005 | c0005 | t0003 | g0209 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18952 | hp2 | a0001 | c0001 | t0011 | g0173 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18962 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18964 | hp1 | a0008 | c0006 | t0001 | g0018 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18965 | hp1 | a0008 | c0006 | t0001 | g0085 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18965 | hp2 | a0008 | c0006 | t0001 | g0111 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18969 | hp1 | a0001 | c0017 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18973 | hp2 | a0005 | c0005 | t0003 | g0214 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18982 | hp1 | a0005 | c0005 | t0003 | g0210 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18988 | hp2 | a0025 | c0021 | t0001 | g0167 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18990 | hp1 | a0010 | c0008 | t0001 | g0079 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18994 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18998 | hp1 | a0005 | c0005 | t0003 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18998 | hp2 | a0010 | c0008 | t0001 | g0004 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19011 | hp1 | a0048 | c0037 | t0001 | g0145 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19011 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19012 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19030 | hp2 | a0016 | c0052 | t0001 | g0154 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19043 | hp1 | a0004 | c0004 | t0002 | g0193 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19043 | hp2 | a0004 | c0013 | t0002 | g0044 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19054 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19074 | hp1 | a0005 | c0005 | t0003 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19074 | hp2 | a0001 | c0017 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19082 | hp2 | a0005 | c0005 | t0003 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19091 | hp1 | a0010 | c0008 | t0001 | g0115 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19091 | hp2 | a0005 | c0005 | t0003 | g0005 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19240 | hp1 | a0049 | c0060 | t0004 | g0057 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA19240 | hp2 | a0009 | c0010 | t0001 | g0125 | AFR | YRI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0026 | AFR | ASW | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20752 | hp1 | a0050 | c0040 | t0010 | g0130 | EUR | TSI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20752 | hp2 | a0008 | c0006 | t0001 | g0105 | EUR | TSI | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20905 | hp1 | a0002 | c0002 | t0007 | g0003 | SAS | GIH | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20905 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | GIH | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02109 | hp1 | a0015 | c0055 | t0002 | g0030 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02109 | hp2 | a0006 | c0007 | t0002 | g0006 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02486 | hp1 | a0017 | c0020 | t0006 | g0187 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02486 | hp2 | a0004 | c0004 | t0002 | g0024 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02559 | hp1 | a0011 | c0014 | t0002 | g0032 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG02559 | hp2 | a0004 | c0004 | t0002 | g0185 | AFR | ACB | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03471 | hp1 | a0006 | c0007 | t0002 | g0049 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG03471 | hp2 | a0016 | c0029 | t0004 | g0029 | AFR | MSL | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG06807 | hp1 | a0045 | c0050 | t0004 | g0058 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
HG06807 | hp2 | a0004 | c0004 | t0002 | g0192 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18955 | hp1 | a0008 | c0006 | t0001 | g0018 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA18955 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20300 | hp1 | a0005 | c0005 | t0003 | g0012 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA20300 | hp2 | a0007 | c0009 | t0001 | g0129 | AFR | USA | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA21309 | hp1 | a0004 | c0004 | t0002 | g0196 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0097 | REF | REF | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
homoSapiens | grch38p0 | a0007 | c0009 | t0001 | g0140 | REF | REF | CENPF_chr1_214598195_214669571 | CENPF | chr1 | 214598195 | 214669571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214622111 | C | T | 2 | a0009 a0042 |
6 | HG02055.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.898C>T | p.Arg300Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/20 | 1066/10290 | 898/9345 | 300/3114 | chr1 | 214622111 | |||
chr1:214622268 | A | G | 1 | a0035 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1055A>G | p.Gln352Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/20 | 1223/10290 | 1055/9345 | 352/3114 | chr1 | 214622268 | |||
chr1:214629122 | G | A | 1 | a0022 | 2 | HG02451.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.1145G>A | p.Arg382Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/20 | 1313/10290 | 1145/9345 | 382/3114 | chr1 | 214629122 | |||
chr1:214630582 | A | C | 2 | a0012 a0049 |
5 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.1243A>C | p.Ile415Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1411/10290 | 1243/9345 | 415/3114 | chr1 | 214630582 | |||
chr1:214637901 | C | G | 31 | a0003 a0004 a0005 others(28): Show |
120 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(117): Show |
missense_variant | MODERATE | c.1482C>G | p.His494Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/20 | 1650/10290 | 1482/9345 | 494/3114 | chr1 | 214637901 | |||
chr1:214640043 | T | C | 1 | a0034 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1705T>C | p.Cys569Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 1873/10290 | 1705/9345 | 569/3114 | chr1 | 214640043 | |||
chr1:214640439 | A | C | 2 | a0018 a0047 |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.2101A>C | p.Met701Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2269/10290 | 2101/9345 | 701/3114 | chr1 | 214640439 | |||
chr1:214640439 | A | G | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2101A>G | p.Met701Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2269/10290 | 2101/9345 | 701/3114 | chr1 | 214640439 | |||
chr1:214640598 | C | G | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2260C>G | p.Gln754Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2428/10290 | 2260/9345 | 754/3114 | chr1 | 214640598 | |||
chr1:214640716 | T | G | 4 | a0005 a0026 a0029 others(1): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
missense_variant | MODERATE | c.2378T>G | p.Met793Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2546/10290 | 2378/9345 | 793/3114 | chr1 | 214640716 | |||
chr1:214640782 | G | A | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.2444G>A | p.Arg815His | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2612/10290 | 2444/9345 | 815/3114 | chr1 | 214640782 | |||
chr1:214641390 | T | G | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.3052T>G | p.Tyr1018Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3220/10290 | 3052/9345 | 1018/3114 | chr1 | 214641390 | |||
chr1:214641435 | G | A | 11 | a0003 a0006 a0011 others(8): Show |
56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
missense_variant | MODERATE | c.3097G>A | p.Gly1033Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3265/10290 | 3097/9345 | 1033/3114 | chr1 | 214641435 | |||
chr1:214641451 | A | G | 1 | a0040 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3113A>G | p.Asp1038Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3281/10290 | 3113/9345 | 1038/3114 | chr1 | 214641451 | |||
chr1:214641582 | C | T | 1 | a0017 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.3244C>T | p.His1082Tyr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3412/10290 | 3244/9345 | 1082/3114 | chr1 | 214641582 | |||
chr1:214641652 | C | T | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.3314C>T | p.Thr1105Ile | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3482/10290 | 3314/9345 | 1105/3114 | chr1 | 214641652 | |||
chr1:214641773 | A | T | 4 | a0006 a0011 a0018 others(1): Show |
18 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.3435A>T | p.Glu1145Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3603/10290 | 3435/9345 | 1145/3114 | chr1 | 214641773 | |||
chr1:214641961 | C | T | 2 | a0026 a0029 |
2 | HG01358.hp1 HG01993.hp2 |
missense_variant | MODERATE | c.3623C>T | p.Ala1208Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3791/10290 | 3623/9345 | 1208/3114 | chr1 | 214641961 | |||
chr1:214642266 | C | G | 1 | a0024 | 2 | HG03139.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.3928C>G | p.Leu1310Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4096/10290 | 3928/9345 | 1310/3114 | chr1 | 214642266 | |||
chr1:214642573 | T | C | 7 | a0003 a0015 a0017 others(4): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
missense_variant | MODERATE | c.4235T>C | p.Leu1412Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4403/10290 | 4235/9345 | 1412/3114 | chr1 | 214642573 | |||
chr1:214642627 | C | G | 1 | a0038 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.4289C>G | p.Ser1430Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4457/10290 | 4289/9345 | 1430/3114 | chr1 | 214642627 | |||
chr1:214642881 | G | A | 30 | a0003 a0004 a0005 others(27): Show |
119 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(116): Show |
missense_variant | MODERATE | c.4543G>A | p.Ala1515Thr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4711/10290 | 4543/9345 | 1515/3114 | chr1 | 214642881 | |||
chr1:214642954 | A | G | 2 | a0003 a0030 |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
missense_variant | MODERATE | c.4616A>G | p.Lys1539Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4784/10290 | 4616/9345 | 1539/3114 | chr1 | 214642954 | |||
chr1:214643295 | C | T | 1 | a0030 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.4957C>T | p.Arg1653Trp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 5125/10290 | 4957/9345 | 1653/3114 | chr1 | 214643295 | |||
chr1:214644678 | A | G | 4 | a0006 a0011 a0018 others(1): Show |
18 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.5108A>G | p.Asn1703Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5276/10290 | 5108/9345 | 1703/3114 | chr1 | 214644678 | |||
chr1:214644872 | G | A | 8 | a0003 a0015 a0017 others(5): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.5302G>A | p.Asp1768Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5470/10290 | 5302/9345 | 1768/3114 | chr1 | 214644872 | |||
chr1:214644880 | T | A | 20 | a0003 a0004 a0005 others(17): Show |
101 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(98): Show |
missense_variant | MODERATE | c.5310T>A | p.His1770Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5478/10290 | 5310/9345 | 1770/3114 | chr1 | 214644880 | |||
chr1:214644903 | A | G | 1 | a0046 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.5333A>G | p.Glu1778Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5501/10290 | 5333/9345 | 1778/3114 | chr1 | 214644903 | |||
chr1:214644963 | A | G | 1 | a0041 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.5393A>G | p.Glu1798Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5561/10290 | 5393/9345 | 1798/3114 | chr1 | 214644963 | |||
chr1:214645205 | C | T | 1 | a0017 | 3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.5635C>T | p.Arg1879Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5803/10290 | 5635/9345 | 1879/3114 | chr1 | 214645205 | |||
chr1:214645284 | G | A | 1 | a0033 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.5714G>A | p.Ser1905Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 5882/10290 | 5714/9345 | 1905/3114 | chr1 | 214645284 | |||
chr1:214645461 | G | A | 1 | a0045 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.5891G>A | p.Arg1964His | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6059/10290 | 5891/9345 | 1964/3114 | chr1 | 214645461 | |||
chr1:214645494 | C | T | 2 | a0018 a0047 |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.5924C>T | p.Thr1975Met | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6092/10290 | 5924/9345 | 1975/3114 | chr1 | 214645494 | |||
chr1:214645503 | A | G | 8 | a0003 a0015 a0017 others(5): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.5933A>G | p.Asp1978Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6101/10290 | 5933/9345 | 1978/3114 | chr1 | 214645503 | |||
chr1:214645569 | A | G | 1 | a0037 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.5999A>G | p.His2000Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6167/10290 | 5999/9345 | 2000/3114 | chr1 | 214645569 | |||
chr1:214645602 | A | C | 9 | a0003 a0015 a0017 others(6): Show |
42 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(39): Show |
missense_variant | MODERATE | c.6032A>C | p.Glu2011Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6200/10290 | 6032/9345 | 2011/3114 | chr1 | 214645602 | |||
chr1:214645701 | C | T | 6 | a0015 a0017 a0021 others(3): Show |
12 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
missense_variant | MODERATE | c.6131C>T | p.Ser2044Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6299/10290 | 6131/9345 | 2044/3114 | chr1 | 214645701 | |||
chr1:214645785 | C | A | 1 | a0049 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6215C>A | p.Ser2072Tyr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6383/10290 | 6215/9345 | 2072/3114 | chr1 | 214645785 | |||
chr1:214645985 | G | A | 8 | a0003 a0015 a0017 others(5): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.6415G>A | p.Ala2139Thr | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6583/10290 | 6415/9345 | 2139/3114 | chr1 | 214645985 | |||
chr1:214646003 | C | T | 1 | a0018 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.6433C>T | p.Arg2145Cys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6601/10290 | 6433/9345 | 2145/3114 | chr1 | 214646003 | |||
chr1:214646043 | A | G | 1 | a0023 | 2 | HG03017.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.6473A>G | p.Asn2158Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6641/10290 | 6473/9345 | 2158/3114 | chr1 | 214646043 | |||
chr1:214646173 | T | G | 1 | a0048 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.6603T>G | p.Phe2201Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6771/10290 | 6603/9345 | 2201/3114 | chr1 | 214646173 | |||
chr1:214646244 | A | G | 8 | a0003 a0015 a0017 others(5): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.6674A>G | p.Gln2225Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 6842/10290 | 6674/9345 | 2225/3114 | chr1 | 214646244 | |||
chr1:214646438 | G | A | 1 | a0039 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.6868G>A | p.Asp2290Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7036/10290 | 6868/9345 | 2290/3114 | chr1 | 214646438 | |||
chr1:214646439 | A | T | 1 | a0039 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.6869A>T | p.Asp2290Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7037/10290 | 6869/9345 | 2290/3114 | chr1 | 214646439 | |||
chr1:214646475 | G | A | 1 | a0025 | 2 | NA18941.hp1 NA18988.hp2 |
missense_variant | MODERATE | c.6905G>A | p.Ser2302Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7073/10290 | 6905/9345 | 2302/3114 | chr1 | 214646475 | |||
chr1:214646507 | G | A | 1 | a0028 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.6937G>A | p.Asp2313Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7105/10290 | 6937/9345 | 2313/3114 | chr1 | 214646507 | |||
chr1:214646637 | C | T | 8 | a0003 a0015 a0017 others(5): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.7067C>T | p.Ala2356Val | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7235/10290 | 7067/9345 | 2356/3114 | chr1 | 214646637 | |||
chr1:214646736 | C | G | 1 | a0031 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.7166C>G | p.Thr2389Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7334/10290 | 7166/9345 | 2389/3114 | chr1 | 214646736 | |||
chr1:214646756 | A | G | 7 | a0002 a0008 a0010 others(4): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
missense_variant | MODERATE | c.7186A>G | p.Asn2396Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7354/10290 | 7186/9345 | 2396/3114 | chr1 | 214646756 | |||
chr1:214646896 | G | A | 1 | a0024 | 2 | HG03139.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.7326G>A | p.Met2442Ile | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7494/10290 | 7326/9345 | 2442/3114 | chr1 | 214646896 | |||
chr1:214647125 | A | G | 1 | a0018 | 3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.7555A>G | p.Lys2519Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7723/10290 | 7555/9345 | 2519/3114 | chr1 | 214647125 | |||
chr1:214647227 | G | A | 1 | a0010 | 5 | NA18943.hp2 NA18950.hp1 NA18990.hp1 others(2): Show |
missense_variant | MODERATE | c.7657G>A | p.Glu2553Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7825/10290 | 7657/9345 | 2553/3114 | chr1 | 214647227 | |||
chr1:214647339 | A | T | 1 | a0029 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.7769A>T | p.Tyr2590Phe | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7937/10290 | 7769/9345 | 2590/3114 | chr1 | 214647339 | |||
chr1:214652853 | G | A | 20 | a0001 a0003 a0005 others(17): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
missense_variant | MODERATE | c.8186G>A | p.Arg2729Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/20 | 8354/10290 | 8186/9345 | 2729/3114 | chr1 | 214652853 | |||
chr1:214657274 | A | G | 26 | a0001 a0003 a0005 others(23): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
missense_variant | MODERATE | c.8827A>G | p.Arg2943Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/20 | 8995/10290 | 8827/9345 | 2943/3114 | chr1 | 214657274 | |||
chr1:214663730 | G | A | 1 | a0027 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.9281G>A | p.Arg3094Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9449/10290 | 9281/9345 | 3094/3114 | chr1 | 214663730 | |||
chr1:214663767 | C | G | 29 | a0001 a0003 a0005 others(26): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
missense_variant | MODERATE | c.9318C>G | p.Asn3106Lys | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9486/10290 | 9318/9345 | 3106/3114 | chr1 | 214663767 | |||
chr1:214663768 | G | A | 1 | a0036 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.9319G>A | p.Gly3107Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 9487/10290 | 9319/9345 | 3107/3114 | chr1 | 214663768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214613787 | G | A | 8 | a0002c0002 a0002c0032 a0008c0006 others(5): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
synonymous_variant | LOW | c.33G>A | p.Gly11Gly | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/20 | 201/10290 | 33/9345 | 11/3114 | chr1 | 214613787 | |||
chr1:214619209 | T | C | 1 | a0015c0024 | 2 | HG03195.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.562T>C | p.Leu188Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/20 | 730/10290 | 562/9345 | 188/3114 | chr1 | 214619209 | |||
chr1:214620936 | G | A | 3 | a0004c0033 a0013c0034 a0032c0035 |
3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
synonymous_variant | LOW | c.855G>A | p.Ala285Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/20 | 1023/10290 | 855/9345 | 285/3114 | chr1 | 214620936 | |||
chr1:214630557 | T | G | 1 | a0024c0026 | 2 | HG03139.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1218T>G | p.Ser406Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1386/10290 | 1218/9345 | 406/3114 | chr1 | 214630557 | |||
chr1:214630596 | C | G | 1 | a0024c0026 | 2 | HG03139.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.1257C>G | p.Ala419Ala | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/20 | 1425/10290 | 1257/9345 | 419/3114 | chr1 | 214630596 | |||
chr1:214640144 | A | G | 14 | a0003c0003 a0003c0059 a0006c0007 others(11): Show |
56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
synonymous_variant | LOW | c.1806A>G | p.Leu602Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 1974/10290 | 1806/9345 | 602/3114 | chr1 | 214640144 | |||
chr1:214640352 | A | C | 1 | a0001c0042 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2014A>C | p.Arg672Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 2182/10290 | 2014/9345 | 672/3114 | chr1 | 214640352 | |||
chr1:214641228 | C | T | 8 | a0002c0002 a0002c0032 a0008c0006 others(5): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
synonymous_variant | LOW | c.2890C>T | p.Leu964Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3058/10290 | 2890/9345 | 964/3114 | chr1 | 214641228 | |||
chr1:214641239 | G | A | 9 | a0003c0003 a0003c0059 a0015c0024 others(6): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
synonymous_variant | LOW | c.2901G>A | p.Arg967Arg | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3069/10290 | 2901/9345 | 967/3114 | chr1 | 214641239 | |||
chr1:214641414 | C | T | 1 | a0002c0032 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.3076C>T | p.Leu1026Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3244/10290 | 3076/9345 | 1026/3114 | chr1 | 214641414 | |||
chr1:214641440 | T | C | 1 | a0040c0046 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.3102T>C | p.Asn1034Asn | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3270/10290 | 3102/9345 | 1034/3114 | chr1 | 214641440 | |||
chr1:214641461 | A | G | 1 | a0011c0014 | 4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.3123A>G | p.Gln1041Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3291/10290 | 3123/9345 | 1041/3114 | chr1 | 214641461 | |||
chr1:214641645 | T | C | 1 | a0001c0011 | 4 | HG03491.hp2 HG03492.hp2 HG03654.hp1 others(1): Show |
synonymous_variant | LOW | c.3307T>C | p.Leu1103Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3475/10290 | 3307/9345 | 1103/3114 | chr1 | 214641645 | |||
chr1:214641707 | C | T | 1 | a0003c0059 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.3369C>T | p.Ser1123Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 3537/10290 | 3369/9345 | 1123/3114 | chr1 | 214641707 | |||
chr1:214642289 | C | T | 1 | a0001c0017 | 3 | HG02135.hp1 NA18969.hp1 NA19074.hp2 |
synonymous_variant | LOW | c.3951C>T | p.Leu1317Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4119/10290 | 3951/9345 | 1317/3114 | chr1 | 214642289 | |||
chr1:214642799 | T | G | 9 | a0003c0003 a0003c0059 a0015c0024 others(6): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
synonymous_variant | LOW | c.4461T>G | p.Leu1487Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/20 | 4629/10290 | 4461/9345 | 1487/3114 | chr1 | 214642799 | |||
chr1:214646539 | A | G | 2 | a0004c0013 a0039c0047 |
5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.6969A>G | p.Gln2323Gln | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7137/10290 | 6969/9345 | 2323/3114 | chr1 | 214646539 | |||
chr1:214646956 | A | G | 10 | a0003c0003 a0003c0059 a0015c0024 others(7): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7386A>G | p.Glu2462Glu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7554/10290 | 7386/9345 | 2462/3114 | chr1 | 214646956 | |||
chr1:214647076 | A | G | 2 | a0004c0013 a0039c0047 |
5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.7506A>G | p.Ser2502Ser | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7674/10290 | 7506/9345 | 2502/3114 | chr1 | 214647076 | |||
chr1:214647151 | G | A | 10 | a0003c0003 a0003c0059 a0015c0024 others(7): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7581G>A | p.Leu2527Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7749/10290 | 7581/9345 | 2527/3114 | chr1 | 214647151 | |||
chr1:214647181 | T | C | 10 | a0003c0003 a0003c0059 a0015c0024 others(7): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
synonymous_variant | LOW | c.7611T>C | p.Leu2537Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/20 | 7779/10290 | 7611/9345 | 2537/3114 | chr1 | 214647181 | |||
chr1:214651746 | T | C | 1 | a0006c0030 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.8020T>C | p.Leu2674Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/20 | 8188/10290 | 8020/9345 | 2674/3114 | chr1 | 214651746 | |||
chr1:214655246 | C | T | 7 | a0004c0013 a0004c0033 a0007c0012 others(4): Show |
14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
synonymous_variant | LOW | c.8328C>T | p.Asp2776Asp | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/20 | 8496/10290 | 8328/9345 | 2776/3114 | chr1 | 214655246 | |||
chr1:214658968 | C | T | 3 | a0016c0052 a0031c0056 a0036c0051 |
3 | HG02055.hp2 HG03041.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.9081C>T | p.Leu3027Leu | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/20 | 9249/10290 | 9081/9345 | 3027/3114 | chr1 | 214658968 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214603264 | C | G | 31 | a0002c0002t0002 a0003c0003t0002 a0003c0003t0013 others(28): Show |
107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-99C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/20 | 10491 | chr1 | 214603264 | ||||||
chr1:214603306 | C | G | 7 | a0012c0015t0004 a0016c0029t0004 a0033c0049t0004 others(4): Show |
11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-57C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/20 | 10449 | chr1 | 214603306 | ||||||
chr1:214663867 | T | C | 1 | a0002c0002t0005 | 4 | HG00639.hp2 HG02698.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*73T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 73 | chr1 | 214663867 | ||||||
chr1:214663910 | C | T | 1 | a0001c0001t0011 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 116 | chr1 | 214663910 | ||||||
chr1:214663928 | A | G | 1 | a0013c0034t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 134 | chr1 | 214663928 | ||||||
chr1:214663956 | G | C | 1 | a0022c0025t0012 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 162 | chr1 | 214663956 | ||||||
chr1:214663993 | G | A | 5 | a0001c0001t0008 a0003c0003t0013 a0005c0005t0003 others(2): Show |
19 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 199 | chr1 | 214663993 | ||||||
chr1:214664326 | C | T | 3 | a0017c0020t0006 a0043c0043t0006 a0050c0040t0010 |
5 | HG02486.hp1 HG03239.hp2 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*532C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 532 | chr1 | 214664326 | ||||||
chr1:214664331 | A | G | 1 | a0013c0034t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 537 | chr1 | 214664331 | ||||||
chr1:214664380 | G | A | 1 | a0002c0002t0007 | 2 | HG01433.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 586 | chr1 | 214664380 | ||||||
chr1:214664441 | G | A | 1 | a0003c0003t0013 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 647 | chr1 | 214664441 | ||||||
chr1:214664547 | A | G | 1 | a0001c0001t0009 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 20/20 | 753 | chr1 | 214664547 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:214603487 | C | G | 40 | a0002c0002t0002g0027 a0002c0002t0002g0208 a0004c0004t0002g0024 others(37): Show |
49 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-42+166C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603487 | |||||||
chr1:214603537 | T | C | 95 | a0002c0002t0002g0027 a0002c0002t0002g0208 a0003c0003t0002g0002 others(92): Show |
118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-42+216T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603537 | |||||||
chr1:214603585 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-42+264C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603585 | |||||||
chr1:214603593 | G | A | 26 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+272G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603593 | |||||||
chr1:214603752 | T | C | 26 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+431T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603752 | |||||||
chr1:214603823 | AT | A | 34 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0004c0013t0002g0042 others(31): Show |
39 | HG00642.hp2 HG01106.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-42+513delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214603823 | ||||||
chr1:214603823 | ATT | A | 39 | a0002c0002t0002g0027 a0002c0002t0002g0208 a0004c0004t0002g0024 others(36): Show |
48 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.-42+512_-42+513del others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214603823 | ||||||
chr1:214603933 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-42+612G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603933 | |||||||
chr1:214603972 | A | G | 1 | a0024c0026t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-42+651A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214603972 | |||||||
chr1:214604073 | G | T | 3 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0018c0019t0001g0083 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-42+752G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604073 | |||||||
chr1:214604311 | T | C | 14 | a0002c0002t0002g0027 a0002c0002t0002g0208 a0005c0005t0003g0005 others(11): Show |
21 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42+990T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604311 | |||||||
chr1:214604466 | T | A | 1 | a0008c0006t0001g0085 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-42+1145T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604466 | |||||||
chr1:214604467 | C | G | 1 | a0002c0002t0001g0183 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-42+1146C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604467 | |||||||
chr1:214604602 | T | G | 2 | a0026c0044t0003g0206 a0029c0045t0003g0207 |
2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-42+1281T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604602 | |||||||
chr1:214604634 | T | C | 26 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+1313T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604634 | |||||||
chr1:214604816 | A | T | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+1495A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604816 | |||||||
chr1:214604864 | G | A | 11 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42+1543G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214604864 | |||||||
chr1:214605066 | C | G | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+1745C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605066 | |||||||
chr1:214605101 | T | A | 36 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(33): Show |
50 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42+1780T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605101 | |||||||
chr1:214605441 | G | GT | 20 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0063 others(17): Show |
29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42+2135dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605441 | ||||||
chr1:214605441 | GT | G | 9 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01070.hp2 HG01496.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42+2135delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605441 | ||||||
chr1:214605455 | T | C | 1 | a0047c0054t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42+2134T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605455 | |||||||
chr1:214605457 | A | T | 2 | a0002c0002t0001g0182 a0015c0024t0002g0014 |
3 | HG00558.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+2136A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605457 | |||||||
chr1:214605481 | T | G | 1 | a0004c0004t0002g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-42+2160T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605481 | |||||||
chr1:214605567 | G | A | 19 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(16): Show |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-42+2246G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605567 | |||||||
chr1:214605585 | CG | C | 26 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+2269delG | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214605585 | ||||||
chr1:214605688 | C | A | 19 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(16): Show |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-42+2367C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605688 | |||||||
chr1:214605804 | T | C | 40 | a0002c0002t0002g0027 a0002c0002t0002g0208 a0004c0004t0002g0024 others(37): Show |
49 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.-42+2483T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605804 | |||||||
chr1:214605809 | G | C | 1 | a0033c0049t0004g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-42+2488G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605809 | |||||||
chr1:214605865 | G | A | 1 | a0002c0002t0001g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-42+2544G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605865 | |||||||
chr1:214605897 | A | G | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-42+2576A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605897 | |||||||
chr1:214605988 | C | T | 26 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+2667C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214605988 | |||||||
chr1:214606004 | C | T | 24 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(21): Show |
33 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-42+2683C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606004 | |||||||
chr1:214606018 | C | T | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2697C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606018 | |||||||
chr1:214606084 | A | C | 37 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(34): Show |
45 | HG01109.hp1 HG01346.hp2 HG01358.hp1 others(42): Show |
intron_variant | MODIFIER | c.-42+2763A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606084 | |||||||
chr1:214606097 | G | A | 7 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(4): Show |
12 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-42+2776G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606097 | |||||||
chr1:214606097 | G | T | 1 | a0018c0019t0001g0083 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-42+2776G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606097 | |||||||
chr1:214606109 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-42+2788G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606109 | |||||||
chr1:214606133 | C | G | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2812C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606133 | |||||||
chr1:214606145 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-42+2824G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606145 | |||||||
chr1:214606273 | C | T | 1 | a0004c0004t0002g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-42+2952C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606273 | |||||||
chr1:214606276 | G | T | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+2955G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606276 | |||||||
chr1:214606283 | C | T | 1 | a0002c0002t0001g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-42+2962C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606283 | |||||||
chr1:214606286 | CCCGTTCC others(9): Show |
C | 38 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(35): Show |
53 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.-42+2979_-42+2994d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214606286 | ||||||
chr1:214606314 | C | T | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-42+2993C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606314 | |||||||
chr1:214606371 | T | A | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+3050T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606371 | |||||||
chr1:214606444 | T | G | 1 | a0002c0002t0001g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-42+3123T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606444 | |||||||
chr1:214606467 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-42+3146C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606467 | |||||||
chr1:214606665 | C | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+3344C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606665 | |||||||
chr1:214606718 | C | T | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42+3397C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606718 | |||||||
chr1:214606832 | G | A | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+3511G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606832 | |||||||
chr1:214606985 | C | T | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-42+3664C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214606985 | |||||||
chr1:214607018 | A | T | 1 | a0003c0003t0002g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-42+3697A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607018 | |||||||
chr1:214607050 | G | A | 1 | a0005c0005t0003g0209 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-42+3729G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607050 | |||||||
chr1:214607178 | C | G | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-42+3857C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607178 | |||||||
chr1:214607409 | C | T | 1 | a0036c0051t0001g0178 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-42+4088C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607409 | |||||||
chr1:214607410 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-42+4089G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607410 | |||||||
chr1:214607593 | G | A | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+4272G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607593 | |||||||
chr1:214607844 | G | A | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+4523G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607844 | |||||||
chr1:214607921 | G | A | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+4600G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214607921 | |||||||
chr1:214608100 | G | T | 28 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(25): Show |
30 | HG00642.hp2 HG01109.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-42+4779G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608100 | |||||||
chr1:214608172 | G | C | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42+4851G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608172 | |||||||
chr1:214608231 | C | G | 3 | a0017c0020t0006g0186 a0017c0020t0006g0187 a0017c0020t0006g0188 |
3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-42+4910C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608231 | |||||||
chr1:214608283 | C | T | 1 | a0041c0041t0001g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-42+4962C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608283 | |||||||
chr1:214608342 | C | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+5021C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608342 | |||||||
chr1:214608446 | A | G | 2 | a0021c0028t0002g0200 a0021c0028t0002g0201 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-42+5125A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608446 | |||||||
chr1:214608599 | C | T | 1 | a0024c0026t0002g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-41-5115C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608599 | |||||||
chr1:214608621 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-41-5093C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608621 | |||||||
chr1:214608628 | C | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41-5086C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608628 | |||||||
chr1:214608786 | G | A | 50 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(47): Show |
61 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-41-4928G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608786 | |||||||
chr1:214608810 | A | G | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-4904A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608810 | |||||||
chr1:214608944 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-41-4770G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608944 | |||||||
chr1:214608985 | C | T | 2 | a0031c0056t0002g0037 a0040c0046t0002g0038 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-41-4729C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214608985 | |||||||
chr1:214609028 | G | T | 1 | a0028c0031t0001g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-41-4686G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609028 | |||||||
chr1:214609097 | T | C | 92 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(89): Show |
114 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.-41-4617T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609097 | |||||||
chr1:214609122 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-41-4592C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609122 | |||||||
chr1:214609186 | A | AC | 6 | a0001c0001t0001g0176 a0003c0003t0002g0015 a0003c0003t0002g0063 others(3): Show |
6 | HG00544.hp2 HG02004.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-4526dupC | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214609186 | ||||||
chr1:214609563 | C | T | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-4151C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609563 | |||||||
chr1:214609564 | C | T | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-4150C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609564 | |||||||
chr1:214609646 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-4068A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609646 | |||||||
chr1:214609656 | G | T | 14 | a0004c0004t0002g0025 a0004c0004t0002g0026 a0004c0004t0002g0193 others(11): Show |
15 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41-4058G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609656 | |||||||
chr1:214609842 | C | G | 19 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(16): Show |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-41-3872C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609842 | |||||||
chr1:214609991 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-3723T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214609991 | |||||||
chr1:214610019 | C | CT | 9 | a0001c0001t0001g0023 a0001c0001t0001g0090 a0001c0001t0001g0169 others(6): Show |
9 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41-3677dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | ||||||
chr1:214610019 | CT | C | 70 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0084 others(67): Show |
89 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-41-3677delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | ||||||
chr1:214610019 | CTT | C | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41-3678_-41-3677d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610019 | ||||||
chr1:214610119 | A | G | 1 | a0003c0003t0002g0075 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-41-3595A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610119 | |||||||
chr1:214610208 | C | A | 3 | a0004c0033t0002g0039 a0013c0034t0014g0041 a0032c0035t0002g0040 |
3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-41-3506C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610208 | |||||||
chr1:214610441 | A | T | 3 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0018c0019t0001g0083 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-41-3273A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610441 | |||||||
chr1:214610479 | AT | A | 48 | a0001c0011t0001g0118 a0003c0003t0002g0002 a0003c0003t0002g0015 others(45): Show |
58 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-41-3219delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 214610479 | ||||||
chr1:214610484 | T | G | 21 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(18): Show |
23 | HG01109.hp1 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41-3230T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610484 | |||||||
chr1:214610523 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-3191T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610523 | |||||||
chr1:214610551 | G | A | 3 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0018c0019t0001g0083 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-41-3163G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610551 | |||||||
chr1:214610751 | A | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-2963A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610751 | |||||||
chr1:214610771 | G | A | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-41-2943G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610771 | |||||||
chr1:214610838 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-41-2876T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610838 | |||||||
chr1:214610848 | A | G | 21 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(18): Show |
30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.-41-2866A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610848 | |||||||
chr1:214610919 | A | T | 3 | a0017c0020t0006g0186 a0017c0020t0006g0187 a0017c0020t0006g0188 |
3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-41-2795A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214610919 | |||||||
chr1:214611022 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-41-2692A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611022 | |||||||
chr1:214611137 | TG | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41-2576delG | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611137 | |||||||
chr1:214611580 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-41-2134G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611580 | |||||||
chr1:214611678 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-2036T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611678 | |||||||
chr1:214611889 | A | G | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-1825A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611889 | |||||||
chr1:214611893 | G | T | 11 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41-1821G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611893 | |||||||
chr1:214611955 | A | G | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-1759A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214611955 | |||||||
chr1:214612117 | A | G | 1 | a0005c0005t0003g0209 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-41-1597A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612117 | |||||||
chr1:214612300 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-41-1414C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612300 | |||||||
chr1:214612592 | C | T | 1 | a0039c0047t0002g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-41-1122C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612592 | |||||||
chr1:214612691 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-41-1023C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214612691 | |||||||
chr1:214613094 | T | C | 96 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(93): Show |
118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-41-620T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613094 | |||||||
chr1:214613292 | A | C | 140 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(137): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.-41-422A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613292 | |||||||
chr1:214613318 | T | C | 96 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(93): Show |
118 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(115): Show |
intron_variant | MODIFIER | c.-41-396T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613318 | |||||||
chr1:214613402 | C | A | 2 | a0007c0012t0001g0008 a0007c0012t0001g0087 |
4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-312C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613402 | |||||||
chr1:214613457 | T | C | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41-257T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613457 | |||||||
chr1:214613639 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-41-75A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 1/19 | chr1 | 214613639 | |||||||
chr1:214613971 | G | C | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162+55G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214613971 | |||||||
chr1:214614087 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.162+171A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614087 | |||||||
chr1:214614108 | C | CT | 54 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(51): Show |
66 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.162+205dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 214614108 | ||||||
chr1:214614108 | C | CTT | 15 | a0004c0004t0002g0192 a0004c0013t0002g0042 a0004c0013t0002g0043 others(12): Show |
15 | HG00642.hp2 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.162+204_162+205dup others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 214614108 | ||||||
chr1:214614184 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.162+268G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614184 | |||||||
chr1:214614200 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.162+284A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614200 | |||||||
chr1:214614216 | A | G | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+300A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614216 | |||||||
chr1:214614217 | C | T | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162+301C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614217 | |||||||
chr1:214614591 | A | T | 1 | a0018c0019t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.163-241A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 2/19 | chr1 | 214614591 | |||||||
chr1:214615084 | C | T | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.359+56C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615084 | |||||||
chr1:214615121 | T | C | 1 | a0018c0019t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359+93T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615121 | |||||||
chr1:214615157 | C | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(5): Show |
8 | HG00544.hp2 HG02040.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.359+129C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615157 | |||||||
chr1:214615240 | C | T | 3 | a0004c0033t0002g0039 a0013c0034t0014g0041 a0032c0035t0002g0040 |
3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.359+212C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615240 | |||||||
chr1:214615336 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.359+308A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615336 | |||||||
chr1:214615341 | T | G | 1 | a0047c0054t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+313T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615341 | |||||||
chr1:214615389 | T | G | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.359+361T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615389 | |||||||
chr1:214615496 | G | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0168 a0020c0027t0001g0121 others(1): Show |
4 | HG01081.hp2 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+468G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615496 | |||||||
chr1:214615696 | T | C | 1 | a0047c0054t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+668T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615696 | |||||||
chr1:214615994 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.359+966C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615994 | |||||||
chr1:214615997 | A | G | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.359+969A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214615997 | |||||||
chr1:214616032 | T | C | 93 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(90): Show |
115 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.359+1004T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616032 | |||||||
chr1:214616058 | C | T | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.359+1030C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616058 | |||||||
chr1:214616189 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.359+1161T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616189 | |||||||
chr1:214616294 | A | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.359+1266A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616294 | |||||||
chr1:214616561 | A | G | 32 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(29): Show |
34 | HG00642.hp2 HG01106.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.359+1533A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616561 | |||||||
chr1:214616819 | CTTCTTTC others(25): Show |
C | 1 | a0049c0060t0004g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.360-1752_360-1721d others(34): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | ||||||
chr1:214616819 | CTTCTTTC others(33): Show |
C | 1 | a0012c0015t0004g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.360-1752_360-1713d others(42): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | ||||||
chr1:214616819 | CTTCTTTC others(37): Show |
C | 2 | a0012c0015t0004g0054 a0012c0015t0004g0055 |
2 | HG01109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.360-1752_360-1709d others(46): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | ||||||
chr1:214616819 | CTTCTTTC others(41): Show |
C | 1 | a0012c0015t0004g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.360-1752_360-1705d others(50): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616819 | ||||||
chr1:214616827 | CTTCCTTC others(12): Show |
C | 1 | a0032c0035t0002g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.360-1742_360-1724d others(21): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616827 | ||||||
chr1:214616831 | CTTCCTCT others(16): Show |
C | 1 | a0011c0014t0002g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.360-1738_360-1716d others(25): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616831 | ||||||
chr1:214616834 | CCTCTTTC others(1): Show |
C | 3 | a0004c0013t0002g0046 a0011c0014t0002g0031 a0011c0014t0002g0034 |
3 | HG01106.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.360-1738_360-1731d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | |||||||
chr1:214616834 | CCTCTTTC others(5): Show |
C | 2 | a0004c0033t0002g0039 a0013c0034t0014g0041 |
2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.360-1738_360-1727d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | |||||||
chr1:214616834 | CCTCTTTC others(9): Show |
C | 1 | a0004c0013t0002g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360-1738_360-1723d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | |||||||
chr1:214616834 | CCTCTTTC others(13): Show |
C | 4 | a0004c0013t0002g0043 a0004c0013t0002g0044 a0011c0014t0002g0032 others(1): Show |
4 | HG02559.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.360-1738_360-1719d others(22): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616834 | |||||||
chr1:214616834 | CCTCTTTC others(15): Show |
C | 1 | a0017c0020t0006g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360-1736_360-1715d others(24): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616834 | ||||||
chr1:214616835 | C | CTCTTTCT others(5): Show |
1 | a0020c0027t0001g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.360-1661_360-1650d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | C | CTCTTTCT others(9): Show |
1 | a0001c0017t0001g0138 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.360-1665_360-1650d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTT | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0094 others(9): Show |
14 | HG00673.hp2 HG01258.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.360-1653_360-1650d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(1): Show |
C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0088 others(16): Show |
20 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-1657_360-1650d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(5): Show |
C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(32): Show |
42 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.360-1661_360-1650d others(14): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(8): Show |
C | 1 | a0002c0002t0002g0027 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.360-1736_360-1722d others(17): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(9): Show |
C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0023 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.360-1665_360-1650d others(18): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(13): Show |
C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(32): Show |
37 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.360-1669_360-1650d others(22): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(17): Show |
C | 30 | a0001c0001t0001g0090 a0001c0001t0001g0134 a0001c0001t0001g0144 others(27): Show |
33 | HG00140.hp2 HG01074.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.360-1673_360-1650d others(26): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(21): Show |
C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0119 others(19): Show |
25 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.360-1677_360-1650d others(30): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(25): Show |
C | 6 | a0002c0002t0001g0182 a0003c0003t0002g0002 a0005c0005t0003g0213 others(3): Show |
8 | HG00558.hp2 HG02622.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.360-1681_360-1650d others(34): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(29): Show |
C | 3 | a0003c0003t0002g0073 a0005c0005t0003g0012 a0005c0005t0003g0216 |
3 | HG00408.hp2 HG01346.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.360-1685_360-1650d others(38): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(33): Show |
C | 4 | a0005c0005t0003g0005 a0005c0005t0003g0210 a0005c0005t0003g0214 others(1): Show |
8 | HG03704.hp2 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.360-1689_360-1650d others(42): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616835 | CTCTTTCT others(37): Show |
C | 1 | a0005c0005t0003g0012 | 2 | HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.360-1693_360-1650d others(46): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616835 | ||||||
chr1:214616841 | CTTTCTTT others(10): Show |
C | 1 | a0002c0002t0005g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.360-1729_360-1713d others(19): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616841 | ||||||
chr1:214616850 | T | C | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-1723T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616850 | |||||||
chr1:214616858 | T | C | 1 | a0017c0020t0006g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.360-1715T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616858 | |||||||
chr1:214616862 | TTTCTTTC others(12): Show |
T | 1 | a0014c0016t0001g0007 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.360-1708_360-1690d others(21): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616862 | ||||||
chr1:214616873 | C | A | 2 | a0016c0029t0004g0029 a0033c0049t0004g0052 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.360-1700C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616873 | |||||||
chr1:214616877 | C | A | 1 | a0016c0029t0004g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.360-1696C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616877 | |||||||
chr1:214616888 | TCTTTCTT others(44): Show |
T | 1 | a0004c0004t0002g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.360-1683_360-1633d others(53): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616888 | ||||||
chr1:214616892 | TCTTTCTT others(40): Show |
T | 1 | a0004c0004t0002g0192 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.360-1679_360-1633d others(49): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616892 | ||||||
chr1:214616893 | CT | C | 4 | a0004c0004t0002g0190 a0004c0004t0002g0191 a0004c0004t0002g0193 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1677delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616893 | ||||||
chr1:214616896 | TCTTTCTT others(36): Show |
T | 2 | a0021c0028t0002g0200 a0021c0028t0002g0201 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.360-1675_360-1633d others(45): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616896 | ||||||
chr1:214616900 | TCTTTCTT others(32): Show |
T | 1 | a0004c0004t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.360-1671_360-1633d others(41): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616900 | ||||||
chr1:214616904 | TCTTTCTT others(28): Show |
T | 4 | a0004c0004t0002g0190 a0004c0004t0002g0191 a0004c0004t0002g0193 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1667_360-1633d others(37): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616904 | ||||||
chr1:214616905 | CTTTCTTT others(6): Show |
C | 1 | a0004c0004t0002g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.360-1665_360-1653d others(15): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616905 | ||||||
chr1:214616918 | TTTC | T | 5 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(2): Show |
5 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-1649_360-1647d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616918 | ||||||
chr1:214616934 | ACCCTCCC others(1): Show |
A | 11 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(8): Show |
13 | HG02145.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.360-1630_360-1623d others(10): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214616934 | ||||||
chr1:214616942 | T | A | 9 | a0004c0004t0002g0189 a0004c0004t0002g0190 a0004c0004t0002g0191 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.360-1631T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616942 | |||||||
chr1:214616964 | C | T | 2 | a0026c0044t0003g0206 a0029c0045t0003g0207 |
2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.360-1609C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214616964 | |||||||
chr1:214617000 | C | CTCTT | 6 | a0002c0002t0001g0117 a0004c0013t0002g0043 a0004c0013t0002g0044 others(3): Show |
6 | HG02109.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.360-1557_360-1554d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr1 | 214617000 | ||||||
chr1:214617291 | G | A | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.360-1282G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617291 | |||||||
chr1:214617345 | G | A | 1 | a0017c0020t0006g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.360-1228G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617345 | |||||||
chr1:214617363 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0181 a0034c0036t0001g0096 |
3 | HG02523.hp2 NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.360-1210C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617363 | |||||||
chr1:214617453 | G | A | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.360-1120G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617453 | |||||||
chr1:214617713 | C | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.360-860C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617713 | |||||||
chr1:214617733 | A | G | 1 | a0022c0025t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.360-840A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617733 | |||||||
chr1:214617782 | A | G | 1 | a0004c0004t0002g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.360-791A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617782 | |||||||
chr1:214617798 | C | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.360-775C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617798 | |||||||
chr1:214617949 | T | C | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.360-624T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214617949 | |||||||
chr1:214618093 | C | T | 1 | a0020c0027t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.360-480C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618093 | |||||||
chr1:214618146 | C | T | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-427C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618146 | |||||||
chr1:214618190 | C | T | 2 | a0017c0020t0006g0186 a0017c0020t0006g0188 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.360-383C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618190 | |||||||
chr1:214618269 | C | G | 11 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-304C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618269 | |||||||
chr1:214618441 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.360-132A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618441 | |||||||
chr1:214618511 | A | G | 1 | a0004c0013t0002g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.360-62A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618511 | |||||||
chr1:214618552 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.360-21T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 3/19 | chr1 | 214618552 | |||||||
chr1:214618906 | G | T | 19 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(16): Show |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.481+212G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214618906 | |||||||
chr1:214618937 | A | G | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.482-192A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214618937 | |||||||
chr1:214619006 | C | G | 20 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(17): Show |
29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.482-123C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 4/19 | chr1 | 214619006 | |||||||
chr1:214619260 | T | C | 1 | a0009c0010t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.573+40T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619260 | |||||||
chr1:214619330 | G | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.573+110G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619330 | |||||||
chr1:214619422 | A | G | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+202A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619422 | |||||||
chr1:214619483 | A | G | 1 | a0047c0054t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.573+263A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619483 | |||||||
chr1:214619535 | C | T | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+315C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214619535 | |||||||
chr1:214620040 | T | G | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-615T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620040 | |||||||
chr1:214620043 | C | CAAA | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-606_574-604dup others(3): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 214620043 | ||||||
chr1:214620302 | C | T | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.574-353C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620302 | |||||||
chr1:214620470 | G | A | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.574-185G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620470 | |||||||
chr1:214620513 | A | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.574-142A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620513 | |||||||
chr1:214620525 | G | A | 5 | a0009c0010t0001g0009 a0009c0010t0001g0123 a0009c0010t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-130G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 5/19 | chr1 | 214620525 | |||||||
chr1:214621054 | A | G | 1 | a0004c0013t0002g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.865+108A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621054 | |||||||
chr1:214621153 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.865+207A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621153 | |||||||
chr1:214621183 | C | G | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.865+237C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621183 | |||||||
chr1:214621213 | T | A | 41 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(38): Show |
55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.865+267T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621213 | |||||||
chr1:214621219 | G | A | 1 | a0035c0061t0004g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.865+273G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621219 | |||||||
chr1:214621252 | G | A | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.865+306G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621252 | |||||||
chr1:214621284 | A | C | 1 | a0002c0002t0001g0116 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.865+338A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621284 | |||||||
chr1:214621368 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.865+422A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621368 | |||||||
chr1:214621464 | G | A | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.865+518G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621464 | |||||||
chr1:214621897 | T | C | 1 | a0003c0003t0002g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.866-182T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621897 | |||||||
chr1:214621964 | G | T | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-115G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214621964 | |||||||
chr1:214622040 | A | G | 1 | a0009c0010t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.866-39A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 6/19 | chr1 | 214622040 | |||||||
chr1:214622296 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1068+15G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622296 | |||||||
chr1:214622451 | C | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+170C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622451 | |||||||
chr1:214622492 | T | C | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+211T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622492 | |||||||
chr1:214622556 | T | C | 41 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(38): Show |
55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1068+275T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622556 | |||||||
chr1:214622654 | GGATCGTA others(83): Show |
G | 87 | a0001c0001t0001g0158 a0003c0003t0002g0002 a0003c0003t0002g0015 others(84): Show |
107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.1068+553_1068+642d others(92): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214622654 | ||||||
chr1:214622654 | GGATCGTA others(173): Show |
G | 12 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(9): Show |
16 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1068+463_1068+642d others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214622654 | ||||||
chr1:214622749 | G | A | 1 | a0017c0020t0006g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1068+468G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622749 | |||||||
chr1:214622852 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0098 |
2 | HG00140.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1068+571G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622852 | |||||||
chr1:214622868 | A | G | 3 | a0017c0020t0006g0186 a0017c0020t0006g0187 a0017c0020t0006g0188 |
3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1068+587A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622868 | |||||||
chr1:214622883 | G | C | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+602G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622883 | |||||||
chr1:214622902 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1068+621C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622902 | |||||||
chr1:214622917 | G | A | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+636G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622917 | |||||||
chr1:214622934 | G | A | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+653G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622934 | |||||||
chr1:214622941 | T | C | 41 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(38): Show |
55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1068+660T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622941 | |||||||
chr1:214622963 | A | G | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+682A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622963 | |||||||
chr1:214622967 | T | G | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068+686T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622967 | |||||||
chr1:214622979 | A | G | 1 | a0013c0034t0014g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1068+698A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622979 | |||||||
chr1:214622986 | C | T | 1 | a0007c0009t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1068+705C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214622986 | |||||||
chr1:214623054 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0127 |
2 | HG01978.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1068+773T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623054 | |||||||
chr1:214623056 | C | T | 1 | a0004c0013t0002g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1068+775C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623056 | |||||||
chr1:214623103 | C | T | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1068+822C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623103 | |||||||
chr1:214623147 | G | T | 1 | a0003c0003t0002g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1068+866G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623147 | |||||||
chr1:214623170 | C | G | 1 | a0005c0005t0003g0215 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1068+889C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623170 | |||||||
chr1:214623189 | T | C | 178 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(175): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1068+908T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623189 | |||||||
chr1:214623285 | A | G | 2 | a0005c0005t0003g0012 a0005c0005t0003g0216 |
4 | HG01346.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068+1004A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623285 | |||||||
chr1:214623495 | C | T | 8 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(5): Show |
9 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+1214C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623495 | |||||||
chr1:214623544 | TTTG | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+1281_1068+128 others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214623544 | ||||||
chr1:214623617 | T | G | 19 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(16): Show |
28 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1068+1336T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623617 | |||||||
chr1:214623681 | A | G | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+1400A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623681 | |||||||
chr1:214623713 | G | A | 1 | a0011c0014t0002g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1068+1432G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623713 | |||||||
chr1:214623841 | A | G | 6 | a0002c0002t0001g0004 a0010c0008t0001g0004 a0010c0008t0001g0079 others(3): Show |
9 | NA18941.hp1 NA18943.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1068+1560A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214623841 | |||||||
chr1:214624002 | A | C | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+1721A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624002 | |||||||
chr1:214624010 | ATTTTAAG others(19): Show |
A | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068+1730_1068+175 others(30): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624010 | |||||||
chr1:214624169 | A | AT | 13 | a0004c0004t0002g0194 a0005c0005t0003g0005 a0005c0005t0003g0012 others(10): Show |
19 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1068+1897dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214624169 | ||||||
chr1:214624242 | T | C | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1068+1961T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624242 | |||||||
chr1:214624249 | C | A | 1 | a0002c0002t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1068+1968C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624249 | |||||||
chr1:214624365 | A | G | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1068+2084A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624365 | |||||||
chr1:214624370 | A | C | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1068+2089A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624370 | |||||||
chr1:214624434 | C | G | 1 | a0003c0003t0002g0073 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1068+2153C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624434 | |||||||
chr1:214624531 | T | C | 1 | a0004c0033t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1068+2250T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624531 | |||||||
chr1:214624588 | T | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+2307T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624588 | |||||||
chr1:214624715 | AT | A | 7 | a0001c0011t0001g0118 a0001c0011t0001g0128 a0003c0003t0002g0066 others(4): Show |
8 | HG02273.hp2 HG03139.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+2445delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214624715 | ||||||
chr1:214624776 | C | T | 1 | a0041c0041t0001g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1068+2495C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624776 | |||||||
chr1:214624823 | G | A | 1 | a0001c0017t0001g0138 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1068+2542G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624823 | |||||||
chr1:214624879 | G | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1068+2598G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624879 | |||||||
chr1:214624910 | C | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1068+2629C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624910 | |||||||
chr1:214624978 | A | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+2697A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214624978 | |||||||
chr1:214625143 | A | G | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+2862A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625143 | |||||||
chr1:214625189 | G | C | 1 | a0020c0027t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1068+2908G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625189 | |||||||
chr1:214625237 | C | T | 44 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(41): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1068+2956C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625237 | |||||||
chr1:214625334 | C | A | 10 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(7): Show |
14 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1068+3053C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625334 | |||||||
chr1:214625459 | A | G | 142 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(139): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1068+3178A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625459 | |||||||
chr1:214625493 | T | G | 1 | a0024c0026t0002g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1068+3212T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625493 | |||||||
chr1:214625511 | G | A | 2 | a0016c0029t0004g0028 a0016c0029t0004g0029 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1068+3230G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625511 | |||||||
chr1:214625512 | C | T | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+3231C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625512 | |||||||
chr1:214625551 | A | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1068+3270A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625551 | |||||||
chr1:214625586 | G | C | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1068+3305G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625586 | |||||||
chr1:214625650 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1068+3369T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625650 | |||||||
chr1:214625677 | T | G | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1069-3369T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625677 | |||||||
chr1:214625688 | T | A | 1 | a0002c0002t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1069-3358T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625688 | |||||||
chr1:214625901 | T | C | 2 | a0012c0015t0004g0053 a0012c0015t0004g0054 |
2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1069-3145T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625901 | |||||||
chr1:214625963 | A | G | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-3083A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625963 | |||||||
chr1:214625995 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-3051A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214625995 | |||||||
chr1:214626027 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1069-3019A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626027 | |||||||
chr1:214626035 | A | C | 5 | a0016c0029t0004g0028 a0016c0029t0004g0029 a0033c0049t0004g0052 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-3011A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626035 | |||||||
chr1:214626156 | G | C | 1 | a0006c0007t0002g0050 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1069-2890G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626156 | |||||||
chr1:214626427 | T | A | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1069-2619T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626427 | |||||||
chr1:214626551 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-2495C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626551 | |||||||
chr1:214626785 | C | T | 4 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0049 others(1): Show |
8 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-2261C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626785 | |||||||
chr1:214626804 | T | C | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-2242T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626804 | |||||||
chr1:214626854 | G | A | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069-2192G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626854 | |||||||
chr1:214626864 | T | C | 1 | a0002c0002t0001g0102 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1069-2182T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626864 | |||||||
chr1:214626921 | A | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-2125A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214626921 | |||||||
chr1:214627045 | T | C | 24 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(21): Show |
33 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1069-2001T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627045 | |||||||
chr1:214627129 | A | T | 140 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(137): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1069-1917A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627129 | |||||||
chr1:214627203 | G | A | 1 | a0002c0002t0007g0103 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1069-1843G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627203 | |||||||
chr1:214627204 | C | T | 2 | a0013c0018t0002g0199 a0013c0018t0002g0205 |
2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1069-1842C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627204 | |||||||
chr1:214627250 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1796A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627250 | |||||||
chr1:214627257 | C | T | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1069-1789C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627257 | |||||||
chr1:214627261 | G | A | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-1785G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627261 | |||||||
chr1:214627289 | G | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1757G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627289 | |||||||
chr1:214627369 | C | CT | 122 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(119): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1069-1656dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | ||||||
chr1:214627369 | C | CTT | 44 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0003c0003t0002g0076 others(41): Show |
52 | HG00642.hp2 HG01109.hp1 HG01346.hp2 others(49): Show |
intron_variant | MODIFIER | c.1069-1657_1069-165 others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | ||||||
chr1:214627369 | C | CTTT | 6 | a0004c0013t0002g0046 a0005c0005t0003g0214 a0015c0024t0002g0014 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-1658_1069-165 others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 214627369 | ||||||
chr1:214627476 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-1570T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627476 | |||||||
chr1:214627619 | G | A | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-1427G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627619 | |||||||
chr1:214627806 | C | G | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-1240C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627806 | |||||||
chr1:214627811 | G | A | 2 | a0006c0007t0002g0048 a0006c0007t0002g0050 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1069-1235G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627811 | |||||||
chr1:214627871 | T | C | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1069-1175T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214627871 | |||||||
chr1:214628295 | G | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-751G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628295 | |||||||
chr1:214628299 | C | T | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1069-747C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628299 | |||||||
chr1:214628477 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1069-569C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628477 | |||||||
chr1:214628569 | C | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1069-477C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628569 | |||||||
chr1:214628591 | A | T | 35 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(32): Show |
48 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.1069-455A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628591 | |||||||
chr1:214628601 | C | T | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-445C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628601 | |||||||
chr1:214628669 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1069-377G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628669 | |||||||
chr1:214628677 | A | T | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1069-369A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628677 | |||||||
chr1:214628917 | C | A | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1069-129C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628917 | |||||||
chr1:214628956 | C | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1069-90C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628956 | |||||||
chr1:214628981 | C | G | 1 | a0017c0020t0006g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1069-65C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 7/19 | chr1 | 214628981 | |||||||
chr1:214629344 | T | C | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+173T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629344 | |||||||
chr1:214629353 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1194+182A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629353 | |||||||
chr1:214629460 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+289T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629460 | |||||||
chr1:214629481 | G | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+310G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629481 | |||||||
chr1:214629514 | T | A | 2 | a0006c0007t0002g0048 a0006c0007t0002g0050 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1194+343T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629514 | |||||||
chr1:214629516 | A | C | 1 | a0015c0024t0002g0014 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1194+345A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629516 | |||||||
chr1:214629518 | A | T | 5 | a0016c0029t0004g0028 a0016c0029t0004g0029 a0033c0049t0004g0052 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+347A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629518 | |||||||
chr1:214629558 | A | AT | 9 | a0001c0001t0001g0179 a0012c0015t0004g0053 a0012c0015t0004g0054 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1194+398dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 214629558 | ||||||
chr1:214629558 | A | ATATTTTT others(7): Show |
2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+388_1194+389i others(16): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 214629558 | ||||||
chr1:214629568 | T | C | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1194+397T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629568 | |||||||
chr1:214629582 | C | T | 2 | a0026c0044t0003g0206 a0029c0045t0003g0207 |
2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1194+411C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629582 | |||||||
chr1:214629608 | A | G | 2 | a0023c0023t0001g0086 a0023c0023t0001g0166 |
2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1194+437A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629608 | |||||||
chr1:214629748 | T | C | 41 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(38): Show |
55 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1194+577T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629748 | |||||||
chr1:214629771 | C | T | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1194+600C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629771 | |||||||
chr1:214629793 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1194+622T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629793 | |||||||
chr1:214629924 | T | A | 20 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(17): Show |
29 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1195-610T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629924 | |||||||
chr1:214629965 | T | G | 4 | a0005c0005t0003g0005 a0005c0005t0003g0210 a0005c0005t0003g0214 others(1): Show |
8 | HG01993.hp1 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195-569T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214629965 | |||||||
chr1:214630134 | AAAG | A | 11 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(8): Show |
15 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195-399_1195-397d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630134 | |||||||
chr1:214630178 | A | G | 1 | a0047c0054t0002g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1195-356A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630178 | |||||||
chr1:214630202 | T | C | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1195-332T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630202 | |||||||
chr1:214630306 | T | C | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1195-228T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630306 | |||||||
chr1:214630404 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1195-130G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630404 | |||||||
chr1:214630416 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1195-118A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630416 | |||||||
chr1:214630502 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1195-32T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 8/19 | chr1 | 214630502 | |||||||
chr1:214630698 | C | A | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1323+36C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630698 | |||||||
chr1:214630766 | G | A | 3 | a0017c0020t0006g0186 a0017c0020t0006g0187 a0017c0020t0006g0188 |
3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1323+104G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630766 | |||||||
chr1:214630941 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+279T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214630941 | |||||||
chr1:214631010 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1323+348A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631010 | |||||||
chr1:214631066 | A | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1323+404A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631066 | |||||||
chr1:214631076 | G | A | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1323+414G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631076 | |||||||
chr1:214631297 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+635C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631297 | |||||||
chr1:214631298 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+636A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631298 | |||||||
chr1:214631299 | C | G | 1 | a0006c0007t0002g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1323+637C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631299 | |||||||
chr1:214631305 | T | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+643T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631305 | |||||||
chr1:214631390 | CTT | C | 6 | a0004c0004t0002g0024 a0004c0004t0002g0185 a0004c0004t0002g0189 others(3): Show |
7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+730_1323+731d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr1 | 214631390 | ||||||
chr1:214631571 | C | T | 2 | a0007c0012t0001g0008 a0007c0012t0001g0087 |
4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+909C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631571 | |||||||
chr1:214631635 | G | A | 2 | a0023c0023t0001g0086 a0023c0023t0001g0166 |
2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1324-845G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631635 | |||||||
chr1:214631644 | C | T | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1324-836C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631644 | |||||||
chr1:214631719 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1324-761C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631719 | |||||||
chr1:214631817 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0169 a0001c0001t0009g0023 |
3 | HG00408.hp1 HG00423.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1324-663C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631817 | |||||||
chr1:214631899 | C | T | 1 | a0032c0035t0002g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1324-581C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631899 | |||||||
chr1:214631913 | G | A | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1324-567G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631913 | |||||||
chr1:214631922 | G | A | 4 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0018c0019t0001g0083 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-558G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214631922 | |||||||
chr1:214632113 | A | C | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1324-367A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632113 | |||||||
chr1:214632140 | G | GA | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-336dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr1 | 214632140 | ||||||
chr1:214632159 | C | T | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-321C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632159 | |||||||
chr1:214632189 | G | A | 11 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1324-291G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632189 | |||||||
chr1:214632287 | A | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1324-193A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632287 | |||||||
chr1:214632290 | C | T | 3 | a0004c0033t0002g0039 a0013c0034t0014g0041 a0032c0035t0002g0040 |
3 | HG00642.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324-190C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632290 | |||||||
chr1:214632442 | A | G | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-38A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 9/19 | chr1 | 214632442 | |||||||
chr1:214632729 | GAAGT | G | 21 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(18): Show |
30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1446+133_1446+136d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214632729 | ||||||
chr1:214632940 | G | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+338G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214632940 | |||||||
chr1:214633062 | TAAAC | T | 6 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1446+464_1446+467d others(6): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214633062 | ||||||
chr1:214633078 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+476C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633078 | |||||||
chr1:214633123 | C | A | 3 | a0006c0007t0002g0047 a0006c0007t0002g0049 a0006c0030t0002g0013 |
4 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+521C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633123 | |||||||
chr1:214633133 | T | C | 44 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(41): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1446+531T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633133 | |||||||
chr1:214633188 | G | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+586G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633188 | |||||||
chr1:214633222 | T | C | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+620T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633222 | |||||||
chr1:214633388 | A | G | 1 | a0004c0004t0002g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1446+786A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633388 | |||||||
chr1:214633564 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1446+962A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633564 | |||||||
chr1:214633611 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0168 a0020c0027t0001g0121 others(1): Show |
4 | HG01081.hp2 HG01261.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1009C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633611 | |||||||
chr1:214633715 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1446+1113G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633715 | |||||||
chr1:214633734 | A | AC | 74 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(71): Show |
90 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1446+1133dupC | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214633734 | ||||||
chr1:214633782 | G | A | 10 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(7): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1446+1180G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633782 | |||||||
chr1:214633934 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1446+1332C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214633934 | |||||||
chr1:214634057 | C | T | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1455C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634057 | |||||||
chr1:214634083 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+1481C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634083 | |||||||
chr1:214634100 | G | A | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1446+1498G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634100 | |||||||
chr1:214634130 | C | A | 44 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(41): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1446+1528C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634130 | |||||||
chr1:214634172 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+1570C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634172 | |||||||
chr1:214634231 | G | C | 4 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0018c0019t0001g0083 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1629G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634231 | |||||||
chr1:214634327 | G | A | 14 | a0004c0004t0002g0025 a0004c0004t0002g0026 a0004c0004t0002g0193 others(11): Show |
15 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+1725G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634327 | |||||||
chr1:214634366 | C | G | 21 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(18): Show |
30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1446+1764C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634366 | |||||||
chr1:214634457 | C | T | 1 | a0005c0005t0003g0215 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1446+1855C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634457 | |||||||
chr1:214634458 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(217): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1446+1856A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634458 | |||||||
chr1:214634756 | A | G | 5 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(2): Show |
5 | HG02717.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+2154A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634756 | |||||||
chr1:214634777 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1446+2175A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634777 | |||||||
chr1:214634951 | T | C | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+2349T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214634951 | |||||||
chr1:214635064 | G | A | 2 | a0002c0002t0005g0016 a0002c0002t0005g0104 |
3 | HG00639.hp2 HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1446+2462G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635064 | |||||||
chr1:214635079 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1446+2477C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635079 | |||||||
chr1:214635210 | T | A | 1 | a0013c0018t0002g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1446+2608T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635210 | |||||||
chr1:214635238 | A | G | 6 | a0004c0004t0002g0024 a0004c0004t0002g0185 a0004c0004t0002g0189 others(3): Show |
7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1447-2628A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635238 | |||||||
chr1:214635680 | C | T | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1447-2186C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635680 | |||||||
chr1:214635770 | T | A | 10 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(7): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1447-2096T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635770 | |||||||
chr1:214635807 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1447-2059T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635807 | |||||||
chr1:214635869 | G | C | 1 | a0015c0055t0002g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1447-1997G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635869 | |||||||
chr1:214635991 | T | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1447-1875T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214635991 | |||||||
chr1:214636087 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1447-1779C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636087 | |||||||
chr1:214636156 | T | C | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1710T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636156 | |||||||
chr1:214636173 | C | T | 1 | a0002c0002t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1447-1693C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636173 | |||||||
chr1:214636221 | A | G | 2 | a0007c0012t0001g0008 a0007c0012t0001g0087 |
4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-1645A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636221 | |||||||
chr1:214636684 | C | T | 1 | a0003c0059t0002g0072 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1447-1182C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636684 | |||||||
chr1:214636764 | C | T | 2 | a0012c0015t0004g0053 a0012c0015t0004g0054 |
2 | HG01109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1447-1102C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636764 | |||||||
chr1:214636839 | C | T | 1 | a0004c0013t0002g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1447-1027C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636839 | |||||||
chr1:214636938 | G | C | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447-928G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214636938 | |||||||
chr1:214637191 | C | T | 1 | a0016c0052t0001g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-675C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637191 | |||||||
chr1:214637324 | T | C | 29 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(26): Show |
31 | HG00642.hp2 HG01109.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1447-542T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637324 | |||||||
chr1:214637425 | T | G | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1447-441T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637425 | |||||||
chr1:214637465 | A | AT | 29 | a0002c0002t0001g0183 a0005c0005t0003g0005 a0005c0005t0003g0012 others(26): Show |
39 | HG01070.hp1 HG01106.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1447-386dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 214637465 | ||||||
chr1:214637511 | G | A | 1 | a0002c0002t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1447-355G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637511 | |||||||
chr1:214637534 | A | G | 4 | a0011c0014t0002g0031 a0011c0014t0002g0032 a0011c0014t0002g0033 others(1): Show |
4 | HG01106.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-332A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637534 | |||||||
chr1:214637607 | G | A | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1447-259G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637607 | |||||||
chr1:214637739 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0011g0173 |
2 | HG02040.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1447-127G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637739 | |||||||
chr1:214637831 | G | A | 21 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(18): Show |
30 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1447-35G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 10/19 | chr1 | 214637831 | |||||||
chr1:214638181 | G | C | 4 | a0005c0005t0003g0005 a0005c0005t0003g0210 a0005c0005t0003g0214 others(1): Show |
8 | HG01993.hp1 NA18943.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+180G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638181 | |||||||
chr1:214638502 | C | G | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1582+501C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638502 | |||||||
chr1:214638519 | C | G | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1582+518C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638519 | |||||||
chr1:214638605 | A | G | 42 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(39): Show |
56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582+604A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638605 | |||||||
chr1:214638688 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1582+687C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638688 | |||||||
chr1:214638697 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0142 |
3 | HG02723.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1582+696G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638697 | |||||||
chr1:214638742 | C | A | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1582+741C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638742 | |||||||
chr1:214638782 | C | T | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1582+781C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638782 | |||||||
chr1:214638783 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1582+782G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638783 | |||||||
chr1:214638873 | G | T | 1 | a0004c0013t0002g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1582+872G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638873 | |||||||
chr1:214638921 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1582+920C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638921 | |||||||
chr1:214638939 | G | A | 42 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(39): Show |
56 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.1582+938G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214638939 | |||||||
chr1:214639246 | T | A | 1 | a0023c0023t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1583-675T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639246 | |||||||
chr1:214639567 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1583-354A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639567 | |||||||
chr1:214639633 | A | G | 3 | a0013c0018t0002g0195 a0013c0018t0002g0199 a0013c0018t0002g0205 |
3 | HG02630.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1583-288A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639633 | |||||||
chr1:214639718 | A | G | 144 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(141): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1583-203A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639718 | |||||||
chr1:214639729 | T | C | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1583-192T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 11/19 | chr1 | 214639729 | |||||||
chr1:214643372 | G | A | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+48G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643372 | |||||||
chr1:214643375 | C | T | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.4986+51C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643375 | |||||||
chr1:214643499 | A | T | 2 | a0016c0029t0004g0028 a0016c0029t0004g0029 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4986+175A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643499 | |||||||
chr1:214643601 | G | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4986+277G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643601 | |||||||
chr1:214643688 | T | TATG | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+365_4986+367d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr1 | 214643688 | ||||||
chr1:214643740 | A | G | 2 | a0007c0012t0001g0008 a0007c0012t0001g0087 |
4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4986+416A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643740 | |||||||
chr1:214643765 | C | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+441C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643765 | |||||||
chr1:214643791 | T | A | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4986+467T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643791 | |||||||
chr1:214643852 | G | A | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+528G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643852 | |||||||
chr1:214643888 | T | A | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4986+564T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214643888 | |||||||
chr1:214644021 | T | C | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4987-536T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644021 | |||||||
chr1:214644111 | G | A | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4987-446G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644111 | |||||||
chr1:214644131 | G | A | 3 | a0017c0020t0006g0186 a0017c0020t0006g0187 a0017c0020t0006g0188 |
3 | HG02486.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4987-426G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644131 | |||||||
chr1:214644228 | A | G | 28 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(25): Show |
38 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.4987-329A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644228 | |||||||
chr1:214644378 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0142 |
3 | HG02723.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4987-179C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644378 | |||||||
chr1:214644513 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4987-44T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 12/19 | chr1 | 214644513 | |||||||
chr1:214647590 | A | G | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7830+190A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647590 | |||||||
chr1:214647657 | G | A | 1 | a0013c0018t0002g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7830+257G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647657 | |||||||
chr1:214647877 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7830+477A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214647877 | |||||||
chr1:214648029 | G | A | 1 | a0004c0004t0002g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7830+629G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648029 | |||||||
chr1:214648048 | G | C | 2 | a0019c0022t0001g0113 a0028c0031t0001g0175 |
2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.7831-627G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648048 | |||||||
chr1:214648072 | A | C | 32 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(29): Show |
42 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.7831-603A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648072 | |||||||
chr1:214648113 | C | G | 40 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(37): Show |
54 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.7831-562C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648113 | |||||||
chr1:214648166 | G | T | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7831-509G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648166 | |||||||
chr1:214648287 | T | C | 1 | a0008c0006t0001g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.7831-388T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648287 | |||||||
chr1:214648318 | A | G | 6 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.7831-357A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648318 | |||||||
chr1:214648337 | G | C | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-338G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648337 | |||||||
chr1:214648356 | TA | T | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-317delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr1 | 214648356 | ||||||
chr1:214648472 | A | C | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.7831-203A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648472 | |||||||
chr1:214648546 | C | T | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7831-129C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648546 | |||||||
chr1:214648616 | G | A | 22 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.7831-59G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 13/19 | chr1 | 214648616 | |||||||
chr1:214648916 | T | C | 1 | a0008c0006t0001g0085 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7983+89T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214648916 | |||||||
chr1:214649098 | C | T | 6 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(3): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.7983+271C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649098 | |||||||
chr1:214649106 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.7983+279C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649106 | |||||||
chr1:214649170 | G | A | 1 | a0003c0003t0002g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.7983+343G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649170 | |||||||
chr1:214649316 | G | A | 6 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.7983+489G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649316 | |||||||
chr1:214649326 | C | G | 19 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(16): Show |
21 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.7983+499C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649326 | |||||||
chr1:214649493 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.7983+666T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649493 | |||||||
chr1:214649559 | G | T | 9 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0048 others(6): Show |
13 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.7983+732G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214649559 | |||||||
chr1:214650072 | T | A | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7983+1245T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650072 | |||||||
chr1:214650111 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7983+1284A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650111 | |||||||
chr1:214650145 | T | C | 8 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.7983+1318T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650145 | |||||||
chr1:214650201 | G | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7983+1374G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650201 | |||||||
chr1:214650203 | T | G | 85 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(82): Show |
107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.7983+1376T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650203 | |||||||
chr1:214650358 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.7984-1352G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650358 | |||||||
chr1:214650461 | C | T | 2 | a0001c0001t0001g0176 a0041c0041t0001g0177 |
2 | HG00544.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7984-1249C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650461 | |||||||
chr1:214650505 | A | G | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7984-1205A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650505 | |||||||
chr1:214650550 | A | G | 20 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(17): Show |
22 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.7984-1160A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650550 | |||||||
chr1:214650579 | C | T | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.7984-1131C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650579 | |||||||
chr1:214650667 | C | T | 30 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(27): Show |
40 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.7984-1043C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650667 | |||||||
chr1:214650738 | C | CA | 18 | a0004c0004t0002g0024 a0004c0004t0002g0025 a0004c0004t0002g0026 others(15): Show |
20 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.7984-965dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 214650738 | ||||||
chr1:214650774 | A | G | 1 | a0001c0001t0001g0011 | 3 | HG02698.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.7984-936A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650774 | |||||||
chr1:214650814 | A | G | 8 | a0015c0024t0002g0014 a0017c0020t0006g0186 a0017c0020t0006g0187 others(5): Show |
9 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.7984-896A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650814 | |||||||
chr1:214650999 | G | C | 1 | a0032c0035t0002g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7984-711G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214650999 | |||||||
chr1:214651050 | C | A | 44 | a0003c0003t0002g0002 a0003c0003t0002g0015 a0003c0003t0002g0061 others(41): Show |
63 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.7984-660C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651050 | |||||||
chr1:214651088 | G | T | 1 | a0003c0003t0002g0071 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.7984-622G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651088 | |||||||
chr1:214651193 | A | G | 12 | a0005c0005t0003g0005 a0005c0005t0003g0012 a0005c0005t0003g0209 others(9): Show |
18 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.7984-517A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651193 | |||||||
chr1:214651326 | C | T | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7984-384C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651326 | |||||||
chr1:214651334 | A | G | 1 | a0006c0007t0002g0006 | 4 | HG02109.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.7984-376A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651334 | |||||||
chr1:214651464 | A | G | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.7984-246A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651464 | |||||||
chr1:214651476 | G | A | 2 | a0004c0033t0002g0039 a0013c0034t0014g0041 |
2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.7984-234G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651476 | |||||||
chr1:214651496 | G | A | 1 | a0021c0028t0002g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7984-214G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651496 | |||||||
chr1:214651561 | A | G | 2 | a0004c0033t0002g0039 a0013c0034t0014g0041 |
2 | HG00642.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.7984-149A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651561 | |||||||
chr1:214651637 | T | C | 1 | a0024c0026t0002g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7984-73T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 14/19 | chr1 | 214651637 | |||||||
chr1:214651946 | C | CT | 6 | a0004c0004t0002g0024 a0004c0004t0002g0185 a0004c0004t0002g0189 others(3): Show |
7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.8160+72dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214651946 | ||||||
chr1:214651946 | C | CTT | 48 | a0004c0004t0002g0025 a0004c0004t0002g0026 a0004c0004t0002g0193 others(45): Show |
59 | HG01346.hp2 HG01358.hp1 HG01496.hp1 others(56): Show |
intron_variant | MODIFIER | c.8160+71_8160+72dup others(2): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214651946 | ||||||
chr1:214652068 | A | AT | 5 | a0001c0042t0001g0153 a0003c0003t0002g0075 a0007c0009t0001g0129 others(2): Show |
5 | HG03239.hp1 HG03516.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.8160+200dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | ||||||
chr1:214652068 | A | ATTTTT | 14 | a0004c0004t0002g0024 a0004c0004t0002g0026 a0004c0004t0002g0185 others(11): Show |
16 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.8160+196_8160+200d others(7): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | ||||||
chr1:214652068 | A | ATTTTTTT | 4 | a0006c0007t0002g0006 a0006c0007t0002g0047 a0006c0007t0002g0049 others(1): Show |
8 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.8160+194_8160+200d others(9): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | ||||||
chr1:214652068 | AT | A | 51 | a0001c0001t0001g0022 a0001c0001t0001g0159 a0002c0002t0001g0003 others(48): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.8160+200delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | ||||||
chr1:214652068 | ATT | A | 32 | a0002c0002t0001g0093 a0004c0013t0002g0042 a0004c0013t0002g0043 others(29): Show |
39 | HG00140.hp1 HG01346.hp2 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.8160+199_8160+200d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652068 | ||||||
chr1:214652121 | C | T | 2 | a0024c0026t0002g0035 a0024c0026t0002g0051 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.8160+235C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652121 | |||||||
chr1:214652146 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.8160+260C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652146 | |||||||
chr1:214652185 | G | A | 12 | a0003c0003t0002g0065 a0005c0005t0003g0005 a0005c0005t0003g0012 others(9): Show |
18 | HG01074.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8160+299G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652185 | |||||||
chr1:214652211 | A | G | 1 | a0003c0003t0013g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.8160+325A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652211 | |||||||
chr1:214652222 | T | A | 1 | a0045c0050t0004g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8160+336T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652222 | |||||||
chr1:214652229 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0002c0002t0001g0101 |
3 | HG01943.hp1 NA18612.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.8160+343G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652229 | |||||||
chr1:214652233 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0009g0023 |
2 | HG00408.hp1 HG00423.hp2 |
intron_variant | MODIFIER | c.8160+347C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652233 | |||||||
chr1:214652234 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0009g0023 |
2 | HG00408.hp1 HG00423.hp2 |
intron_variant | MODIFIER | c.8160+348A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652234 | |||||||
chr1:214652236 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
8 | HG00408.hp1 HG00423.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.8160+350T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652236 | |||||||
chr1:214652237 | G | A | 1 | a0003c0059t0002g0072 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.8160+351G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652237 | |||||||
chr1:214652242 | A | G | 1 | a0004c0004t0002g0197 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8160+356A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652242 | |||||||
chr1:214652267 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.8160+381T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652267 | |||||||
chr1:214652294 | C | T | 1 | a0002c0032t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.8160+408C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652294 | |||||||
chr1:214652326 | C | T | 58 | a0001c0001t0001g0151 a0002c0002t0001g0003 a0002c0002t0001g0004 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.8160+440C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652326 | |||||||
chr1:214652380 | A | G | 4 | a0013c0034t0014g0041 a0015c0024t0002g0014 a0021c0028t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02257.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8161-448A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652380 | |||||||
chr1:214652408 | C | T | 12 | a0001c0001t0008g0172 a0005c0005t0003g0005 a0005c0005t0003g0012 others(9): Show |
18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8161-420C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652408 | |||||||
chr1:214652411 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.8161-417G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652411 | |||||||
chr1:214652444 | CT | C | 107 | a0001c0001t0001g0095 a0001c0001t0001g0132 a0001c0001t0001g0142 others(104): Show |
131 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.8161-367delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652444 | ||||||
chr1:214652444 | CTT | C | 8 | a0002c0002t0001g0099 a0002c0002t0001g0183 a0002c0002t0002g0208 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.8161-368_8161-367d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 214652444 | ||||||
chr1:214652455 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8161-373T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652455 | |||||||
chr1:214652471 | C | T | 60 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(57): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.8161-357C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652471 | |||||||
chr1:214652505 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.8161-323A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652505 | |||||||
chr1:214652529 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(206): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.8161-299T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652529 | |||||||
chr1:214652589 | G | A | 2 | a0005c0005t0003g0012 a0005c0005t0003g0216 |
4 | HG01346.hp2 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.8161-239G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652589 | |||||||
chr1:214652632 | CAG | C | 62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(59): Show |
75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.8161-195_8161-194d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652632 | |||||||
chr1:214652742 | T | C | 12 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(9): Show |
15 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.8161-86T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 15/19 | chr1 | 214652742 | |||||||
chr1:214653021 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.8322+32G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653021 | |||||||
chr1:214653028 | T | G | 1 | a0016c0052t0001g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8322+39T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653028 | |||||||
chr1:214653127 | C | A | 13 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(10): Show |
16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+138C>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653127 | |||||||
chr1:214653249 | T | C | 3 | a0003c0003t0002g0063 a0003c0003t0002g0068 a0003c0003t0002g0071 |
3 | HG02135.hp2 NA18966.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8322+260T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653249 | |||||||
chr1:214653309 | G | C | 6 | a0021c0028t0002g0200 a0021c0028t0002g0201 a0022c0025t0002g0204 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.8322+320G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653309 | |||||||
chr1:214653311 | C | T | 13 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(10): Show |
16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+322C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653311 | |||||||
chr1:214653365 | C | T | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8322+376C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653365 | |||||||
chr1:214653423 | C | T | 6 | a0004c0004t0002g0024 a0004c0004t0002g0185 a0004c0004t0002g0189 others(3): Show |
7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.8322+434C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653423 | |||||||
chr1:214653434 | TCTC | T | 4 | a0009c0010t0001g0009 a0009c0010t0001g0123 a0009c0010t0001g0125 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.8322+449_8322+451d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653434 | ||||||
chr1:214653466 | ACT | A | 4 | a0009c0010t0001g0009 a0009c0010t0001g0123 a0009c0010t0001g0125 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.8322+478_8322+479d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653466 | |||||||
chr1:214653467 | CT | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.8322+493delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653467 | ||||||
chr1:214653467 | CTTT | C | 13 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(10): Show |
16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+491_8322+493d others(5): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214653467 | ||||||
chr1:214653482 | T | A | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8322+493T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653482 | |||||||
chr1:214653614 | G | A | 13 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(10): Show |
16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+625G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653614 | |||||||
chr1:214653645 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.8322+656A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653645 | |||||||
chr1:214653696 | G | A | 1 | a0043c0043t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8322+707G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653696 | |||||||
chr1:214653719 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(109): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.8322+730G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653719 | |||||||
chr1:214653723 | C | T | 13 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(10): Show |
16 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8322+734C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653723 | |||||||
chr1:214653934 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(187): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.8322+945A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214653934 | |||||||
chr1:214654070 | T | C | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8322+1081T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654070 | |||||||
chr1:214654177 | A | G | 1 | a0019c0022t0001g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.8323-1064A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654177 | |||||||
chr1:214654188 | C | T | 1 | a0004c0033t0002g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8323-1053C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654188 | |||||||
chr1:214654360 | G | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0021 others(49): Show |
62 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.8323-881G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654360 | |||||||
chr1:214654362 | C | T | 1 | a0039c0047t0002g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.8323-879C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654362 | |||||||
chr1:214654404 | C | G | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8323-837C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654404 | |||||||
chr1:214654441 | C | T | 25 | a0004c0004t0002g0025 a0004c0004t0002g0026 a0004c0004t0002g0193 others(22): Show |
29 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.8323-800C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654441 | |||||||
chr1:214654516 | A | G | 11 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(8): Show |
14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-725A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654516 | |||||||
chr1:214654518 | G | C | 2 | a0021c0028t0002g0200 a0021c0028t0002g0201 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8323-723G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654518 | |||||||
chr1:214654960 | T | C | 11 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(8): Show |
14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-281T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214654960 | |||||||
chr1:214654965 | T | TA | 11 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(8): Show |
14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-273dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214654965 | ||||||
chr1:214655007 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8323-234T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655007 | |||||||
chr1:214655015 | A | G | 8 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(5): Show |
9 | HG00642.hp2 HG02145.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.8323-226A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655015 | |||||||
chr1:214655090 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.8323-151C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | chr1 | 214655090 | |||||||
chr1:214655178 | A | AT | 11 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(8): Show |
14 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.8323-58dupT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 214655178 | ||||||
chr1:214655469 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8485+66A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655469 | |||||||
chr1:214655545 | A | G | 10 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(7): Show |
13 | HG00642.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.8485+142A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655545 | |||||||
chr1:214655624 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.8485+221A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655624 | |||||||
chr1:214655667 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+264G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655667 | |||||||
chr1:214655694 | G | A | 2 | a0015c0055t0002g0030 a0041c0041t0001g0177 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.8485+291G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655694 | |||||||
chr1:214655748 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+345A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655748 | |||||||
chr1:214655752 | G | A | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8485+349G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655752 | |||||||
chr1:214655769 | T | C | 1 | a0005c0005t0003g0215 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.8485+366T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655769 | |||||||
chr1:214655851 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.8485+448A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655851 | |||||||
chr1:214655866 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.8485+463T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655866 | |||||||
chr1:214655877 | C | T | 1 | a0004c0013t0002g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8485+474C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214655877 | |||||||
chr1:214656028 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8485+625C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656028 | |||||||
chr1:214656056 | G | C | 14 | a0004c0004t0002g0025 a0004c0004t0002g0026 a0004c0004t0002g0193 others(11): Show |
15 | HG02145.hp2 HG02572.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.8485+653G>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656056 | |||||||
chr1:214656235 | G | A | 2 | a0004c0004t0002g0202 a0007c0009t0001g0156 |
2 | HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8486-698G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656235 | |||||||
chr1:214656268 | G | A | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8486-665G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656268 | |||||||
chr1:214656305 | A | G | 1 | a0045c0050t0004g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8486-628A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656305 | |||||||
chr1:214656342 | T | A | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8486-591T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656342 | |||||||
chr1:214656448 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-485T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656448 | |||||||
chr1:214656465 | A | G | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8486-468A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656465 | |||||||
chr1:214656573 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-360T>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656573 | |||||||
chr1:214656630 | A | T | 1 | a0010c0008t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.8486-303A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656630 | |||||||
chr1:214656657 | G | A | 2 | a0016c0052t0001g0154 a0036c0051t0001g0178 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.8486-276G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656657 | |||||||
chr1:214656682 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.8486-251G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656682 | |||||||
chr1:214656799 | A | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.8486-134A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656799 | |||||||
chr1:214656822 | T | TA | 11 | a0004c0013t0002g0042 a0004c0013t0002g0043 a0004c0013t0002g0044 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.8486-100dupA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 214656822 | ||||||
chr1:214656822 | TA | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.8486-100delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 214656822 | ||||||
chr1:214656863 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8486-70G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656863 | |||||||
chr1:214656872 | T | C | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8486-61T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 17/19 | chr1 | 214656872 | |||||||
chr1:214657565 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.8962+156A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657565 | |||||||
chr1:214657662 | T | C | 2 | a0007c0012t0001g0008 a0007c0012t0001g0087 |
4 | HG02622.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.8962+253T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657662 | |||||||
chr1:214657706 | G | A | 12 | a0001c0001t0008g0172 a0005c0005t0003g0005 a0005c0005t0003g0012 others(9): Show |
18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8962+297G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657706 | |||||||
chr1:214657739 | A | G | 12 | a0001c0001t0008g0172 a0005c0005t0003g0005 a0005c0005t0003g0012 others(9): Show |
18 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.8962+330A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657739 | |||||||
chr1:214657741 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.8962+332C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657741 | |||||||
chr1:214657892 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.8962+483G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657892 | |||||||
chr1:214657918 | A | T | 3 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0047c0054t0002g0184 |
3 | HG02615.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8962+509A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657918 | |||||||
chr1:214657944 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.8962+535A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214657944 | |||||||
chr1:214658062 | C | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(23): Show |
29 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.8962+653C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658062 | |||||||
chr1:214658086 | G | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.8962+677G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658086 | |||||||
chr1:214658186 | GAA | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.8963-658_8963-657d others(4): Show |
CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 214658186 | ||||||
chr1:214658334 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0149 |
2 | NA18950.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.8963-516C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658334 | |||||||
chr1:214658336 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.8963-514T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658336 | |||||||
chr1:214658487 | T | A | 1 | a0004c0013t0002g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8963-363T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658487 | |||||||
chr1:214658556 | A | G | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8963-294A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658556 | |||||||
chr1:214658586 | A | T | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8963-264A>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 18/19 | chr1 | 214658586 | |||||||
chr1:214659168 | G | A | 2 | a0022c0025t0002g0204 a0022c0025t0012g0203 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.9141+140G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659168 | |||||||
chr1:214659204 | A | G | 1 | a0013c0034t0014g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+176A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659204 | |||||||
chr1:214659446 | TA | T | 31 | a0001c0001t0008g0172 a0004c0013t0002g0042 a0004c0013t0002g0043 others(28): Show |
38 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.9141+431delA | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 214659446 | ||||||
chr1:214659522 | G | T | 1 | a0045c0050t0004g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.9141+494G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659522 | |||||||
chr1:214659833 | C | G | 1 | a0035c0061t0004g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.9141+805C>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659833 | |||||||
chr1:214659940 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.9141+912G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659940 | |||||||
chr1:214659945 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9141+917C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214659945 | |||||||
chr1:214660082 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(110): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.9141+1054G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660082 | |||||||
chr1:214660127 | A | G | 6 | a0004c0004t0002g0024 a0004c0004t0002g0185 a0004c0004t0002g0189 others(3): Show |
7 | HG01109.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.9141+1099A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660127 | |||||||
chr1:214660191 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.9141+1163A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660191 | |||||||
chr1:214660365 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9141+1337C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660365 | |||||||
chr1:214660379 | C | T | 25 | a0001c0001t0008g0172 a0003c0003t0013g0070 a0005c0005t0003g0005 others(22): Show |
31 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.9141+1351C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660379 | |||||||
chr1:214660517 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9141+1489C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660517 | |||||||
chr1:214660755 | A | G | 3 | a0018c0019t0001g0081 a0018c0019t0001g0082 a0047c0054t0002g0184 |
3 | HG02615.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.9141+1727A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660755 | |||||||
chr1:214660846 | G | A | 2 | a0015c0055t0002g0030 a0041c0041t0001g0177 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9141+1818G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214660846 | |||||||
chr1:214661017 | C | T | 2 | a0011c0014t0002g0032 a0011c0014t0002g0034 |
2 | HG01106.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.9141+1989C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661017 | |||||||
chr1:214661048 | C | T | 6 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.9141+2020C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661048 | |||||||
chr1:214661055 | C | T | 1 | a0013c0034t0014g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+2027C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661055 | |||||||
chr1:214661247 | A | G | 1 | a0013c0034t0014g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9141+2219A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661247 | |||||||
chr1:214661313 | A | G | 2 | a0015c0055t0002g0030 a0041c0041t0001g0177 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.9142-2278A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661313 | |||||||
chr1:214661452 | A | C | 1 | a0037c0053t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9142-2139A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661452 | |||||||
chr1:214661505 | C | T | 1 | a0006c0007t0002g0050 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9142-2086C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661505 | |||||||
chr1:214661604 | C | T | 1 | a0013c0034t0014g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9142-1987C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661604 | |||||||
chr1:214661755 | G | T | 1 | a0022c0025t0002g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.9142-1836G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661755 | |||||||
chr1:214661833 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9142-1758T>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214661833 | |||||||
chr1:214661874 | CT | C | 33 | a0001c0001t0001g0019 a0001c0001t0001g0094 a0001c0001t0001g0141 others(30): Show |
40 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.9142-1706delT | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 214661874 | ||||||
chr1:214662311 | G | A | 1 | a0002c0002t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.9142-1280G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662311 | |||||||
chr1:214662412 | G | T | 1 | a0002c0002t0001g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9142-1179G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662412 | |||||||
chr1:214662515 | T | C | 1 | a0031c0056t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.9142-1076T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662515 | |||||||
chr1:214662655 | T | C | 2 | a0026c0044t0003g0206 a0029c0045t0003g0207 |
2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.9142-936T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662655 | |||||||
chr1:214662719 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9142-872A>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662719 | |||||||
chr1:214662873 | G | A | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9142-718G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662873 | |||||||
chr1:214662878 | C | T | 1 | a0038c0058t0002g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9142-713C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662878 | |||||||
chr1:214662883 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.9142-708G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662883 | |||||||
chr1:214662925 | G | A | 11 | a0012c0015t0004g0053 a0012c0015t0004g0054 a0012c0015t0004g0055 others(8): Show |
11 | HG01109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.9142-666G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214662925 | |||||||
chr1:214663035 | G | A | 1 | a0040c0046t0002g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9142-556G>A | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663035 | |||||||
chr1:214663113 | A | G | 13 | a0001c0001t0008g0172 a0003c0003t0013g0070 a0005c0005t0003g0005 others(10): Show |
19 | HG00423.hp1 HG01346.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.9142-478A>G | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663113 | |||||||
chr1:214663157 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.9142-434T>C | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663157 | |||||||
chr1:214663525 | C | T | 2 | a0004c0004t0002g0196 a0004c0004t0002g0197 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.9142-66C>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663525 | |||||||
chr1:214663575 | G | T | 1 | a0004c0013t0002g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9142-16G>T | CENPF | ENSG00000117724.15 | transcript | ENST00000366955.8 | protein_coding | 19/19 | chr1 | 214663575 |