Item | Value |
---|---|
geneid | 51668 |
ensemblid | ENSG00000081870.12 |
hgncid | 25019 |
symbol | IFT25 |
name | intraflagellar transport 25 |
refseq_nuc | NM_016126.4 |
refseq_prot | NP_057210.2 |
ensembl_nuc | ENST00000194214.10 |
ensembl_prot | ENSP00000194214.5 |
mane_status | MANE Select |
chr | chr1 |
start | 53921561 |
end | 53945699 |
strand | - |
ver | v1.2 |
region | chr1:53921561-53945699 |
region5000 | chr1:53916561-53950699 |
regionname0 | IFT25_chr1_53921561_53945699 |
regionname5000 | IFT25_chr1_53916561_53950699 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 144 | 281 | 94 | 37 | 110 | 12 | 26 | 80 | IFT25_chr1_53916561_53950699 | IFT25 | MRKID others(139): Show |
chr1 | 53916561 | 53950699 |
a0002 | 0/0 | 144 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | MRKID others(139): Show |
chr1 | 53916561 | 53950699 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 432 | 280 | 94 | 37 | 109 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | ATGAG others(427): Show |
chr1 | 53916561 | 53950699 | ||
a0001c0003 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | ATGAG others(427): Show |
chr1 | 53916561 | 53950699 | ||
a0002c0002 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | ATGAG others(427): Show |
chr1 | 53916561 | 53950699 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 685 | 274 | 89 | 36 | 109 | 12 | 26 | IFT25_chr1_53916561_53950699 | IFT25 | AGAGT others(680): Show |
chr1 | 53916561 | 53950699 |
a0001c0001t0002 | 0/0 | 685 | 5 | 4 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | AGAGT others(680): Show |
chr1 | 53916561 | 53950699 |
a0001c0001t0003 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | AGAGT others(680): Show |
chr1 | 53916561 | 53950699 |
a0001c0003t0001 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | AGAGT others(680): Show |
chr1 | 53916561 | 53950699 |
a0002c0002t0001 | 0/0 | 685 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | AGAGT others(680): Show |
chr1 | 53916561 | 53950699 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 1 | 4 | 15 | 0 | 3 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0002 | 1/0 | 20 | 1 | 2 | 12 | 2 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0003 | 0/1 | 19 | 1 | 7 | 3 | 3 | 4 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0004 | 0/0 | 9 | 2 | 0 | 4 | 1 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ASW | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | IFT25_chr1_53916561_53950699 | IFT25 | chr1 | 53916561 | 53950699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53923910 | T | G | 1 | a0002 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.312A>C | p.Glu104Asp | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/6 | 472/685 | 312/435 | 104/144 | chr1 | 53923910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53940044 | G | A | 1 | a0001c0003 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.39C>T | p.Ser13Ser | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/6 | 199/685 | 39/435 | 13/144 | chr1 | 53940044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53921615 | A | G | 1 | a0001c0001t0002 | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*36T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 6/6 | 36 | chr1 | 53921615 | ||||||
chr1:53945629 | C | A | 1 | a0001c0001t0002 | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/6 | 5547 | chr1 | 53945629 | ||||||
chr1:53945646 | C | T | 1 | a0001c0001t0003 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/6 | 5564 | chr1 | 53945646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:53921772 | A | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.319-5T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53921772 | |||||||
chr1:53921904 | T | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
83 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.319-137A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53921904 | |||||||
chr1:53922184 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.319-417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922184 | |||||||
chr1:53922390 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA19063.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.319-623C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922390 | |||||||
chr1:53922394 | CA | C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0133 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-628delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | |||||||
chr1:53922394 | CAA | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
78 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.319-629_319-628del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | |||||||
chr1:53922394 | CAAA | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0111 a0001c0001t0001g0112 |
6 | HG02572.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-630_319-628del others(3): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922394 | |||||||
chr1:53922476 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.319-709C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922476 | |||||||
chr1:53922634 | A | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.319-867T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922634 | |||||||
chr1:53922852 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.318+1052C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53922852 | |||||||
chr1:53923163 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.318+741T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923163 | |||||||
chr1:53923297 | T | TAATA | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.318+603_318+606dup others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923297 | |||||||
chr1:53923357 | T | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+547A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923357 | |||||||
chr1:53923413 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+491C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923413 | |||||||
chr1:53923428 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.318+476T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923428 | |||||||
chr1:53923440 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.318+464G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923440 | |||||||
chr1:53923450 | T | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.318+454A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923450 | |||||||
chr1:53923527 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.318+377T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923527 | |||||||
chr1:53923632 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.318+272T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923632 | |||||||
chr1:53923641 | T | A | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.318+263A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923641 | |||||||
chr1:53923741 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0151 |
3 | HG02559.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+163T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923741 | |||||||
chr1:53923798 | C | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
83 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.318+106G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923798 | |||||||
chr1:53923844 | G | GT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.318+59dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 5/5 | chr1 | 53923844 | |||||||
chr1:53923985 | T | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
9 | HG01891.hp1 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.275-38A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53923985 | |||||||
chr1:53924101 | TAG | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(40): Show |
97 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.275-156_275-155del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924101 | |||||||
chr1:53924258 | TA | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-312delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924258 | |||||||
chr1:53924346 | A | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
99 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.275-399T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924346 | |||||||
chr1:53924359 | T | C | 1 | a0001c0001t0001g0023 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.275-412A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924359 | |||||||
chr1:53924404 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0139 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.275-457G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924404 | |||||||
chr1:53924511 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.275-564G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924511 | |||||||
chr1:53924521 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.275-574C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924521 | |||||||
chr1:53924624 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.275-677G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924624 | |||||||
chr1:53924629 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.275-682C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924629 | |||||||
chr1:53924694 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.275-747C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924694 | |||||||
chr1:53924754 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.275-807C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924754 | |||||||
chr1:53924793 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0017 others(16): Show |
47 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.275-846G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924793 | |||||||
chr1:53924861 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.275-914A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924861 | |||||||
chr1:53924927 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.275-980A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53924927 | |||||||
chr1:53925001 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(6): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.275-1054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925001 | |||||||
chr1:53925263 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.275-1316G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925263 | |||||||
chr1:53925319 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.275-1372T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925319 | |||||||
chr1:53925327 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.275-1380A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925327 | |||||||
chr1:53925467 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.275-1520A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925467 | |||||||
chr1:53925558 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.275-1611C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925558 | |||||||
chr1:53925582 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.275-1635C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925582 | |||||||
chr1:53925650 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.275-1703C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925650 | |||||||
chr1:53925888 | G | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-1941C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53925888 | |||||||
chr1:53926001 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-2054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926001 | |||||||
chr1:53926034 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.275-2087C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926034 | |||||||
chr1:53926077 | C | CA | 8 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0001c0001t0001g0119 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2131dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926077 | |||||||
chr1:53926077 | CA | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0080 others(4): Show |
8 | HG01070.hp2 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-2131delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926077 | |||||||
chr1:53926171 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0077 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.274+2201C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926171 | |||||||
chr1:53926198 | T | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.274+2174A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926198 | |||||||
chr1:53926393 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+1979G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926393 | |||||||
chr1:53926529 | TTAATA | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+1838_274+1842d others(7): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926529 | |||||||
chr1:53926565 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.274+1807G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926565 | |||||||
chr1:53926629 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.274+1743G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926629 | |||||||
chr1:53926722 | A | ATT | 11 | a0001c0001t0001g0120 a0001c0001t0001g0132 a0001c0001t0001g0135 others(8): Show |
12 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+1648_274+1649d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926722 | |||||||
chr1:53926857 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1515G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926857 | |||||||
chr1:53926881 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274+1491G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53926881 | |||||||
chr1:53927061 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0119 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.274+1311C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927061 | |||||||
chr1:53927091 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+1281G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927091 | |||||||
chr1:53927186 | TG | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0087 |
3 | HG01496.hp1 HG01934.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.274+1185delC | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927186 | |||||||
chr1:53927235 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.274+1137G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927235 | |||||||
chr1:53927331 | A | G | 28 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0027 others(25): Show |
39 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.274+1041T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927331 | |||||||
chr1:53927349 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.274+1023G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927349 | |||||||
chr1:53927450 | G | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+922C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927450 | |||||||
chr1:53927538 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+834A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927538 | |||||||
chr1:53927770 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.274+602A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927770 | |||||||
chr1:53927819 | C | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.274+553G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927819 | |||||||
chr1:53927838 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+534T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927838 | |||||||
chr1:53927965 | T | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+407A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927965 | |||||||
chr1:53927988 | T | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+384A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53927988 | |||||||
chr1:53928134 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+238G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928134 | |||||||
chr1:53928220 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.274+152A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928220 | |||||||
chr1:53928239 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+133G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928239 | |||||||
chr1:53928342 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
7 | HG02080.hp2 NA18969.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+30A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 4/5 | chr1 | 53928342 | |||||||
chr1:53928464 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.206-24T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928464 | |||||||
chr1:53928468 | T | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-28A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928468 | |||||||
chr1:53928480 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-40A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928480 | |||||||
chr1:53928605 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0133 |
2 | NA19030.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.206-165A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928605 | |||||||
chr1:53928698 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.206-258C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928698 | |||||||
chr1:53928714 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0145 others(1): Show |
10 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.206-274A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928714 | |||||||
chr1:53928757 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.206-317A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928757 | |||||||
chr1:53928768 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-328A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928768 | |||||||
chr1:53928994 | T | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-554A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53928994 | |||||||
chr1:53929062 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0044 others(1): Show |
8 | HG00408.hp2 HG02074.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.206-622A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929062 | |||||||
chr1:53929176 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.206-736C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929176 | |||||||
chr1:53929304 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.205+735G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929304 | |||||||
chr1:53929347 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.205+692C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929347 | |||||||
chr1:53929696 | A | ACT | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+342_205+343ins others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929696 | |||||||
chr1:53929704 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.205+335G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929704 | |||||||
chr1:53929764 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.205+275T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929764 | |||||||
chr1:53929815 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.205+224C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929815 | |||||||
chr1:53929889 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+150G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53929889 | |||||||
chr1:53930000 | CA | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
82 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.205+38delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 3/5 | chr1 | 53930000 | |||||||
chr1:53930215 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.99-70A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930215 | |||||||
chr1:53930410 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-265G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930410 | |||||||
chr1:53930554 | G | GT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0135 a0001c0001t0001g0136 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-410dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930554 | |||||||
chr1:53930577 | G | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-432C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930577 | |||||||
chr1:53930653 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(6): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99-508G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53930653 | |||||||
chr1:53931052 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.99-907G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931052 | |||||||
chr1:53931160 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0109 |
2 | NA18956.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.99-1015T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931160 | |||||||
chr1:53931160 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-1015T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931160 | |||||||
chr1:53931567 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-1422C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931567 | |||||||
chr1:53931729 | C | A | 1 | a0001c0001t0001g0026 | 2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.99-1584G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931729 | |||||||
chr1:53931735 | C | CT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0027 others(25): Show |
39 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.99-1591dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931735 | |||||||
chr1:53931737 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-1592A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931737 | |||||||
chr1:53931807 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.99-1662A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931807 | |||||||
chr1:53931866 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.99-1721T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931866 | |||||||
chr1:53931985 | T | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-1840A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53931985 | |||||||
chr1:53932043 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-1898G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932043 | |||||||
chr1:53932077 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02280.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.99-1932G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932077 | |||||||
chr1:53932104 | C | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0030 others(7): Show |
19 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.99-1959G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932104 | |||||||
chr1:53932179 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-2034G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932179 | |||||||
chr1:53932183 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0085 |
2 | HG01243.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.99-2038A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932183 | |||||||
chr1:53932214 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99-2069C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932214 | |||||||
chr1:53932333 | C | CA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
76 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.99-2189dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932333 | |||||||
chr1:53932405 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99-2260A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932405 | |||||||
chr1:53932407 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99-2262G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932407 | |||||||
chr1:53932473 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99-2328A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932473 | |||||||
chr1:53932494 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99-2349A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932494 | |||||||
chr1:53932522 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2377A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932522 | |||||||
chr1:53932545 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
8 | HG00423.hp2 HG00438.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2400T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932545 | |||||||
chr1:53932648 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-2503A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932648 | |||||||
chr1:53932755 | G | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2610C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932755 | |||||||
chr1:53932787 | C | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-2642G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53932787 | |||||||
chr1:53933106 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99-2961T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933106 | |||||||
chr1:53933135 | C | CT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(11): Show |
23 | HG00099.hp1 HG01070.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.99-2991dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | |||||||
chr1:53933135 | C | CTT | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0132 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-2992_99-2991dup others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | |||||||
chr1:53933135 | CT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0030 others(9): Show |
21 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.99-2991delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933135 | |||||||
chr1:53933159 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.99-3014C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933159 | |||||||
chr1:53933188 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0075 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.99-3043G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933188 | |||||||
chr1:53933220 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3075G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933220 | |||||||
chr1:53933265 | A | G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-3120T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933265 | |||||||
chr1:53933283 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99-3138G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933283 | |||||||
chr1:53933303 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99-3158A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933303 | |||||||
chr1:53933355 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3210G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933355 | |||||||
chr1:53933408 | G | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-3263C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933408 | |||||||
chr1:53933413 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0075 others(1): Show |
6 | HG00738.hp2 HG01106.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-3268G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933413 | |||||||
chr1:53933429 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.99-3284G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933429 | |||||||
chr1:53933562 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99-3417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933562 | |||||||
chr1:53933571 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.99-3426G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933571 | |||||||
chr1:53933832 | A | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0092 |
5 | NA18952.hp1 NA18959.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3687T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933832 | |||||||
chr1:53933853 | AT | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3709delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933853 | |||||||
chr1:53933870 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99-3725G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933870 | |||||||
chr1:53933916 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0104 |
7 | HG00544.hp1 HG03490.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-3771G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53933916 | |||||||
chr1:53934066 | C | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3921G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934066 | |||||||
chr1:53934152 | C | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0121 others(10): Show |
16 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.99-4007G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934152 | |||||||
chr1:53934586 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99-4441G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934586 | |||||||
chr1:53934615 | T | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-4470A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934615 | |||||||
chr1:53934626 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.99-4481A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934626 | |||||||
chr1:53934668 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.99-4523A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934668 | |||||||
chr1:53934671 | G | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-4526C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934671 | |||||||
chr1:53934915 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.99-4770G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934915 | |||||||
chr1:53934954 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0027 others(23): Show |
37 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.99-4809C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53934954 | |||||||
chr1:53935001 | A | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0121 others(10): Show |
16 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.99-4856T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935001 | |||||||
chr1:53935027 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-4882G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935027 | |||||||
chr1:53935104 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98+4881T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935104 | |||||||
chr1:53935106 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+4879C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935106 | |||||||
chr1:53935124 | G | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4861C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935124 | |||||||
chr1:53935206 | G | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4779C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935206 | |||||||
chr1:53935283 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+4702C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935283 | |||||||
chr1:53935450 | T | TGTGTGGG others(2154): Show |
1 | a0001c0001t0002g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2161): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | |||||||
chr1:53935450 | T | TGTGTGGG others(2153): Show |
1 | a0001c0001t0002g0153 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2160): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | |||||||
chr1:53935450 | T | TGTGTGGG others(2153): Show |
1 | a0001c0001t0002g0032 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.98+4534_98+4535ins others(2160): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | |||||||
chr1:53935450 | T | TGTGTGGG others(2154): Show |
1 | a0001c0001t0002g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98+4534_98+4535ins others(2161): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935450 | |||||||
chr1:53935481 | C | T | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+4504G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935481 | |||||||
chr1:53935534 | G | GCCACTGA others(309): Show |
4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+4450_98+4451ins others(316): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935534 | |||||||
chr1:53935602 | A | AC | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0002g0153 |
3 | HG01109.hp1 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.98+4382dupG | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935602 | |||||||
chr1:53935606 | A | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+4379T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935606 | |||||||
chr1:53935630 | C | CT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(6): Show |
14 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+4354dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935630 | |||||||
chr1:53935630 | CT | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0121 others(16): Show |
22 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+4354delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935630 | |||||||
chr1:53935653 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.98+4332T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935653 | |||||||
chr1:53935905 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+4080A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53935905 | |||||||
chr1:53936049 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3936G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936049 | |||||||
chr1:53936095 | T | TA | 6 | a0001c0001t0001g0120 a0001c0001t0001g0132 a0001c0001t0002g0032 others(3): Show |
7 | HG01109.hp1 HG02055.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+3889dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936095 | |||||||
chr1:53936157 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(6): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.98+3828C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936157 | |||||||
chr1:53936224 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.98+3761C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936224 | |||||||
chr1:53936295 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.98+3690G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936295 | |||||||
chr1:53936441 | C | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.98+3544G>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936441 | |||||||
chr1:53936532 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.98+3453C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936532 | |||||||
chr1:53936597 | C | G | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+3388G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936597 | |||||||
chr1:53936642 | A | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0069 |
6 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+3343T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936642 | |||||||
chr1:53936730 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+3255G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936730 | |||||||
chr1:53936773 | TTTGC | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3208_98+3211del others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936773 | |||||||
chr1:53936884 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(3): Show |
12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.98+3101C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53936884 | |||||||
chr1:53937171 | G | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+2814C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937171 | |||||||
chr1:53937244 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.98+2741C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937244 | |||||||
chr1:53937341 | ACTT | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.98+2641_98+2643del others(3): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937341 | |||||||
chr1:53937493 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.98+2492C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937493 | |||||||
chr1:53937778 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+2207A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937778 | |||||||
chr1:53937784 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.98+2201C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937784 | |||||||
chr1:53937791 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+2194T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937791 | |||||||
chr1:53937889 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG00673.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.98+2096A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53937889 | |||||||
chr1:53938008 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98+1977G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938008 | |||||||
chr1:53938022 | C | G | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+1963G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938022 | |||||||
chr1:53938313 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+1672A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938313 | |||||||
chr1:53938360 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.98+1625T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938360 | |||||||
chr1:53938375 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0132 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98+1610T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938375 | |||||||
chr1:53938633 | T | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(6): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.98+1352A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938633 | |||||||
chr1:53938638 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+1347G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938638 | |||||||
chr1:53938683 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1302C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938683 | |||||||
chr1:53938813 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1172C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938813 | |||||||
chr1:53938849 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
77 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.98+1136G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938849 | |||||||
chr1:53938873 | G | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1112C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938873 | |||||||
chr1:53938976 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.98+1009T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938976 | |||||||
chr1:53938992 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.98+993A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53938992 | |||||||
chr1:53939035 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+950A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939035 | |||||||
chr1:53939074 | C | CA | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.98+910dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | |||||||
chr1:53939074 | C | CAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0091 others(8): Show |
14 | HG02055.hp1 HG02074.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+909_98+910dupTT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | |||||||
chr1:53939074 | CA | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0048 others(11): Show |
14 | HG01070.hp2 HG01257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+910delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | |||||||
chr1:53939074 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+900_98+910delTT others(9): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939074 | |||||||
chr1:53939167 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.98+818C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939167 | |||||||
chr1:53939219 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+766T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939219 | |||||||
chr1:53939288 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+697C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939288 | |||||||
chr1:53939321 | T | G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+664A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939321 | |||||||
chr1:53939369 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+616A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939369 | |||||||
chr1:53939390 | C | CA | 13 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(10): Show |
14 | HG01109.hp1 HG02145.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+594dupT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939390 | |||||||
chr1:53939390 | CA | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0057 others(5): Show |
12 | HG01169.hp2 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.98+594delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939390 | |||||||
chr1:53939536 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+449C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939536 | |||||||
chr1:53939540 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.98+445T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939540 | |||||||
chr1:53939676 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+309G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939676 | |||||||
chr1:53939888 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.98+97G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939888 | |||||||
chr1:53939953 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.98+32C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939953 | |||||||
chr1:53939954 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0125 others(1): Show |
6 | HG00639.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+31T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939954 | |||||||
chr1:53939976 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.98+9T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939976 | |||||||
chr1:53939979 | T | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01884.hp2 HG02559.hp2 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.98+6A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 2/5 | chr1 | 53939979 | |||||||
chr1:53940167 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15-70T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940167 | |||||||
chr1:53940346 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-15-249T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940346 | |||||||
chr1:53940383 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-15-286C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940383 | |||||||
chr1:53940413 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15-316G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940413 | |||||||
chr1:53940421 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-324A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940421 | |||||||
chr1:53940447 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15-350T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940447 | |||||||
chr1:53940476 | A | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-379T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940476 | |||||||
chr1:53940694 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-597T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940694 | |||||||
chr1:53940840 | G | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-743C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940840 | |||||||
chr1:53940891 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-794G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940891 | |||||||
chr1:53940895 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-798T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940895 | |||||||
chr1:53940954 | A | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-857T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | |||||||
chr1:53940954 | AT | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-858delA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | |||||||
chr1:53940954 | ATT | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(4): Show |
19 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-859_-15-858del others(2): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53940954 | |||||||
chr1:53941064 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-967C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941064 | |||||||
chr1:53941087 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0001g0102 |
4 | HG01257.hp1 HG01515.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-990G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941087 | |||||||
chr1:53941151 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
8 | HG00423.hp2 HG00438.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1054G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941151 | |||||||
chr1:53941169 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15-1072T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941169 | |||||||
chr1:53941204 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15-1107A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941204 | |||||||
chr1:53941278 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0021 others(7): Show |
16 | HG00408.hp2 HG02040.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1181G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941278 | |||||||
chr1:53941283 | G | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1186C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941283 | |||||||
chr1:53941327 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-15-1230A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941327 | |||||||
chr1:53941386 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1289C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941386 | |||||||
chr1:53941405 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0099 |
3 | HG01496.hp1 HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-15-1308A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941405 | |||||||
chr1:53941430 | T | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-1333A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941430 | |||||||
chr1:53941848 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-15-1751G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941848 | |||||||
chr1:53941890 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0111 a0001c0001t0001g0112 |
6 | HG02572.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-1793G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941890 | |||||||
chr1:53941938 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-1841A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53941938 | |||||||
chr1:53942106 | G | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-2009C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942106 | |||||||
chr1:53942191 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-15-2094A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942191 | |||||||
chr1:53942225 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2128T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942225 | |||||||
chr1:53942436 | G | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2339C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942436 | |||||||
chr1:53942469 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2372G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942469 | |||||||
chr1:53942606 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01257.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-15-2509A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942606 | |||||||
chr1:53942633 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-2536A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942633 | |||||||
chr1:53942752 | T | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2655A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942752 | |||||||
chr1:53942769 | A | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-2672T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942769 | |||||||
chr1:53942878 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
6 | HG00099.hp1 HG01070.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2677G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942878 | |||||||
chr1:53942892 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-16+2663T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942892 | |||||||
chr1:53942912 | C | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
109 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-16+2643G>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942912 | |||||||
chr1:53942962 | A | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+2593T>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53942962 | |||||||
chr1:53943021 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+2534G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943021 | |||||||
chr1:53943076 | C | CT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0113 others(6): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+2478dupA | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943076 | |||||||
chr1:53943164 | T | G | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2391A>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943164 | |||||||
chr1:53943207 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0111 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+2348T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943207 | |||||||
chr1:53943245 | G | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+2310C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943245 | |||||||
chr1:53943275 | A | G | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+2280T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943275 | |||||||
chr1:53943415 | G | GGT | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+2138_-16+2139d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943415 | |||||||
chr1:53943482 | G | GGA | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-16+2071_-16+2072d others(4): Show |
IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943482 | |||||||
chr1:53943511 | G | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+2044C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943511 | |||||||
chr1:53943593 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-16+1962C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943593 | |||||||
chr1:53943620 | G | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+1935C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943620 | |||||||
chr1:53943882 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-16+1673T>C | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943882 | |||||||
chr1:53943885 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0104 |
7 | HG00544.hp1 HG03490.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+1670C>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943885 | |||||||
chr1:53943981 | G | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1574C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53943981 | |||||||
chr1:53944138 | T | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+1417A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944138 | |||||||
chr1:53944279 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
9 | HG01891.hp1 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+1276C>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944279 | |||||||
chr1:53944344 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
38 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+1211A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944344 | |||||||
chr1:53944415 | CA | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1139delT | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944415 | |||||||
chr1:53944517 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-16+1038A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944517 | |||||||
chr1:53944787 | T | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
11 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+768A>T | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944787 | |||||||
chr1:53944938 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-16+617G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944938 | |||||||
chr1:53944982 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(15): Show |
39 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+573A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53944982 | |||||||
chr1:53945057 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-16+498C>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945057 | |||||||
chr1:53945066 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-16+489T>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945066 | |||||||
chr1:53945176 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-16+379A>G | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945176 | |||||||
chr1:53945240 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-16+315G>A | IFT25 | ENSG00000081870.12 | transcript | ENST00000194214.10 | protein_coding | 1/5 | chr1 | 53945240 |