Item | Value |
---|---|
geneid | 112752 |
ensemblid | ENSG00000119650.13 |
hgncid | 29669 |
symbol | IFT43 |
name | intraflagellar transport 43 |
refseq_nuc | NM_001102564.3 |
refseq_prot | NP_001096034.1 |
ensembl_nuc | ENST00000314067.11 |
ensembl_prot | ENSP00000324177.6 |
mane_status | MANE Select |
chr | chr14 |
start | 75985763 |
end | 76083742 |
strand | + |
ver | v1.2 |
region | chr14:75985763-76083742 |
region5000 | chr14:75980763-76088742 |
regionname0 | IFT43_chr14_75985763_76083742 |
regionname5000 | IFT43_chr14_75980763_76088742 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 208 | 392 | 92 | 76 | 168 | 12 | 42 | 132 | IFT43_chr14_75980763_76088742 | IFT43 | MEDLL others(203): Show |
chr14 | 75980763 | 76088742 |
a0002 | 0/0 | 208 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | MEDLL others(203): Show |
chr14 | 75980763 | 76088742 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 624 | 388 | 92 | 76 | 165 | 12 | 41 | IFT43_chr14_75980763_76088742 | IFT43 | ATGGA others(619): Show |
chr14 | 75980763 | 76088742 | ||
a0001c0003 | 0/0 | 624 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | ATGGA others(619): Show |
chr14 | 75980763 | 76088742 | ||
a0001c0004 | 0/0 | 624 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | ATGGA others(619): Show |
chr14 | 75980763 | 76088742 | ||
a0002c0002 | 0/0 | 624 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | ATGGA others(619): Show |
chr14 | 75980763 | 76088742 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 816 | 388 | 92 | 76 | 165 | 12 | 41 | IFT43_chr14_75980763_76088742 | IFT43 | AAGTG others(811): Show |
chr14 | 75980763 | 76088742 |
a0001c0003t0001 | 0/0 | 816 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | AAGTG others(811): Show |
chr14 | 75980763 | 76088742 |
a0001c0004t0001 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | AAGTG others(811): Show |
chr14 | 75980763 | 76088742 |
a0002c0002t0001 | 0/0 | 816 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | AAGTG others(811): Show |
chr14 | 75980763 | 76088742 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0031 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CDX | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0235 | SAS | PJL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ASW | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | GIH | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | GIH | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0305 | REF | REF | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0031 | REF | REF | IFT43_chr14_75980763_76088742 | IFT43 | chr14 | 75980763 | 76088742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:76059332 | G | A | 1 | a0002 | 4 | HG02056.hp2 HG02155.hp2 NA18995.hp1 others(1): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/9 | 278/816 | 254/627 | 85/208 | chr14 | 76059332 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:76083250 | C | T | 1 | a0001c0004 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.468C>T | p.Leu156Leu | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/9 | 492/816 | 468/627 | 156/208 | chr14 | 76083250 | |||
chr14:76083268 | G | A | 1 | a0001c0003 | 3 | HG00423.hp1 HG00609.hp1 HG02155.hp1 |
synonymous_variant | LOW | c.486G>A | p.Ala162Ala | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/9 | 510/816 | 486/627 | 162/208 | chr14 | 76083268 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:75985968 | A | G | 1 | a0001c0001t0001g0350 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54+128A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75985968 | |||||||
chr14:75986137 | C | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
6 | HG02040.hp2 HG02135.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+297C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986137 | |||||||
chr14:75986166 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+326G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986166 | |||||||
chr14:75986172 | A | G | 6 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
7 | HG02630.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+332A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986172 | |||||||
chr14:75986184 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.54+344G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986184 | |||||||
chr14:75986269 | T | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.54+429T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986269 | |||||||
chr14:75986410 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.54+570T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986410 | |||||||
chr14:75986446 | C | CA | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.54+622dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986446 | ||||||
chr14:75986446 | C | CAA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
43 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.54+621_54+622dupAA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986446 | ||||||
chr14:75986537 | A | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+697A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986537 | |||||||
chr14:75986540 | C | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+700C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986540 | |||||||
chr14:75986542 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+702A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986542 | |||||||
chr14:75986548 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0256 others(2): Show |
8 | HG00408.hp2 HG00673.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+708C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986548 | |||||||
chr14:75986549 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.54+709A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986549 | |||||||
chr14:75986567 | A | C | 1 | a0001c0001t0001g0341 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.54+727A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986567 | |||||||
chr14:75986629 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+789C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986629 | |||||||
chr14:75986753 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+913G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986753 | |||||||
chr14:75986754 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.54+914C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986754 | |||||||
chr14:75986809 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+969C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986809 | |||||||
chr14:75986841 | T | TA | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1002dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75986841 | ||||||
chr14:75986844 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+1004G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986844 | |||||||
chr14:75986939 | G | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+1099G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75986939 | |||||||
chr14:75987038 | A | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.54+1198A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987038 | |||||||
chr14:75987071 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.54+1231C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987071 | |||||||
chr14:75987110 | C | G | 1 | a0001c0001t0001g0340 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.54+1270C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987110 | |||||||
chr14:75987252 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.54+1412A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987252 | |||||||
chr14:75987460 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55-1425G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987460 | |||||||
chr14:75987555 | A | G | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-1330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987555 | |||||||
chr14:75987776 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.55-1109C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987776 | |||||||
chr14:75987815 | AATTTTGA others(3): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.55-1069_55-1060del others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75987815 | |||||||
chr14:75988085 | C | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-800C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988085 | |||||||
chr14:75988176 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-709T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988176 | |||||||
chr14:75988343 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(34): Show |
43 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.55-542C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988343 | |||||||
chr14:75988517 | CT | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.55-359delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 75988517 | ||||||
chr14:75988536 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.55-349T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988536 | |||||||
chr14:75988868 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.55-17T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 1/8 | chr14 | 75988868 | |||||||
chr14:75989011 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.147+34T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989011 | |||||||
chr14:75989024 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+47T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989024 | |||||||
chr14:75989038 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.147+61A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989038 | |||||||
chr14:75989066 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+89C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989066 | |||||||
chr14:75989090 | T | C | 1 | a0001c0001t0001g0012 | 2 | NA18953.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.147+113T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989090 | |||||||
chr14:75989146 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+169G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989146 | |||||||
chr14:75989385 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+408A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989385 | |||||||
chr14:75989586 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.147+609C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989586 | |||||||
chr14:75989798 | C | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+821C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75989798 | |||||||
chr14:75990185 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1208G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990185 | |||||||
chr14:75990280 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1303G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990280 | |||||||
chr14:75990411 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.147+1434A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990411 | |||||||
chr14:75990511 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.147+1534T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990511 | |||||||
chr14:75990625 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+1648G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990625 | |||||||
chr14:75990642 | C | T | 3 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0255 |
3 | HG02647.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.147+1665C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990642 | |||||||
chr14:75990678 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+1701G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990678 | |||||||
chr14:75990710 | A | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+1733A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75990710 | |||||||
chr14:75991171 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.147+2194T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991171 | |||||||
chr14:75991262 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2285C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991262 | |||||||
chr14:75991359 | T | TTA | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+2397_147+2398d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | ||||||
chr14:75991359 | T | TTATA | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+2395_147+2398d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | ||||||
chr14:75991359 | TTA | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0345 a0002c0002t0001g0304 |
4 | HG02155.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+2397_147+2398d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991359 | ||||||
chr14:75991388 | A | AGT | 14 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0074 others(11): Show |
16 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.147+2448_147+2449d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | A | AGTGT | 8 | a0001c0001t0001g0121 a0001c0001t0001g0242 a0001c0001t0001g0300 others(5): Show |
9 | HG02027.hp2 HG02155.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+2446_147+2449d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | A | AGTGTGT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0301 a0001c0001t0001g0335 others(2): Show |
8 | HG02056.hp2 HG03017.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+2444_147+2449d others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | A | AGTGTGTG others(19): Show |
1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+2423_147+2424i others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | A | AGTGTGTG others(23): Show |
1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+2423_147+2424i others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGT | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.147+2448_147+2449d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGTGT | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0035 others(27): Show |
33 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.147+2446_147+2449d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGTGTGT | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(93): Show |
109 | HG00609.hp2 HG00673.hp1 HG00741.hp1 others(106): Show |
intron_variant | MODIFIER | c.147+2444_147+2449d others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGTGTGTG others(1): Show |
A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0081 a0001c0001t0001g0082 others(6): Show |
10 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.147+2442_147+2449d others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0141 a0001c0001t0001g0142 |
4 | HG00735.hp1 HG02148.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2440_147+2449d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991388 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18985.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.147+2438_147+2449d others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991388 | ||||||
chr14:75991390 | T | TGTGTGTG others(15): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0039 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991390 | ||||||
chr14:75991392 | T | TGTGTGTG others(13): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991392 | ||||||
chr14:75991394 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.147+2417T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991394 | |||||||
chr14:75991394 | T | TGTGTGTA others(11): Show |
4 | a0001c0001t0001g0118 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991394 | ||||||
chr14:75991396 | T | TGTGTATA others(9): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+2423_147+2424i others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991396 | ||||||
chr14:75991423 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0212 |
2 | HG01192.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.147+2446G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991423 | |||||||
chr14:75991423 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00280.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+2449_147+2450i others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75991423 | ||||||
chr14:75991427 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
5 | HG02723.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+2450A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991427 | |||||||
chr14:75991433 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00280.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.147+2456G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991433 | |||||||
chr14:75991516 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+2539C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991516 | |||||||
chr14:75991738 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+2761A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991738 | |||||||
chr14:75991883 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(17): Show |
29 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.147+2906C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75991883 | |||||||
chr14:75992008 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+3031C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992008 | |||||||
chr14:75992049 | C | T | 1 | a0001c0004t0001g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147+3072C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992049 | |||||||
chr14:75992050 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.147+3073G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992050 | |||||||
chr14:75992123 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.147+3146A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992123 | |||||||
chr14:75992242 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.147+3265A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992242 | |||||||
chr14:75992304 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+3327T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992304 | |||||||
chr14:75992307 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+3330G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992307 | |||||||
chr14:75992321 | C | T | 2 | a0001c0001t0001g0241 a0001c0004t0001g0235 |
2 | HG01934.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.147+3344C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992321 | |||||||
chr14:75992497 | ACTC | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.147+3521_147+3523d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992497 | |||||||
chr14:75992525 | G | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(7): Show |
12 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+3548G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992525 | |||||||
chr14:75992589 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.147+3612A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992589 | |||||||
chr14:75992593 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+3616T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992593 | |||||||
chr14:75992649 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.147+3672G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992649 | |||||||
chr14:75992878 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.147+3901G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75992878 | |||||||
chr14:75993027 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
37 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.147+4050A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993027 | |||||||
chr14:75993085 | T | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4108T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993085 | |||||||
chr14:75993146 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147+4169A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993146 | |||||||
chr14:75993199 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.147+4222G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993199 | |||||||
chr14:75993229 | G | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4252G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993229 | |||||||
chr14:75993387 | T | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4410T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993387 | |||||||
chr14:75993530 | A | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+4553A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993530 | |||||||
chr14:75993535 | A | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+4558A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993535 | |||||||
chr14:75993680 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+4703C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993680 | |||||||
chr14:75993817 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+4840G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993817 | |||||||
chr14:75993997 | C | G | 1 | a0001c0001t0001g0350 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.147+5020C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75993997 | |||||||
chr14:75994032 | T | G | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5055T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994032 | |||||||
chr14:75994103 | C | CT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0040 others(8): Show |
14 | HG00597.hp1 HG01074.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.147+5138dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75994103 | ||||||
chr14:75994103 | C | CTT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+5137_147+5138d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75994103 | ||||||
chr14:75994161 | G | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5184G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994161 | |||||||
chr14:75994182 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.147+5205G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994182 | |||||||
chr14:75994185 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+5208T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994185 | |||||||
chr14:75994279 | C | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
11 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+5302C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994279 | |||||||
chr14:75994291 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.147+5314G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994291 | |||||||
chr14:75994403 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.147+5426C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994403 | |||||||
chr14:75994454 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.147+5477A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994454 | |||||||
chr14:75994546 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.147+5569C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994546 | |||||||
chr14:75994625 | G | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+5648G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994625 | |||||||
chr14:75994638 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+5661C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994638 | |||||||
chr14:75994779 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+5802G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75994779 | |||||||
chr14:75995087 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.147+6110A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995087 | |||||||
chr14:75995107 | T | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0118 others(8): Show |
11 | HG01123.hp2 HG01361.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+6130T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995107 | |||||||
chr14:75995154 | G | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+6177G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995154 | |||||||
chr14:75995189 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0255 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.147+6212A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995189 | |||||||
chr14:75995433 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+6456C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995433 | |||||||
chr14:75995491 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
47 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.147+6514C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995491 | |||||||
chr14:75995619 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG02027.hp1 NA18972.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.147+6642C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995619 | |||||||
chr14:75995683 | T | G | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.147+6706T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995683 | |||||||
chr14:75995759 | C | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+6782C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995759 | |||||||
chr14:75995904 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+6927C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995904 | |||||||
chr14:75995926 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.147+6949C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995926 | |||||||
chr14:75995954 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+6977G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75995954 | |||||||
chr14:75996046 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147+7069T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996046 | |||||||
chr14:75996142 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.147+7165C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996142 | |||||||
chr14:75996174 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+7197T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996174 | |||||||
chr14:75996253 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.147+7276C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996253 | |||||||
chr14:75996392 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.147+7415A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996392 | |||||||
chr14:75996451 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.147+7474T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996451 | |||||||
chr14:75996524 | T | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(92): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.147+7547T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996524 | |||||||
chr14:75996758 | T | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.147+7781T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996758 | |||||||
chr14:75996991 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.147+8014G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75996991 | |||||||
chr14:75997152 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.147+8175A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997152 | |||||||
chr14:75997175 | GAC | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+8200_147+8201d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75997175 | ||||||
chr14:75997179 | A | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+8202A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997179 | |||||||
chr14:75997211 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8234T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997211 | |||||||
chr14:75997334 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8357C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997334 | |||||||
chr14:75997357 | A | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0045 others(11): Show |
16 | HG00597.hp2 HG00609.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.147+8380A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997357 | |||||||
chr14:75997851 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+8874T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997851 | |||||||
chr14:75997884 | T | TTGTAAAA others(3): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+8912_147+8921d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75997884 | ||||||
chr14:75997943 | T | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+8966T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997943 | |||||||
chr14:75997972 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+8995C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75997972 | |||||||
chr14:75998135 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.147+9158G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998135 | |||||||
chr14:75998211 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.147+9234C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998211 | |||||||
chr14:75998220 | T | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(92): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.147+9243T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998220 | |||||||
chr14:75998299 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+9322G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998299 | |||||||
chr14:75998488 | T | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(154): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.147+9511T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998488 | |||||||
chr14:75998489 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+9512G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998489 | |||||||
chr14:75998522 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(11): Show |
16 | HG01109.hp2 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.147+9545G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998522 | |||||||
chr14:75998648 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.147+9671A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998648 | |||||||
chr14:75998702 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.147+9725G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998702 | |||||||
chr14:75998827 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0263 |
2 | HG01167.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.147+9850G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998827 | |||||||
chr14:75998944 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+9967G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998944 | |||||||
chr14:75998988 | G | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(2): Show |
5 | HG00438.hp2 HG02071.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10011G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75998988 | |||||||
chr14:75999037 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
46 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.147+10060G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999037 | |||||||
chr14:75999089 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(1): Show |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10112T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999089 | |||||||
chr14:75999120 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10143G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999120 | |||||||
chr14:75999186 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10209C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999186 | |||||||
chr14:75999225 | TTTTATAT others(3): Show |
T | 1 | a0001c0001t0001g0108 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.147+10250_147+1025 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999225 | ||||||
chr14:75999226 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+10249T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999226 | |||||||
chr14:75999226 | T | TTATATAT others(30): Show |
1 | a0001c0001t0001g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+10250_147+1025 others(41): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999226 | ||||||
chr14:75999227 | T | TATATATA others(36): Show |
1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.147+10250_147+1025 others(47): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999227 | |||||||
chr14:75999227 | TTA | T | 12 | a0001c0001t0001g0289 a0001c0001t0001g0292 a0001c0001t0001g0314 others(9): Show |
12 | HG00408.hp1 HG00673.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10294_147+1029 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | ||||||
chr14:75999227 | TTATA | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0042 others(4): Show |
7 | HG00597.hp1 HG02109.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+10292_147+1029 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | ||||||
chr14:75999227 | TTATATA | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0317 a0001c0001t0001g0336 |
3 | NA18986.hp1 NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.147+10290_147+1029 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | ||||||
chr14:75999227 | TTATATAT others(13): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+10276_147+1029 others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999227 | ||||||
chr14:75999229 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999229 | ||||||
chr14:75999229 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+10252A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999229 | |||||||
chr14:75999230 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.147+10253T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999230 | |||||||
chr14:75999231 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.147+10262_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999231 | ||||||
chr14:75999231 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(40): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999231 | ||||||
chr14:75999233 | A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0060 a0001c0001t0001g0062 others(1): Show |
4 | HG01081.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999233 | ||||||
chr14:75999235 | A | ATATATAA others(25): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0070 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(36): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999235 | ||||||
chr14:75999235 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.147+10266_147+1026 others(38): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999235 | ||||||
chr14:75999237 | A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.147+10264_147+1026 others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | ||||||
chr14:75999237 | A | ATATAATA others(23): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
7 | HG01074.hp1 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | ||||||
chr14:75999237 | A | ATATATAA others(25): Show |
3 | a0001c0001t0001g0115 a0001c0001t0001g0220 a0001c0001t0001g0279 |
3 | HG01358.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(36): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999237 | ||||||
chr14:75999239 | A | ATAATATT others(4): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0071 |
2 | HG02015.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | ||||||
chr14:75999239 | A | ATAATATT others(21): Show |
1 | a0001c0001t0001g0048 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.147+10264_147+1026 others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | ||||||
chr14:75999239 | A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0229 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.147+10266_147+1026 others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | ||||||
chr14:75999239 | A | ATATAATA others(23): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02004.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999239 | ||||||
chr14:75999241 | A | AATATTCA others(2): Show |
6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | HG01175.hp1 HG01928.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | |||||||
chr14:75999241 | A | AATATTCA others(17): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10264_147+1026 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | |||||||
chr14:75999241 | A | AATATTCA others(19): Show |
2 | a0001c0001t0001g0049 a0001c0001t0001g0073 |
2 | HG02818.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.147+10264_147+1026 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999241 | |||||||
chr14:75999241 | A | ATAATATT others(4): Show |
12 | a0001c0001t0001g0041 a0001c0001t0001g0204 a0001c0001t0001g0230 others(9): Show |
12 | HG01517.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999241 | ||||||
chr14:75999241 | A | ATAATATT others(21): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG00280.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.147+10266_147+1026 others(32): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999241 | ||||||
chr14:75999243 | A | AATATTCA others(2): Show |
32 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(29): Show |
37 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | |||||||
chr14:75999243 | A | AATATTCA others(17): Show |
11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG00099.hp2 HG01934.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | |||||||
chr14:75999243 | A | AATATTCA others(19): Show |
8 | a0001c0001t0001g0141 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
8 | HG00423.hp2 HG00733.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+10266_147+1026 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | |||||||
chr14:75999243 | A | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10266A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999243 | |||||||
chr14:75999243 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.147+10268_147+1030 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999243 | ||||||
chr14:75999245 | A | T | 12 | a0001c0001t0001g0065 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
12 | HG00099.hp2 HG01934.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.147+10268A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999245 | |||||||
chr14:75999245 | ATATATAT others(32): Show |
A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0125 others(27): Show |
32 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.147+10270_147+1030 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999245 | ||||||
chr14:75999245 | ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA19056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.147+10270_147+1030 others(44): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999245 | ||||||
chr14:75999246 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.147+10269T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999246 | |||||||
chr14:75999247 | A | AAATTCAT others(2): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0071 a0001c0001t0001g0229 |
3 | HG02015.hp1 HG02165.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.147+10270_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999247 | |||||||
chr14:75999247 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.147+10270A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999247 | |||||||
chr14:75999247 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.147+10280_147+1030 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | ||||||
chr14:75999247 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.147+10272_147+1030 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | ||||||
chr14:75999247 | ATATATAT others(32): Show |
A | 49 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
51 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.147+10272_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | ||||||
chr14:75999247 | ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0140 |
2 | HG01496.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.147+10272_147+1031 others(44): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999247 | ||||||
chr14:75999248 | TATATATA others(16): Show |
T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
4 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10272_147+1029 others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999248 | |||||||
chr14:75999249 | A | AAATTCAT others(2): Show |
17 | a0001c0001t0001g0041 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
17 | HG01175.hp1 HG01517.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.147+10272_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | |||||||
chr14:75999249 | A | AAATTCAT others(4): Show |
1 | a0001c0001t0001g0265 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.147+10272_147+1027 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | |||||||
chr14:75999249 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0282 others(2): Show |
12 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.147+10272A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | |||||||
chr14:75999249 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.147+10272A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999249 | |||||||
chr14:75999249 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.147+10282_147+1030 others(28): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | ||||||
chr14:75999249 | ATATATAT others(31): Show |
A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0208 |
3 | HG02027.hp1 NA18967.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.147+10274_147+1031 others(42): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | ||||||
chr14:75999249 | ATATATAT others(32): Show |
A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0132 a0001c0001t0001g0135 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10274_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999249 | ||||||
chr14:75999250 | TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.147+10274_147+1029 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999250 | |||||||
chr14:75999251 | A | AAATTCAT others(2): Show |
30 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(27): Show |
35 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.147+10274_147+1027 others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999251 | |||||||
chr14:75999251 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.147+10284_147+1030 others(26): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999251 | ||||||
chr14:75999251 | ATATATAT others(32): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.147+10276_147+1031 others(43): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999251 | ||||||
chr14:75999252 | TATATATA others(16): Show |
T | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.147+10276_147+1029 others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999252 | |||||||
chr14:75999253 | A | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0285 |
2 | HG00438.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.147+10276A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999253 | |||||||
chr14:75999253 | ATATATAT others(13): Show |
A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0252 others(2): Show |
6 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10286_147+1030 others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999253 | ||||||
chr14:75999253 | ATATATAT others(24): Show |
A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+10278_147+1030 others(35): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999253 | ||||||
chr14:75999255 | ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0101 others(3): Show |
6 | HG02572.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10288_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999255 | ||||||
chr14:75999256 | TATATATA others(14): Show |
T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+10280_147+1030 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999256 | |||||||
chr14:75999257 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.147+10280A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999257 | |||||||
chr14:75999257 | ATATATAT others(18): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0282 others(2): Show |
11 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+10282_147+1030 others(29): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999257 | ||||||
chr14:75999257 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0002 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.147+10282_147+1030 others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999257 | ||||||
chr14:75999259 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0088 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147+10292_147+1030 others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | ||||||
chr14:75999259 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0350 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.147+10284_147+1030 others(29): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | ||||||
chr14:75999259 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.147+10284_147+1031 others(34): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999259 | ||||||
chr14:75999260 | TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.147+10284_147+1030 others(25): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999260 | |||||||
chr14:75999261 | ATATATAT others(5): Show |
A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0076 others(3): Show |
6 | HG01361.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+10294_147+1030 others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999261 | ||||||
chr14:75999262 | TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.147+10286_147+1030 others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999262 | |||||||
chr14:75999263 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.147+10286A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999263 | |||||||
chr14:75999263 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0249 a0001c0001t0001g0306 |
3 | HG02717.hp1 HG02735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.147+10296_147+1030 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999263 | ||||||
chr14:75999263 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.147+10288_147+1030 others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999263 | ||||||
chr14:75999264 | TATATATA others(8): Show |
T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0072 |
2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.147+10288_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999264 | |||||||
chr14:75999265 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.147+10288A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999265 | |||||||
chr14:75999265 | ATATATAT others(1): Show |
A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0087 others(5): Show |
8 | HG01175.hp2 HG01981.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+10296_147+1030 others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | ||||||
chr14:75999265 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(21): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | ||||||
chr14:75999265 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999265 | ||||||
chr14:75999266 | TATATATG others(8): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.147+10290_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999266 | |||||||
chr14:75999267 | ATATATG | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0091 others(3): Show |
6 | HG00597.hp2 HG00733.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+10296_147+1030 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | ||||||
chr14:75999267 | ATATATGT others(8): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(19): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | ||||||
chr14:75999267 | ATATATGT others(11): Show |
A | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999267 | ||||||
chr14:75999268 | TATATGTA others(4): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147+10292_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999268 | |||||||
chr14:75999269 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0322 |
3 | HG03831.hp2 NA18522.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.147+10292A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999269 | |||||||
chr14:75999269 | ATATG | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+10296_147+1029 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999269 | ||||||
chr14:75999270 | TATGTATA others(4): Show |
T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.147+10294_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999270 | |||||||
chr14:75999271 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.147+10294A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999271 | |||||||
chr14:75999271 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.147+10294A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999271 | |||||||
chr14:75999271 | ATG | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0045 others(2): Show |
5 | HG00609.hp2 HG03834.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+10296_147+1029 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999271 | ||||||
chr14:75999271 | ATGTATAT others(4): Show |
A | 1 | a0001c0001t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.147+10296_147+1030 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999271 | ||||||
chr14:75999273 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(135): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.147+10296G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999273 | |||||||
chr14:75999273 | G | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(5): Show |
8 | HG01109.hp2 HG02135.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+10296G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999273 | |||||||
chr14:75999274 | TATATATA | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0093 |
3 | HG00099.hp1 HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.147+10298_147+1030 others(11): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999274 | |||||||
chr14:75999275 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0291 others(1): Show |
5 | NA18950.hp1 NA18978.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+10298A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999275 | |||||||
chr14:75999275 | A | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
11 | HG01109.hp2 HG02135.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.147+10298A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999275 | |||||||
chr14:75999275 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.147+10300_147+1031 others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999275 | ||||||
chr14:75999275 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.147+10300_147+1031 others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999275 | ||||||
chr14:75999277 | A | ATTT | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0066 |
3 | HG01175.hp1 HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.147+10301_147+1030 others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999277 | ||||||
chr14:75999277 | A | G | 4 | a0001c0001t0001g0311 a0001c0001t0001g0318 a0001c0001t0001g0321 others(1): Show |
4 | NA18998.hp1 NA19057.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10300A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999277 | |||||||
chr14:75999277 | A | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0034 others(22): Show |
27 | HG01106.hp1 HG01109.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.147+10300A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999277 | |||||||
chr14:75999278 | TA | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0270 a0001c0001t0001g0278 |
3 | HG01884.hp1 HG03927.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.147+10302delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999278 | |||||||
chr14:75999279 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0290 a0002c0002t0001g0337 |
3 | HG02056.hp2 NA18612.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.147+10302A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999279 | |||||||
chr14:75999279 | A | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(42): Show |
48 | HG00597.hp2 HG01106.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.147+10302A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999279 | |||||||
chr14:75999280 | TA | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
8 | HG01934.hp2 HG03139.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+10304delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999280 | |||||||
chr14:75999281 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0279 |
2 | HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+10314_147+1032 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999281 | ||||||
chr14:75999281 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.147+10304A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999281 | |||||||
chr14:75999281 | A | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(70): Show |
79 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.147+10304A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999281 | |||||||
chr14:75999281 | AT | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0027 others(40): Show |
47 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.147+10323delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 75999281 | ||||||
chr14:75999282 | T | TA | 8 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0064 others(5): Show |
9 | HG00280.hp2 HG02698.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+10305_147+1030 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | |||||||
chr14:75999282 | T | TATA | 4 | a0001c0001t0001g0311 a0001c0001t0001g0318 a0001c0001t0001g0321 others(1): Show |
4 | NA18998.hp1 NA19057.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+10305_147+1030 others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | |||||||
chr14:75999282 | T | TATATA | 3 | a0001c0001t0001g0028 a0001c0001t0001g0290 a0002c0002t0001g0337 |
3 | HG02056.hp2 NA18612.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.147+10305_147+1030 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999282 | |||||||
chr14:75999283 | T | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(32): Show |
37 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.147+10306T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999283 | |||||||
chr14:75999284 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0335 a0002c0002t0001g0033 |
3 | NA18612.hp1 NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.147+10307T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999284 | |||||||
chr14:75999285 | T | A | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0229 others(6): Show |
9 | HG00642.hp2 HG01081.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+10308T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999285 | |||||||
chr14:75999300 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+10323T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999300 | |||||||
chr14:75999342 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0279 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+10365G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999342 | |||||||
chr14:75999354 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+10377C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999354 | |||||||
chr14:75999427 | A | G | 1 | a0001c0001t0001g0348 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.147+10450A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999427 | |||||||
chr14:75999697 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.147+10720A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999697 | |||||||
chr14:75999802 | G | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+10825G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999802 | |||||||
chr14:75999995 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+11018G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 75999995 | |||||||
chr14:76000044 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.147+11067C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000044 | |||||||
chr14:76000168 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147+11191T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000168 | |||||||
chr14:76000239 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.147+11262T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000239 | |||||||
chr14:76000262 | C | CT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0089 others(4): Show |
8 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+11305dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | ||||||
chr14:76000262 | CT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(104): Show |
116 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(113): Show |
intron_variant | MODIFIER | c.147+11305delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | ||||||
chr14:76000262 | CTTTT | C | 16 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(13): Show |
17 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.147+11302_147+1130 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000262 | ||||||
chr14:76000369 | A | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.147+11392A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000369 | |||||||
chr14:76000392 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.147+11415G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000392 | |||||||
chr14:76000402 | C | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+11425C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000402 | |||||||
chr14:76000421 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+11444C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000421 | |||||||
chr14:76000431 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0022 others(20): Show |
27 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.147+11468dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000431 | ||||||
chr14:76000431 | AT | A | 16 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(13): Show |
17 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.147+11468delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76000431 | ||||||
chr14:76000474 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+11497G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000474 | |||||||
chr14:76000563 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.147+11586C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000563 | |||||||
chr14:76000680 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+11703G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000680 | |||||||
chr14:76000856 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.147+11879C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76000856 | |||||||
chr14:76001013 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+12036C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001013 | |||||||
chr14:76001147 | G | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0122 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+12170G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001147 | |||||||
chr14:76001420 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+12443G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001420 | |||||||
chr14:76001559 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0279 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.147+12582C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001559 | |||||||
chr14:76001634 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+12657G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001634 | |||||||
chr14:76001892 | T | G | 5 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0122 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+12915T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001892 | |||||||
chr14:76001985 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13008T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76001985 | |||||||
chr14:76002222 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.147+13245G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002222 | |||||||
chr14:76002299 | T | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.147+13322T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002299 | |||||||
chr14:76002336 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(35): Show |
43 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.147+13359C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002336 | |||||||
chr14:76002363 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13386G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002363 | |||||||
chr14:76002366 | AG | A | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.147+13398delG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76002366 | ||||||
chr14:76002378 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+13401G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002378 | |||||||
chr14:76002453 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13476G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002453 | |||||||
chr14:76002497 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(33): Show |
41 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.147+13520C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002497 | |||||||
chr14:76002535 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.147+13558C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002535 | |||||||
chr14:76002750 | A | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13773A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002750 | |||||||
chr14:76002751 | T | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+13774T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002751 | |||||||
chr14:76002888 | G | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0122 others(3): Show |
7 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+13911G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002888 | |||||||
chr14:76002964 | C | T | 87 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
93 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.147+13987C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76002964 | |||||||
chr14:76003019 | C | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
188 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.147+14042C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003019 | |||||||
chr14:76003121 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.147+14144G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003121 | |||||||
chr14:76003438 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+14461C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003438 | |||||||
chr14:76003647 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+14670G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003647 | |||||||
chr14:76003696 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.147+14719C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003696 | |||||||
chr14:76003772 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+14795G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76003772 | |||||||
chr14:76004014 | G | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0168 |
3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.147+15037G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004014 | |||||||
chr14:76004020 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.147+15043C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004020 | |||||||
chr14:76004037 | A | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0096 others(1): Show |
4 | HG01993.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+15060A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004037 | |||||||
chr14:76004066 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+15089A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004066 | |||||||
chr14:76004234 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.147+15257A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004234 | |||||||
chr14:76004312 | T | C | 28 | a0001c0001t0001g0141 a0001c0001t0001g0201 a0001c0001t0001g0202 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.147+15335T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004312 | |||||||
chr14:76004336 | G | GT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0122 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.147+15369dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76004336 | ||||||
chr14:76004418 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02451.hp2 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.147+15441G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004418 | |||||||
chr14:76004485 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.147+15508A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004485 | |||||||
chr14:76004580 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+15603A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004580 | |||||||
chr14:76004589 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.147+15612T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76004589 | |||||||
chr14:76005088 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+16111T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005088 | |||||||
chr14:76005128 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02922.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.147+16151A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005128 | |||||||
chr14:76005296 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.147+16319G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005296 | |||||||
chr14:76005325 | G | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.147+16348G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005325 | |||||||
chr14:76005377 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+16400G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005377 | |||||||
chr14:76005477 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.147+16500A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005477 | |||||||
chr14:76005497 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.147+16520T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005497 | |||||||
chr14:76005649 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.147+16672T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005649 | |||||||
chr14:76005742 | T | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-16585T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005742 | |||||||
chr14:76005931 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148-16396C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76005931 | |||||||
chr14:76006061 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.148-16266G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006061 | |||||||
chr14:76006216 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-16111C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006216 | |||||||
chr14:76006225 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-16102G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006225 | |||||||
chr14:76006423 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-15904T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006423 | |||||||
chr14:76006615 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15712C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006615 | |||||||
chr14:76006782 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15545C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006782 | |||||||
chr14:76006838 | T | G | 1 | a0001c0001t0001g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.148-15489T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006838 | |||||||
chr14:76006855 | A | AT | 84 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0025 others(81): Show |
88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.148-15452dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76006855 | ||||||
chr14:76006855 | AT | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0035 others(7): Show |
12 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.148-15452delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76006855 | ||||||
chr14:76006861 | T | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-15466T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006861 | |||||||
chr14:76006930 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-15397C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76006930 | |||||||
chr14:76007034 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0335 |
3 | HG02071.hp1 NA18940.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.148-15293T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007034 | |||||||
chr14:76007048 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-15279G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007048 | |||||||
chr14:76007098 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.148-15229A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007098 | |||||||
chr14:76007115 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.148-15212T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007115 | |||||||
chr14:76007164 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-15163C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007164 | |||||||
chr14:76007339 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.148-14988G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007339 | |||||||
chr14:76007547 | G | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.148-14780G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007547 | |||||||
chr14:76007606 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-14721G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007606 | |||||||
chr14:76007677 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01928.hp1 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.148-14650C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007677 | |||||||
chr14:76007846 | G | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-14481G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007846 | |||||||
chr14:76007872 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-14455G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007872 | |||||||
chr14:76007932 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.148-14395C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76007932 | |||||||
chr14:76008077 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.148-14250A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008077 | |||||||
chr14:76008149 | T | C | 5 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-14178T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008149 | |||||||
chr14:76008425 | T | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(5): Show |
9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-13902T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008425 | |||||||
chr14:76008740 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-13587T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76008740 | |||||||
chr14:76009143 | A | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(48): Show |
60 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.148-13184A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009143 | |||||||
chr14:76009169 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0234 |
3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.148-13158C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009169 | |||||||
chr14:76009345 | G | C | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-12982G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009345 | |||||||
chr14:76009391 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.148-12936A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009391 | |||||||
chr14:76009441 | CT | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-12885delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009441 | |||||||
chr14:76009485 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.148-12842G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009485 | |||||||
chr14:76009606 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-12721A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009606 | |||||||
chr14:76009683 | G | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12644G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009683 | |||||||
chr14:76009768 | C | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12559C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009768 | |||||||
chr14:76009801 | G | GTTTTTTT others(3): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.148-12524_148-1251 others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76009801 | ||||||
chr14:76009801 | GT | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-12515delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76009801 | ||||||
chr14:76009866 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.148-12461C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009866 | |||||||
chr14:76009904 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.148-12423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009904 | |||||||
chr14:76009953 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.148-12374C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009953 | |||||||
chr14:76009978 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(5): Show |
9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-12349A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009978 | |||||||
chr14:76009991 | C | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(155): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.148-12336C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76009991 | |||||||
chr14:76010114 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.148-12213T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010114 | |||||||
chr14:76010340 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
56 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-11987A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010340 | |||||||
chr14:76010387 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(136): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.148-11940C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010387 | |||||||
chr14:76010468 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-11859A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010468 | |||||||
chr14:76010498 | G | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0028 others(26): Show |
33 | HG01167.hp1 HG01243.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.148-11829G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010498 | |||||||
chr14:76010524 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-11803A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010524 | |||||||
chr14:76010643 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0231 a0001c0001t0001g0255 |
3 | HG01167.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.148-11684G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010643 | |||||||
chr14:76010679 | T | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0138 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.148-11648T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010679 | |||||||
chr14:76010803 | G | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0044 others(7): Show |
11 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-11524G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010803 | |||||||
chr14:76010902 | T | TA | 20 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0096 others(17): Show |
21 | HG01891.hp2 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.148-11425_148-1142 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010902 | |||||||
chr14:76010903 | C | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.148-11424C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010903 | |||||||
chr14:76010904 | C | T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0096 others(17): Show |
21 | HG01891.hp2 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.148-11423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010904 | |||||||
chr14:76010904 | CT | C | 10 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0135 others(7): Show |
10 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-11408delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76010904 | ||||||
chr14:76010953 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148-11374A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010953 | |||||||
chr14:76010995 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.148-11332T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76010995 | |||||||
chr14:76011068 | AATTATT | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02486.hp1 HG02723.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.148-11243_148-1123 others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76011068 | ||||||
chr14:76011102 | G | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-11225G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011102 | |||||||
chr14:76011183 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(44): Show |
56 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.148-11144T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011183 | |||||||
chr14:76011360 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10967A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011360 | |||||||
chr14:76011425 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-10902T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011425 | |||||||
chr14:76011442 | C | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10885C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011442 | |||||||
chr14:76011769 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0072 |
3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.148-10558T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011769 | |||||||
chr14:76011770 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-10557A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011770 | |||||||
chr14:76011786 | G | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0306 a0001c0001t0001g0307 |
4 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-10541G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011786 | |||||||
chr14:76011890 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10437C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011890 | |||||||
chr14:76011921 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.148-10406C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76011921 | |||||||
chr14:76012018 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-10309G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012018 | |||||||
chr14:76012024 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.148-10303T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012024 | |||||||
chr14:76012071 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-10256T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012071 | |||||||
chr14:76012148 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.148-10179G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012148 | |||||||
chr14:76012319 | CCATATAA others(10): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-10005_148-9989 others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76012319 | ||||||
chr14:76012382 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0279 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.148-9945T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012382 | |||||||
chr14:76012497 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-9830G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012497 | |||||||
chr14:76012586 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.148-9741G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012586 | |||||||
chr14:76012671 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.148-9656A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012671 | |||||||
chr14:76012713 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-9614A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76012713 | |||||||
chr14:76012763 | CTCTT | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-9558_148-9555d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76012763 | ||||||
chr14:76013018 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-9309G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013018 | |||||||
chr14:76013237 | A | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.148-9090A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013237 | |||||||
chr14:76013398 | A | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-8929A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013398 | |||||||
chr14:76013410 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.148-8917G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013410 | |||||||
chr14:76013415 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0255 |
3 | HG02965.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148-8912C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013415 | |||||||
chr14:76013418 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-8909C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013418 | |||||||
chr14:76013419 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.148-8908G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013419 | |||||||
chr14:76013435 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0088 |
5 | HG02451.hp1 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-8892C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013435 | |||||||
chr14:76013518 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.148-8809A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013518 | |||||||
chr14:76013537 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(5): Show |
9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-8790C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013537 | |||||||
chr14:76013583 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-8744G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76013583 | |||||||
chr14:76013885 | TAAAACAA others(3): Show |
T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-8438_148-8429d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76013885 | ||||||
chr14:76014045 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.148-8282G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014045 | |||||||
chr14:76014102 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-8225A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014102 | |||||||
chr14:76014232 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.148-8095A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014232 | |||||||
chr14:76014341 | C | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7986C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014341 | |||||||
chr14:76014651 | A | AG | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-7676_148-7675i others(3): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014651 | |||||||
chr14:76014720 | T | C | 26 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(23): Show |
26 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.148-7607T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014720 | |||||||
chr14:76014728 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.148-7599G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014728 | |||||||
chr14:76014814 | G | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.148-7513G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014814 | |||||||
chr14:76014840 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-7487G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014840 | |||||||
chr14:76014880 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.148-7447A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014880 | |||||||
chr14:76014941 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148-7386G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76014941 | |||||||
chr14:76015014 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148-7313A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015014 | |||||||
chr14:76015042 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-7285T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015042 | |||||||
chr14:76015062 | C | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7265C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015062 | |||||||
chr14:76015146 | TATTA | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(5): Show |
9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7175_148-7172d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76015146 | ||||||
chr14:76015299 | C | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-7028C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015299 | |||||||
chr14:76015361 | C | T | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-6966C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015361 | |||||||
chr14:76015599 | A | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.148-6728A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015599 | |||||||
chr14:76015804 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-6523T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015804 | |||||||
chr14:76015825 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.148-6502C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015825 | |||||||
chr14:76015826 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-6501G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015826 | |||||||
chr14:76015845 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.148-6482A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015845 | |||||||
chr14:76015963 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.148-6364G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76015963 | |||||||
chr14:76016035 | A | G | 26 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(23): Show |
26 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.148-6292A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016035 | |||||||
chr14:76016102 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.148-6225A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016102 | |||||||
chr14:76016256 | G | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-6071G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016256 | |||||||
chr14:76016269 | G | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0335 |
3 | HG02071.hp1 NA18940.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.148-6058G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016269 | |||||||
chr14:76016273 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.148-6054A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016273 | |||||||
chr14:76016277 | A | G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0245 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-6050A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016277 | |||||||
chr14:76016341 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.148-5986T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016341 | |||||||
chr14:76016347 | C | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.148-5980C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016347 | |||||||
chr14:76016385 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.148-5942T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016385 | |||||||
chr14:76016519 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(5): Show |
9 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-5808A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016519 | |||||||
chr14:76016599 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-5728G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016599 | |||||||
chr14:76016694 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148-5633A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76016694 | |||||||
chr14:76017094 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-5233G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017094 | |||||||
chr14:76017100 | G | C | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-5227G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017100 | |||||||
chr14:76017163 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-5164C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017163 | |||||||
chr14:76017240 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.148-5087T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017240 | |||||||
chr14:76017299 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-5028A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017299 | |||||||
chr14:76017460 | G | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-4867G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017460 | |||||||
chr14:76017693 | G | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-4634G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017693 | |||||||
chr14:76017746 | C | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.148-4581C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017746 | |||||||
chr14:76017756 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.148-4571A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017756 | |||||||
chr14:76017772 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-4555A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017772 | |||||||
chr14:76017837 | T | C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | NA18967.hp2 NA18982.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-4490T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76017837 | |||||||
chr14:76018001 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
7 | HG01175.hp1 HG01928.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-4326C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018001 | |||||||
chr14:76018090 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4237T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018090 | |||||||
chr14:76018161 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4166C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018161 | |||||||
chr14:76018163 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-4164T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018163 | |||||||
chr14:76018242 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-4085T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018242 | |||||||
chr14:76018374 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3953T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018374 | |||||||
chr14:76018378 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3949G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018378 | |||||||
chr14:76018379 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.148-3948A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018379 | |||||||
chr14:76018381 | T | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-3946T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018381 | |||||||
chr14:76018578 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0234 |
3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.148-3749G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018578 | |||||||
chr14:76018849 | C | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.148-3478C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018849 | |||||||
chr14:76018859 | T | G | 1 | a0001c0001t0001g0336 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.148-3468T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018859 | |||||||
chr14:76018952 | C | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-3375C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018952 | |||||||
chr14:76018962 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3365T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018962 | |||||||
chr14:76018968 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0302 a0001c0001t0001g0311 others(3): Show |
7 | HG00673.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3359G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76018968 | |||||||
chr14:76019085 | A | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-3242A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019085 | |||||||
chr14:76019122 | TTTTCTGA others(4): Show |
T | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148-3204_148-3194d others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019122 | |||||||
chr14:76019153 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.148-3174T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019153 | |||||||
chr14:76019191 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-3136A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019191 | |||||||
chr14:76019269 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-3058A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019269 | |||||||
chr14:76019378 | C | CT | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0085 others(10): Show |
15 | HG01106.hp1 HG01433.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.148-2938dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76019378 | ||||||
chr14:76019390 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-2937C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019390 | |||||||
chr14:76019533 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.148-2794T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019533 | |||||||
chr14:76019838 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0060 others(7): Show |
13 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-2489T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019838 | |||||||
chr14:76019887 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148-2440T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019887 | |||||||
chr14:76019944 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.148-2383A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76019944 | |||||||
chr14:76020002 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.148-2325A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020002 | |||||||
chr14:76020132 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.148-2195G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020132 | |||||||
chr14:76020155 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.148-2172A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020155 | |||||||
chr14:76020200 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148-2127C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020200 | |||||||
chr14:76020364 | G | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1963G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020364 | |||||||
chr14:76020386 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.148-1941C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020386 | |||||||
chr14:76020397 | T | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(5): Show |
8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-1930T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020397 | |||||||
chr14:76020455 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-1872A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020455 | |||||||
chr14:76020514 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148-1813A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020514 | |||||||
chr14:76020543 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.148-1784T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020543 | |||||||
chr14:76020683 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148-1644G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020683 | |||||||
chr14:76020687 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-1640G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020687 | |||||||
chr14:76020863 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1464C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020863 | |||||||
chr14:76020864 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.148-1463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76020864 | |||||||
chr14:76021011 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-1316C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021011 | |||||||
chr14:76021141 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.148-1186G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021141 | |||||||
chr14:76021203 | G | C | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148-1124G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021203 | |||||||
chr14:76021309 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-1018A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021309 | |||||||
chr14:76021348 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.148-979A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021348 | |||||||
chr14:76021442 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.148-885A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021442 | |||||||
chr14:76021451 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-876A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021451 | |||||||
chr14:76021478 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(5): Show |
8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-849A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021478 | |||||||
chr14:76021571 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148-756T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021571 | |||||||
chr14:76021923 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-404T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76021923 | |||||||
chr14:76022207 | C | T | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.148-120C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76022207 | |||||||
chr14:76022250 | C | CA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-71dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 76022250 | ||||||
chr14:76022262 | A | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-65A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 2/8 | chr14 | 76022262 | |||||||
chr14:76022507 | C | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+113C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022507 | |||||||
chr14:76022528 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+134A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022528 | |||||||
chr14:76022609 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
40 | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.215+215C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022609 | |||||||
chr14:76022732 | A | G | 5 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0326 others(2): Show |
5 | NA18940.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+338A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022732 | |||||||
chr14:76022741 | C | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.215+347C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022741 | |||||||
chr14:76022790 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.215+396A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022790 | |||||||
chr14:76022929 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.215+535G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76022929 | |||||||
chr14:76023006 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0259 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.215+612C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023006 | |||||||
chr14:76023108 | T | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.215+714T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023108 | |||||||
chr14:76023144 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+750T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023144 | |||||||
chr14:76023171 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+777A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023171 | |||||||
chr14:76023254 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+860A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023254 | |||||||
chr14:76023534 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+1140G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023534 | |||||||
chr14:76023557 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+1163T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023557 | |||||||
chr14:76023735 | A | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0001g0281 others(1): Show |
5 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+1341A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023735 | |||||||
chr14:76023735 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.215+1341A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023735 | |||||||
chr14:76023875 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+1481G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76023875 | |||||||
chr14:76024034 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+1640C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024034 | |||||||
chr14:76024192 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.215+1798T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024192 | |||||||
chr14:76024393 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+1999A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024393 | |||||||
chr14:76024395 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.215+2001C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024395 | |||||||
chr14:76024432 | A | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(48): Show |
60 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.215+2038A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024432 | |||||||
chr14:76024469 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.215+2075G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024469 | |||||||
chr14:76024696 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG00280.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.215+2302G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024696 | |||||||
chr14:76024869 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.215+2475A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024869 | |||||||
chr14:76024885 | T | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+2491T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76024885 | |||||||
chr14:76025084 | TA | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+2698delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76025084 | ||||||
chr14:76025091 | A | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0182 a0001c0001t0001g0339 |
3 | HG00642.hp1 HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.215+2697A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025091 | |||||||
chr14:76025108 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0069 |
3 | HG01074.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.215+2714G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025108 | |||||||
chr14:76025224 | T | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+2830T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025224 | |||||||
chr14:76025256 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.215+2862A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025256 | |||||||
chr14:76025458 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(29): Show |
43 | HG01243.hp1 HG01256.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.215+3064T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025458 | |||||||
chr14:76025582 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.215+3188C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025582 | |||||||
chr14:76025611 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.215+3217A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025611 | |||||||
chr14:76025849 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.215+3455G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025849 | |||||||
chr14:76025890 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.215+3496C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025890 | |||||||
chr14:76025908 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
169 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.215+3514G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025908 | |||||||
chr14:76025924 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+3530G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025924 | |||||||
chr14:76025977 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0255 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.215+3583C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76025977 | |||||||
chr14:76026083 | G | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+3689G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026083 | |||||||
chr14:76026123 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.215+3729G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026123 | |||||||
chr14:76026164 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+3770A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026164 | |||||||
chr14:76026221 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215+3827A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026221 | |||||||
chr14:76026276 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+3882C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026276 | |||||||
chr14:76026349 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215+3955G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026349 | |||||||
chr14:76026372 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+3978G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026372 | |||||||
chr14:76026552 | C | CA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
125 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.215+4177dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026552 | ||||||
chr14:76026552 | CA | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.215+4177delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026552 | ||||||
chr14:76026685 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+4291A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026685 | |||||||
chr14:76026876 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+4482A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76026876 | |||||||
chr14:76026900 | C | CA | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+4514dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76026900 | ||||||
chr14:76027142 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0122 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.215+4748A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027142 | |||||||
chr14:76027252 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+4858A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027252 | |||||||
chr14:76027336 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+4942C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027336 | |||||||
chr14:76027340 | A | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0016 others(118): Show |
130 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.215+4946A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027340 | |||||||
chr14:76027348 | A | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0255 |
2 | HG01069.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+4954A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027348 | |||||||
chr14:76027349 | C | CACTT | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.215+4955_215+4956i others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027349 | |||||||
chr14:76027349 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0255 |
2 | HG01069.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+4955C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027349 | |||||||
chr14:76027365 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
121 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.215+4971A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027365 | |||||||
chr14:76027378 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+4984G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027378 | |||||||
chr14:76027408 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215+5014T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027408 | |||||||
chr14:76027706 | C | CA | 22 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0084 others(19): Show |
23 | HG01167.hp1 HG02027.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.215+5330dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76027706 | ||||||
chr14:76027706 | CA | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(110): Show |
128 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.215+5330delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76027706 | ||||||
chr14:76027720 | A | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+5326A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027720 | |||||||
chr14:76027891 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215+5497G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027891 | |||||||
chr14:76027907 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0072 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+5513T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027907 | |||||||
chr14:76027960 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+5566A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76027960 | |||||||
chr14:76028012 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215+5618C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028012 | |||||||
chr14:76028233 | T | TG | 6 | a0001c0001t0001g0130 a0001c0001t0001g0181 a0001c0001t0001g0189 others(3): Show |
6 | HG01255.hp2 HG01934.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+5843dupG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76028233 | ||||||
chr14:76028241 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+5847C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028241 | |||||||
chr14:76028285 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+5891G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028285 | |||||||
chr14:76028403 | T | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+6009T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028403 | |||||||
chr14:76028748 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.215+6354T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028748 | |||||||
chr14:76028779 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+6385G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028779 | |||||||
chr14:76028894 | C | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+6500C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028894 | |||||||
chr14:76028923 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+6529C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028923 | |||||||
chr14:76028972 | T | C | 1 | a0001c0001t0001g0024 | 2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.215+6578T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028972 | |||||||
chr14:76028978 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+6584C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028978 | |||||||
chr14:76028999 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.215+6605G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76028999 | |||||||
chr14:76029055 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+6661C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029055 | |||||||
chr14:76029153 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+6759T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029153 | |||||||
chr14:76029203 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+6809A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029203 | |||||||
chr14:76029218 | A | G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0245 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+6824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029218 | |||||||
chr14:76029449 | A | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(86): Show |
96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.215+7055A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029449 | |||||||
chr14:76029562 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.215+7168T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029562 | |||||||
chr14:76029579 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+7185T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029579 | |||||||
chr14:76029611 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.215+7217T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029611 | |||||||
chr14:76029851 | T | TTTTATTT others(7): Show |
1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.215+7460_215+7461i others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | T | TTTTTA | 8 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0090 others(5): Show |
8 | HG00597.hp1 HG01168.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+7501_215+7505d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | T | TTTTTATT others(3): Show |
68 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0023 others(65): Show |
72 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.215+7496_215+7505d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | T | TTTTTATT others(8): Show |
75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(72): Show |
88 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.215+7491_215+7505d others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | T | TTTTTATT others(13): Show |
57 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
62 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+7486_215+7505d others(22): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | T | TTTTTATT others(18): Show |
6 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0001t0001g0160 others(3): Show |
6 | HG02683.hp2 HG03704.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+7481_215+7505d others(27): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | TTTTTA | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0289 others(2): Show |
5 | HG02055.hp1 HG02602.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+7501_215+7505d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029851 | TTTTTATT others(3): Show |
T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0342 others(2): Show |
6 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+7496_215+7505d others(12): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029851 | ||||||
chr14:76029868 | T | TTTATTTT others(79): Show |
4 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG02922.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+7505_215+7506i others(88): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | ||||||
chr14:76029868 | T | TTTATTTT others(79): Show |
1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.215+7505_215+7506i others(88): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | ||||||
chr14:76029868 | T | TTTATTTT others(84): Show |
4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0105 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+7505_215+7506i others(93): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029868 | ||||||
chr14:76029871 | A | ATTTTATT others(14): Show |
1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.215+7490_215+7491i others(23): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | ||||||
chr14:76029871 | A | ATTTTATT others(24): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0072 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+7500_215+7501i others(33): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | ||||||
chr14:76029871 | A | ATTTTATT others(39): Show |
1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+7505_215+7506i others(48): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029871 | ||||||
chr14:76029904 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.215+7510C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029904 | |||||||
chr14:76029942 | T | TG | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
118 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.215+7549dupG | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76029942 | ||||||
chr14:76029978 | T | C | 1 | a0001c0001t0001g0341 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.215+7584T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76029978 | |||||||
chr14:76030029 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+7635C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030029 | |||||||
chr14:76030107 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.215+7713C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030107 | |||||||
chr14:76030134 | G | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0279 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.215+7740G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030134 | |||||||
chr14:76030229 | TCA | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(37): Show |
45 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.215+7838_215+7839d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76030229 | ||||||
chr14:76030234 | G | GT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+7849dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76030234 | ||||||
chr14:76030361 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0130 |
2 | NA18967.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.215+7967C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030361 | |||||||
chr14:76030377 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0234 |
3 | HG01358.hp2 HG01516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.215+7983A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030377 | |||||||
chr14:76030397 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.215+8003A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030397 | |||||||
chr14:76030419 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8025A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030419 | |||||||
chr14:76030446 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.215+8052T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030446 | |||||||
chr14:76030472 | G | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+8078G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030472 | |||||||
chr14:76030477 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.215+8083A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030477 | |||||||
chr14:76030528 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8134G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030528 | |||||||
chr14:76030888 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.215+8494G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030888 | |||||||
chr14:76030892 | T | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.215+8498T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030892 | |||||||
chr14:76030979 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215+8585T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030979 | |||||||
chr14:76030980 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.215+8586T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030980 | |||||||
chr14:76030990 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+8596A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76030990 | |||||||
chr14:76031020 | G | GTA | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+8637_215+8638d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76031020 | ||||||
chr14:76031030 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+8636A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031030 | |||||||
chr14:76031058 | T | C | 2 | a0002c0002t0001g0033 a0002c0002t0001g0337 |
3 | HG02056.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.215+8664T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031058 | |||||||
chr14:76031118 | C | T | 8 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(5): Show |
8 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+8724C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031118 | |||||||
chr14:76031378 | C | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+8984C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031378 | |||||||
chr14:76031443 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9049A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031443 | |||||||
chr14:76031500 | G | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+9106G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031500 | |||||||
chr14:76031609 | GAAATAAG others(1): Show |
G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9224_215+9231d others(10): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76031609 | ||||||
chr14:76031679 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+9285C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031679 | |||||||
chr14:76031906 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+9512A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031906 | |||||||
chr14:76031917 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+9523C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76031917 | |||||||
chr14:76032101 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+9707C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032101 | |||||||
chr14:76032200 | C | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+9806C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032200 | |||||||
chr14:76032217 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+9823A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032217 | |||||||
chr14:76032271 | C | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0291 |
2 | NA18987.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.215+9877C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032271 | |||||||
chr14:76032428 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+10034A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032428 | |||||||
chr14:76032492 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.215+10098C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032492 | |||||||
chr14:76032555 | C | G | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG01168.hp1 HG01358.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+10161C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032555 | |||||||
chr14:76032664 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.215+10270C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032664 | |||||||
chr14:76032727 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0152 others(4): Show |
7 | HG01167.hp1 HG02258.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+10333C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032727 | |||||||
chr14:76032757 | G | GA | 3 | a0001c0001t0001g0036 a0001c0001t0001g0290 a0001c0001t0001g0349 |
4 | NA18950.hp1 NA18961.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+10365dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76032757 | ||||||
chr14:76032793 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+10399T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032793 | |||||||
chr14:76032937 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+10543G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76032937 | |||||||
chr14:76033032 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0339 |
2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.215+10638A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033032 | |||||||
chr14:76033109 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.215+10715G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033109 | |||||||
chr14:76033117 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.215+10723G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033117 | |||||||
chr14:76033159 | C | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(129): Show |
142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.215+10765C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033159 | |||||||
chr14:76033348 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.215+10954C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033348 | |||||||
chr14:76033411 | C | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(78): Show |
87 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.215+11017C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033411 | |||||||
chr14:76033836 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.215+11442G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033836 | |||||||
chr14:76033930 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+11536A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033930 | |||||||
chr14:76033960 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.215+11566T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033960 | |||||||
chr14:76033978 | T | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0058 others(9): Show |
14 | HG01070.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.215+11584T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76033978 | |||||||
chr14:76034145 | G | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+11751G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034145 | |||||||
chr14:76034306 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG00423.hp2 HG02129.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.215+11912G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034306 | |||||||
chr14:76034359 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.215+11965T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034359 | |||||||
chr14:76034461 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215+12067A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034461 | |||||||
chr14:76034478 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+12084G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034478 | |||||||
chr14:76034612 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.215+12218T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034612 | |||||||
chr14:76034755 | T | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.215+12361T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034755 | |||||||
chr14:76034850 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.215+12456G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034850 | |||||||
chr14:76034957 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.215+12563T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76034957 | |||||||
chr14:76035238 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+12844A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035238 | |||||||
chr14:76035677 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13283G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035677 | |||||||
chr14:76035724 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+13330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035724 | |||||||
chr14:76035813 | A | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+13419A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035813 | |||||||
chr14:76035866 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13472C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035866 | |||||||
chr14:76035962 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.215+13568G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76035962 | |||||||
chr14:76036111 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215+13717G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036111 | |||||||
chr14:76036160 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+13766C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036160 | |||||||
chr14:76036171 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+13777T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036171 | |||||||
chr14:76036312 | T | TTTCC | 6 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0245 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+13938_215+1394 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76036312 | ||||||
chr14:76036364 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.215+13970T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036364 | |||||||
chr14:76036369 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(10): Show |
21 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.215+13975G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036369 | |||||||
chr14:76036408 | C | CT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.215+14031dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76036408 | ||||||
chr14:76036553 | C | T | 42 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(39): Show |
47 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.215+14159C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036553 | |||||||
chr14:76036554 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0075 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.215+14160G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036554 | |||||||
chr14:76036657 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+14263G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036657 | |||||||
chr14:76036780 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.215+14386A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036780 | |||||||
chr14:76036790 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.215+14396C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036790 | |||||||
chr14:76036844 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+14450T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76036844 | |||||||
chr14:76037118 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0231 a0001c0001t0001g0245 others(2): Show |
5 | HG01167.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+14724A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037118 | |||||||
chr14:76037176 | G | GGTGTA | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
109 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.215+14784_215+1478 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037176 | ||||||
chr14:76037198 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.215+14804C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037198 | |||||||
chr14:76037356 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+14962C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037356 | |||||||
chr14:76037539 | A | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(48): Show |
60 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.215+15145A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037539 | |||||||
chr14:76037613 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+15219G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037613 | |||||||
chr14:76037689 | C | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+15295C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037689 | |||||||
chr14:76037691 | G | GT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(45): Show |
62 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+15310dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037691 | ||||||
chr14:76037691 | G | GTT | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.215+15309_215+1531 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76037691 | ||||||
chr14:76037691 | G | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+15297G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037691 | |||||||
chr14:76037693 | T | TG | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+15299_215+1530 others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037693 | |||||||
chr14:76037736 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.215+15342G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037736 | |||||||
chr14:76037739 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.215+15345T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037739 | |||||||
chr14:76037930 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+15536A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037930 | |||||||
chr14:76037988 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.215+15594T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76037988 | |||||||
chr14:76038072 | C | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(53): Show |
66 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.215+15678C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038072 | |||||||
chr14:76038081 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.215+15687G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038081 | |||||||
chr14:76038246 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+15852C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038246 | |||||||
chr14:76038303 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.215+15909T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038303 | |||||||
chr14:76038354 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215+15960G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038354 | |||||||
chr14:76038357 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+15963A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038357 | |||||||
chr14:76038455 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.215+16061T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038455 | |||||||
chr14:76038636 | TA | T | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | NA18953.hp2 NA18969.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+16243delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038636 | |||||||
chr14:76038642 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.215+16248A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038642 | |||||||
chr14:76038783 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.215+16389T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038783 | |||||||
chr14:76038924 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215+16530T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038924 | |||||||
chr14:76038970 | T | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.215+16576T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76038970 | |||||||
chr14:76039015 | AC | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0236 |
3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.215+16622delC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039015 | |||||||
chr14:76039130 | A | AT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0079 others(9): Show |
15 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.215+16749dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76039130 | ||||||
chr14:76039130 | AT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0027 others(30): Show |
43 | HG01256.hp2 HG01433.hp1 HG01496.hp1 others(40): Show |
intron_variant | MODIFIER | c.215+16749delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76039130 | ||||||
chr14:76039191 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.215+16797G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039191 | |||||||
chr14:76039252 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.215+16858C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039252 | |||||||
chr14:76039259 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.215+16865A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039259 | |||||||
chr14:76039268 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01256.hp1 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.215+16874G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039268 | |||||||
chr14:76039315 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.215+16921T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039315 | |||||||
chr14:76039320 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+16926G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039320 | |||||||
chr14:76039327 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.215+16933T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039327 | |||||||
chr14:76039407 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.215+17013C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039407 | |||||||
chr14:76039570 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(12): Show |
16 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.215+17176A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039570 | |||||||
chr14:76039610 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0302 a0001c0001t0001g0311 others(3): Show |
7 | HG00673.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+17216C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76039610 | |||||||
chr14:76040301 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(6): Show |
10 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+17907G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040301 | |||||||
chr14:76040385 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(6): Show |
10 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+17991T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040385 | |||||||
chr14:76040523 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0259 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.216-18119T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040523 | |||||||
chr14:76040709 | C | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG01952.hp2 HG02004.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-17933C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040709 | |||||||
chr14:76040779 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.216-17863G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040779 | |||||||
chr14:76040801 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0290 a0001c0001t0001g0349 |
4 | NA18950.hp1 NA18961.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-17841G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040801 | |||||||
chr14:76040840 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.216-17802C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040840 | |||||||
chr14:76040898 | G | T | 1 | a0001c0001t0001g0036 | 2 | NA18950.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.216-17744G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040898 | |||||||
chr14:76040956 | C | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.216-17686C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76040956 | |||||||
chr14:76041116 | A | G | 39 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(36): Show |
43 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.216-17526A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041116 | |||||||
chr14:76041161 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0001g0273 others(2): Show |
6 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-17481G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041161 | |||||||
chr14:76041391 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0072 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-17251T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041391 | |||||||
chr14:76041491 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.216-17151A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041491 | |||||||
chr14:76041539 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-17103C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041539 | |||||||
chr14:76041576 | T | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-17066T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041576 | |||||||
chr14:76041717 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-16925C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041717 | |||||||
chr14:76041750 | G | T | 1 | a0001c0001t0001g0316 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.216-16892G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041750 | |||||||
chr14:76041750 | GT | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.216-16882delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76041750 | ||||||
chr14:76041752 | T | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(89): Show |
99 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.216-16890T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76041752 | |||||||
chr14:76042073 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-16569G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042073 | |||||||
chr14:76042104 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.216-16538G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042104 | |||||||
chr14:76042107 | G | GAC | 109 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
118 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.216-16516_216-1651 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042107 | ||||||
chr14:76042107 | G | GACAC | 3 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0001t0001g0181 |
3 | HG01081.hp2 HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.216-16518_216-1651 others(8): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042107 | ||||||
chr14:76042127 | C | CAT | 4 | a0001c0001t0001g0141 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01358.hp2 HG01516.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-16515_216-1651 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042127 | |||||||
chr14:76042257 | T | TA | 6 | a0001c0001t0001g0110 a0001c0001t0001g0159 a0001c0001t0001g0166 others(3): Show |
6 | NA18953.hp2 NA18972.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-16369dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76042257 | ||||||
chr14:76042289 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.216-16353C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042289 | |||||||
chr14:76042427 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.216-16215G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042427 | |||||||
chr14:76042436 | C | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-16206C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042436 | |||||||
chr14:76042469 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-16173A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042469 | |||||||
chr14:76042547 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-16095G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042547 | |||||||
chr14:76042629 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0044 others(7): Show |
12 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.216-16013T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042629 | |||||||
chr14:76042702 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0345 |
3 | HG03491.hp2 HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.216-15940C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76042702 | |||||||
chr14:76043023 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.216-15619G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043023 | |||||||
chr14:76043153 | G | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-15489G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043153 | |||||||
chr14:76043227 | T | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-15415T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043227 | |||||||
chr14:76043369 | C | CTCGTG | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.216-15271_216-1526 others(9): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043369 | ||||||
chr14:76043471 | A | AT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
7 | HG01192.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-15158dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043471 | ||||||
chr14:76043471 | A | ATT | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-15159_216-1515 others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76043471 | ||||||
chr14:76043490 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-15152G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043490 | |||||||
chr14:76043490 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216-15152G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043490 | |||||||
chr14:76043525 | G | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(87): Show |
97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.216-15117G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043525 | |||||||
chr14:76043526 | G | A | 5 | a0001c0001t0001g0310 a0001c0001t0001g0321 a0001c0001t0001g0330 others(2): Show |
5 | NA18974.hp2 NA18981.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-15116G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043526 | |||||||
chr14:76043568 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216-15074G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043568 | |||||||
chr14:76043690 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216-14952T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043690 | |||||||
chr14:76043818 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.216-14824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043818 | |||||||
chr14:76043877 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-14765G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043877 | |||||||
chr14:76043898 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.216-14744C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76043898 | |||||||
chr14:76044052 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0231 others(1): Show |
4 | HG01167.hp1 HG02965.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-14590T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044052 | |||||||
chr14:76044143 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0231 others(1): Show |
4 | HG01167.hp1 HG02965.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-14499G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044143 | |||||||
chr14:76044193 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-14449C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044193 | |||||||
chr14:76044198 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.216-14444C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044198 | |||||||
chr14:76044260 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0050 |
2 | NA19070.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.216-14382G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044260 | |||||||
chr14:76044320 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0212 a0001c0001t0001g0243 |
3 | HG01109.hp1 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.216-14322G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044320 | |||||||
chr14:76044347 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.216-14295A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044347 | |||||||
chr14:76044660 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG01070.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.216-13982C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044660 | |||||||
chr14:76044702 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-13940G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044702 | |||||||
chr14:76044712 | A | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0345 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-13930A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044712 | |||||||
chr14:76044777 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-13865G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044777 | |||||||
chr14:76044797 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.216-13845T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044797 | |||||||
chr14:76044963 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.216-13679C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76044963 | |||||||
chr14:76045052 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-13590T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045052 | |||||||
chr14:76045185 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0112 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.216-13457G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045185 | |||||||
chr14:76045191 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-13451A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045191 | |||||||
chr14:76045363 | G | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(47): Show |
59 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.216-13279G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045363 | |||||||
chr14:76045455 | A | G | 24 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(21): Show |
27 | HG00642.hp2 HG01123.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.216-13187A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045455 | |||||||
chr14:76045631 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.216-13011G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045631 | |||||||
chr14:76045654 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-12988C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045654 | |||||||
chr14:76045655 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0231 |
2 | HG01167.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.216-12987G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045655 | |||||||
chr14:76045655 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0243 |
2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.216-12987G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045655 | |||||||
chr14:76045782 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.216-12860G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045782 | |||||||
chr14:76045803 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-12839T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045803 | |||||||
chr14:76045955 | G | A | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.216-12687G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045955 | |||||||
chr14:76045997 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.216-12645T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76045997 | |||||||
chr14:76046271 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0268 a0001c0001t0001g0272 |
4 | NA18943.hp2 NA18955.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-12371C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046271 | |||||||
chr14:76046297 | G | C | 1 | a0001c0001t0001g0311 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.216-12345G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046297 | |||||||
chr14:76046447 | G | T | 1 | a0001c0001t0001g0336 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.216-12195G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046447 | |||||||
chr14:76046537 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.216-12105A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046537 | |||||||
chr14:76046818 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-11824A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046818 | |||||||
chr14:76046904 | A | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-11738A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046904 | |||||||
chr14:76046933 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.216-11709C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046933 | |||||||
chr14:76046982 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.216-11660A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76046982 | |||||||
chr14:76047031 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.216-11611G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047031 | |||||||
chr14:76047249 | G | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | NA18967.hp2 NA18982.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.216-11393G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047249 | |||||||
chr14:76047334 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-11308T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047334 | |||||||
chr14:76047420 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.216-11222G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047420 | |||||||
chr14:76047703 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(5): Show |
9 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-10939G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047703 | |||||||
chr14:76047733 | C | CT | 16 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0063 others(13): Show |
17 | HG00597.hp1 HG01074.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.216-10894dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76047733 | ||||||
chr14:76047970 | C | A | 27 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.216-10672C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047970 | |||||||
chr14:76047979 | G | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-10663G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76047979 | |||||||
chr14:76048125 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
38 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.216-10517G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048125 | |||||||
chr14:76048142 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.216-10500T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048142 | |||||||
chr14:76048147 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0345 |
2 | HG03688.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.216-10495C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048147 | |||||||
chr14:76048242 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
7 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-10400C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048242 | |||||||
chr14:76048681 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.216-9961C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048681 | |||||||
chr14:76048691 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-9951A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048691 | |||||||
chr14:76048830 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.216-9812C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048830 | |||||||
chr14:76048860 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0154 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.216-9782G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048860 | |||||||
chr14:76048870 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216-9772C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048870 | |||||||
chr14:76048881 | T | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.216-9761T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048881 | |||||||
chr14:76048890 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-9752A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048890 | |||||||
chr14:76048970 | A | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(33): Show |
37 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.216-9672A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048970 | |||||||
chr14:76048996 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.216-9646C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76048996 | |||||||
chr14:76049191 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0195 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.216-9451A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049191 | |||||||
chr14:76049216 | C | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0168 |
3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.216-9426C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049216 | |||||||
chr14:76049223 | T | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18747.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.216-9419T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049223 | |||||||
chr14:76049408 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-9234A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049408 | |||||||
chr14:76049457 | GT | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
193 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.216-9171delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049457 | ||||||
chr14:76049457 | GTT | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.216-9172_216-9171d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049457 | ||||||
chr14:76049460 | T | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.216-9182T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049460 | |||||||
chr14:76049461 | T | G | 2 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.216-9181T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049461 | |||||||
chr14:76049486 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(16): Show |
28 | HG01256.hp2 HG01943.hp2 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.216-9156A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049486 | |||||||
chr14:76049517 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-9125G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049517 | |||||||
chr14:76049532 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.216-9110A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76049532 | |||||||
chr14:76049728 | A | ACTT | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.216-8912_216-8910d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049728 | ||||||
chr14:76049866 | G | GC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-8771dupC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76049866 | ||||||
chr14:76050078 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-8564G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050078 | |||||||
chr14:76050199 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0306 a0001c0001t0001g0307 |
4 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-8443C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050199 | |||||||
chr14:76050219 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.216-8423C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050219 | |||||||
chr14:76050403 | G | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.216-8239G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050403 | |||||||
chr14:76050429 | T | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.216-8213T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050429 | |||||||
chr14:76050458 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0150 a0001c0001t0001g0158 others(4): Show |
8 | HG02056.hp1 HG02132.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.216-8184T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050458 | |||||||
chr14:76050519 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.216-8123G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050519 | |||||||
chr14:76050606 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.216-8036A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050606 | |||||||
chr14:76050627 | TGA | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-8011_216-8010d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76050627 | ||||||
chr14:76050633 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.216-8009T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050633 | |||||||
chr14:76050703 | C | T | 18 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0049 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.216-7939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050703 | |||||||
chr14:76050820 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-7822G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050820 | |||||||
chr14:76050821 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-7821G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76050821 | |||||||
chr14:76051009 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.216-7633G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051009 | |||||||
chr14:76051024 | T | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-7618T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051024 | |||||||
chr14:76051104 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-7538G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051104 | |||||||
chr14:76051108 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-7534T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051108 | |||||||
chr14:76051219 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216-7423G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051219 | |||||||
chr14:76051457 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.216-7185G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051457 | |||||||
chr14:76051502 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-7140T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051502 | |||||||
chr14:76051622 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.216-7020C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051622 | |||||||
chr14:76051903 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216-6739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051903 | |||||||
chr14:76051944 | C | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-6698C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051944 | |||||||
chr14:76051996 | C | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-6646C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76051996 | |||||||
chr14:76052047 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0195 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.216-6595C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052047 | |||||||
chr14:76052305 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0186 others(1): Show |
4 | NA18939.hp1 NA18974.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-6337A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052305 | |||||||
chr14:76052317 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-6325G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052317 | |||||||
chr14:76052584 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0236 |
3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.216-6058C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052584 | |||||||
chr14:76052787 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-5855G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052787 | |||||||
chr14:76052790 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(87): Show |
96 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.216-5852G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052790 | |||||||
chr14:76052803 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0087 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.216-5839A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76052803 | |||||||
chr14:76053031 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0065 others(1): Show |
4 | HG01928.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-5611A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053031 | |||||||
chr14:76053076 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0138 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216-5566G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053076 | |||||||
chr14:76053312 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-5330A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053312 | |||||||
chr14:76053385 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.216-5257A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053385 | |||||||
chr14:76053462 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-5180A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053462 | |||||||
chr14:76053499 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-5143C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053499 | |||||||
chr14:76053572 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.216-5070G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053572 | |||||||
chr14:76053633 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.216-5009C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053633 | |||||||
chr14:76053634 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.216-5008G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053634 | |||||||
chr14:76053650 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.216-4992A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053650 | |||||||
chr14:76053733 | A | C | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-4909A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053733 | |||||||
chr14:76053844 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-4798G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76053844 | |||||||
chr14:76054026 | C | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.216-4616C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054026 | |||||||
chr14:76054081 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-4561A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054081 | |||||||
chr14:76054176 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-4466G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054176 | |||||||
chr14:76054256 | G | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-4386G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054256 | |||||||
chr14:76054304 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.216-4338A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054304 | |||||||
chr14:76054416 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.216-4226G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054416 | |||||||
chr14:76054495 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4147T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054495 | |||||||
chr14:76054503 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4139A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054503 | |||||||
chr14:76054536 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0001t0001g0181 |
3 | HG01081.hp2 HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.216-4106G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054536 | |||||||
chr14:76054546 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-4096T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054546 | |||||||
chr14:76054657 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-3985G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054657 | |||||||
chr14:76054667 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.216-3975T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054667 | |||||||
chr14:76054724 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-3918G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76054724 | |||||||
chr14:76055065 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216-3577C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055065 | |||||||
chr14:76055076 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.216-3566G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055076 | |||||||
chr14:76055216 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216-3426C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055216 | |||||||
chr14:76055232 | GCTA | G | 2 | a0002c0002t0001g0033 a0002c0002t0001g0337 |
3 | HG02056.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.216-3407_216-3405d others(5): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76055232 | ||||||
chr14:76055267 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.216-3375A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055267 | |||||||
chr14:76055278 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.216-3364T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055278 | |||||||
chr14:76055310 | C | A | 38 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
42 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.216-3332C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055310 | |||||||
chr14:76055429 | A | G | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.216-3213A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055429 | |||||||
chr14:76055467 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216-3175G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055467 | |||||||
chr14:76055470 | T | C | 2 | a0001c0001t0001g0315 a0001c0001t0001g0325 |
2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.216-3172T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055470 | |||||||
chr14:76055487 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0072 |
3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.216-3155A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055487 | |||||||
chr14:76055511 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-3131A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055511 | |||||||
chr14:76055535 | C | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.216-3107C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055535 | |||||||
chr14:76055684 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00609.hp2 NA18964.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-2958A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055684 | |||||||
chr14:76055737 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.216-2905C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055737 | |||||||
chr14:76055856 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.216-2786G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055856 | |||||||
chr14:76055951 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0174 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.216-2691G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055951 | |||||||
chr14:76055961 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.216-2681A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76055961 | |||||||
chr14:76056020 | A | C | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216-2622A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056020 | |||||||
chr14:76056036 | T | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG01123.hp2 HG01361.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.216-2606T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056036 | |||||||
chr14:76056269 | C | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-2373C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056269 | |||||||
chr14:76056289 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.216-2353C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056289 | |||||||
chr14:76056290 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216-2352G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056290 | |||||||
chr14:76056309 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2333G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056309 | |||||||
chr14:76056415 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0168 |
3 | NA18946.hp2 NA18964.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.216-2227A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056415 | |||||||
chr14:76056535 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.216-2107G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056535 | |||||||
chr14:76056543 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.216-2099T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056543 | |||||||
chr14:76056848 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.216-1794G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056848 | |||||||
chr14:76056851 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0111 |
2 | HG02602.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.216-1791C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056851 | |||||||
chr14:76056984 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.216-1658T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76056984 | |||||||
chr14:76057010 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216-1632A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057010 | |||||||
chr14:76057242 | A | AT | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-1392dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057242 | ||||||
chr14:76057274 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.216-1368T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057274 | |||||||
chr14:76057287 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.216-1355A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057287 | |||||||
chr14:76057293 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-1349G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057293 | |||||||
chr14:76057438 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.216-1204A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057438 | |||||||
chr14:76057553 | CA | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.216-1075delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057553 | ||||||
chr14:76057680 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.216-962G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057680 | |||||||
chr14:76057901 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.216-741A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057901 | |||||||
chr14:76057960 | T | TA | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-677dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76057960 | ||||||
chr14:76057966 | T | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-676T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76057966 | |||||||
chr14:76058081 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.216-561C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058081 | |||||||
chr14:76058106 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.216-536C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058106 | |||||||
chr14:76058332 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.216-310A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058332 | |||||||
chr14:76058450 | G | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0087 others(8): Show |
12 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.216-192G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058450 | |||||||
chr14:76058625 | T | G | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-17T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | chr14 | 76058625 | |||||||
chr14:76058627 | CT | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
132 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(129): Show |
splice_region_variant&intron_variant | LOW | c.216-4delT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 76058627 | ||||||
chr14:76059033 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.249-294T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059033 | |||||||
chr14:76059055 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.249-272A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059055 | |||||||
chr14:76059163 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0128 a0001c0001t0001g0139 others(1): Show |
4 | HG02040.hp1 HG02683.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-164G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059163 | |||||||
chr14:76059172 | A | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.249-155A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059172 | |||||||
chr14:76059210 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.249-117A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059210 | |||||||
chr14:76059277 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.249-50C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059277 | |||||||
chr14:76059278 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.249-49G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 4/8 | chr14 | 76059278 | |||||||
chr14:76059719 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.295+346A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059719 | |||||||
chr14:76059765 | T | A | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+392T>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059765 | |||||||
chr14:76059770 | A | G | 66 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(63): Show |
71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.295+397A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76059770 | |||||||
chr14:76060030 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+657C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060030 | |||||||
chr14:76060033 | A | G | 1 | a0001c0001t0001g0336 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.295+660A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060033 | |||||||
chr14:76060042 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0079 others(6): Show |
12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+669A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060042 | |||||||
chr14:76060046 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.295+673A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060046 | |||||||
chr14:76060179 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.295+806A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060179 | |||||||
chr14:76060313 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+940G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060313 | |||||||
chr14:76060428 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
147 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.295+1055A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060428 | |||||||
chr14:76060534 | C | CT | 92 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(89): Show |
98 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.295+1171dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060534 | ||||||
chr14:76060825 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+1452C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060825 | |||||||
chr14:76060825 | CCTTT | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+1456_295+1459d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060825 | ||||||
chr14:76060828 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.295+1455T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060828 | |||||||
chr14:76060829 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.295+1456T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060829 | |||||||
chr14:76060829 | T | TCTTC | 22 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0108 others(19): Show |
23 | HG00408.hp1 HG00673.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+1485_295+1488d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060829 | ||||||
chr14:76060829 | TCTTC | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.295+1485_295+1488d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060829 | ||||||
chr14:76060832 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1459T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060832 | |||||||
chr14:76060837 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
113 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.295+1464C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060837 | |||||||
chr14:76060857 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.295+1484C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060857 | |||||||
chr14:76060864 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+1491T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76060864 | |||||||
chr14:76060881 | T | TCTCCC | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1517_295+1521d others(7): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76060881 | ||||||
chr14:76061019 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+1646A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061019 | |||||||
chr14:76061063 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1690G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061063 | |||||||
chr14:76061072 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+1699G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061072 | |||||||
chr14:76061105 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+1732T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061105 | |||||||
chr14:76061148 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.295+1775C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061148 | |||||||
chr14:76061271 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.295+1898C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061271 | |||||||
chr14:76061306 | C | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+1933C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061306 | |||||||
chr14:76061313 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0079 others(6): Show |
12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+1940G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061313 | |||||||
chr14:76061459 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+2086A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061459 | |||||||
chr14:76061517 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295+2144A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061517 | |||||||
chr14:76061641 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.295+2268T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061641 | |||||||
chr14:76061943 | T | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2570T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76061943 | |||||||
chr14:76062008 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.295+2635T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062008 | |||||||
chr14:76062021 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+2648A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062021 | |||||||
chr14:76062089 | T | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.295+2716T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062089 | |||||||
chr14:76062216 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2843G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062216 | |||||||
chr14:76062227 | C | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.295+2854C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062227 | |||||||
chr14:76062237 | A | AT | 5 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0001g0273 others(2): Show |
6 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+2870dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062237 | ||||||
chr14:76062312 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.295+2939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062312 | |||||||
chr14:76062333 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0148 others(7): Show |
11 | HG01106.hp2 HG01175.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+2960G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062333 | |||||||
chr14:76062365 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.295+2992C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062365 | |||||||
chr14:76062371 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.295+2998G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062371 | |||||||
chr14:76062489 | A | G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0245 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+3116A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062489 | |||||||
chr14:76062590 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0118 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+3217G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062590 | |||||||
chr14:76062611 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+3238A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062611 | |||||||
chr14:76062637 | TCAGGCGC others(10551): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.295+3269_296-9096d others(2): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062637 | ||||||
chr14:76062642 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+3269C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062642 | |||||||
chr14:76062710 | A | AG | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.295+3337_295+3338i others(3): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062710 | |||||||
chr14:76062743 | G | A | 1 | a0001c0004t0001g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.295+3370G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062743 | |||||||
chr14:76062747 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.295+3374C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062747 | |||||||
chr14:76062809 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.295+3436C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062809 | |||||||
chr14:76062917 | C | CA | 18 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0032 others(15): Show |
20 | HG00408.hp1 HG00673.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.295+3568dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0087 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.295+3555_295+3568d others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0049 a0001c0001t0001g0231 |
2 | HG01167.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.295+3554_295+3568d others(17): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG02258.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.295+3553_295+3568d others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.295+3551_295+3568d others(20): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295+3547_295+3568d others(24): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | CA | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0042 others(14): Show |
17 | HG00597.hp1 HG00642.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+3568delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | CAA | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(78): Show |
85 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.295+3567_295+3568d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | CAAAA | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(42): Show |
53 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.295+3565_295+3568d others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062917 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.295+3557_295+3568d others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062917 | ||||||
chr14:76062936 | A | AAAAG | 7 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(4): Show |
8 | HG01891.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+3566_295+3567i others(6): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062936 | ||||||
chr14:76062938 | A | AAAAAAAG others(7): Show |
13 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0041 others(10): Show |
13 | HG00642.hp2 HG01192.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(16): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | ||||||
chr14:76062938 | A | AAAAAAGA others(6): Show |
88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(85): Show |
96 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(15): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | ||||||
chr14:76062938 | A | AAAAAGAA others(5): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0122 others(5): Show |
9 | HG01167.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+3568_295+3569i others(14): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76062938 | ||||||
chr14:76062947 | T | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG01952.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.295+3574T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062947 | |||||||
chr14:76062948 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.295+3575A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062948 | |||||||
chr14:76062954 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+3581A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062954 | |||||||
chr14:76062991 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295+3618T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76062991 | |||||||
chr14:76063093 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+3720T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063093 | |||||||
chr14:76063110 | A | G | 1 | a0001c0001t0001g0322 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.295+3737A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063110 | |||||||
chr14:76063234 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+3861C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063234 | |||||||
chr14:76063340 | G | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18747.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.295+3967G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063340 | |||||||
chr14:76063597 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.295+4224A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063597 | |||||||
chr14:76063602 | C | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
27 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.295+4229C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063602 | |||||||
chr14:76063953 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.295+4580G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76063953 | |||||||
chr14:76064079 | C | CT | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+4707dupT | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76064079 | ||||||
chr14:76064295 | A | T | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.295+4922A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064295 | |||||||
chr14:76064332 | C | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+4959C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064332 | |||||||
chr14:76064360 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+4987C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064360 | |||||||
chr14:76064476 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0231 |
2 | HG01167.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.295+5103C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064476 | |||||||
chr14:76064567 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+5194G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064567 | |||||||
chr14:76064569 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0279 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.295+5196G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064569 | |||||||
chr14:76064578 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+5205G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064578 | |||||||
chr14:76064583 | A | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
33 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+5210A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064583 | |||||||
chr14:76064651 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+5278C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064651 | |||||||
chr14:76064797 | C | T | 28 | a0001c0001t0001g0046 a0001c0001t0001g0130 a0001c0001t0001g0201 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.295+5424C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064797 | |||||||
chr14:76064859 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.295+5486C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064859 | |||||||
chr14:76064920 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
83 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.295+5547T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76064920 | |||||||
chr14:76065090 | C | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+5717C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065090 | |||||||
chr14:76065106 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+5733C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065106 | |||||||
chr14:76065122 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0255 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.295+5749T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065122 | |||||||
chr14:76065130 | T | C | 27 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.295+5757T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065130 | |||||||
chr14:76065166 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+5793A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065166 | |||||||
chr14:76065378 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+6005G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065378 | |||||||
chr14:76065479 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.295+6106G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065479 | |||||||
chr14:76065568 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0237 |
2 | HG00099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.295+6195C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065568 | |||||||
chr14:76065570 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(56): Show |
69 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.295+6197A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065570 | |||||||
chr14:76065715 | G | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+6342G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065715 | |||||||
chr14:76065872 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295+6499G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065872 | |||||||
chr14:76065880 | G | T | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295+6507G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065880 | |||||||
chr14:76065998 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295+6625C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76065998 | |||||||
chr14:76066045 | C | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+6672C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066045 | |||||||
chr14:76066084 | C | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
81 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.295+6711C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066084 | |||||||
chr14:76066350 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.295+6977G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066350 | |||||||
chr14:76066536 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
57 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.295+7163C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066536 | |||||||
chr14:76066608 | C | T | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
152 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.295+7235C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066608 | |||||||
chr14:76066697 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.295+7324T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066697 | |||||||
chr14:76066702 | A | G | 3 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0236 |
3 | HG02165.hp1 NA18978.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.295+7329A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066702 | |||||||
chr14:76066768 | A | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+7395A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066768 | |||||||
chr14:76066785 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.295+7412G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76066785 | |||||||
chr14:76067112 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(30): Show |
39 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.295+7739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067112 | |||||||
chr14:76067288 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.295+7915G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067288 | |||||||
chr14:76067419 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+8046A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067419 | |||||||
chr14:76067427 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.295+8054G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067427 | |||||||
chr14:76067527 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0075 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.295+8154A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067527 | |||||||
chr14:76067568 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.295+8195T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067568 | |||||||
chr14:76067579 | C | CA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(37): Show |
45 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.295+8219dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | ||||||
chr14:76067579 | C | CAA | 24 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0205 others(21): Show |
24 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.295+8218_295+8219d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | ||||||
chr14:76067579 | CA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0046 others(3): Show |
6 | HG01070.hp1 HG02451.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+8219delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76067579 | ||||||
chr14:76067603 | G | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+8230G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067603 | |||||||
chr14:76067622 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.295+8249T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067622 | |||||||
chr14:76067765 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+8392C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067765 | |||||||
chr14:76067773 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(13): Show |
17 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.295+8400C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067773 | |||||||
chr14:76067810 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.295+8437T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76067810 | |||||||
chr14:76068225 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+8852A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068225 | |||||||
chr14:76068252 | A | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+8879A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068252 | |||||||
chr14:76068344 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.295+8971C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068344 | |||||||
chr14:76068634 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+9261T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068634 | |||||||
chr14:76068804 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
82 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.295+9431G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068804 | |||||||
chr14:76068852 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.295+9479A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068852 | |||||||
chr14:76068893 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
2 | NA18992.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.295+9520A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068893 | |||||||
chr14:76068896 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+9523G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068896 | |||||||
chr14:76068989 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+9616A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76068989 | |||||||
chr14:76069125 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.295+9752A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069125 | |||||||
chr14:76069307 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.295+9934G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069307 | |||||||
chr14:76069318 | C | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0158 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.295+9945C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069318 | |||||||
chr14:76069464 | A | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0330 |
2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.295+10091A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069464 | |||||||
chr14:76069513 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+10140A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069513 | |||||||
chr14:76069742 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.295+10369G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069742 | |||||||
chr14:76069826 | C | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0330 |
2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.295+10453C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069826 | |||||||
chr14:76069899 | C | T | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+10526C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76069899 | |||||||
chr14:76070502 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(12): Show |
16 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.295+11129G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070502 | |||||||
chr14:76070874 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.296-11421C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070874 | |||||||
chr14:76070918 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-11377T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070918 | |||||||
chr14:76070950 | T | G | 1 | a0001c0001t0001g0334 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.296-11345T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76070950 | |||||||
chr14:76071043 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.296-11252G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071043 | |||||||
chr14:76071282 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0166 |
2 | NA18939.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.296-11013G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071282 | |||||||
chr14:76071478 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-10817G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071478 | |||||||
chr14:76071534 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.296-10761A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071534 | |||||||
chr14:76071591 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.296-10704G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071591 | |||||||
chr14:76071841 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.296-10454G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071841 | |||||||
chr14:76071891 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-10404C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071891 | |||||||
chr14:76071969 | C | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-10326C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76071969 | |||||||
chr14:76072439 | A | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-9856A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072439 | |||||||
chr14:76072700 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-9595T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072700 | |||||||
chr14:76072739 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0309 |
3 | HG03491.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.296-9556A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072739 | |||||||
chr14:76072832 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(11): Show |
15 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-9463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072832 | |||||||
chr14:76072923 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01928.hp1 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.296-9372A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072923 | |||||||
chr14:76072978 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0148 others(7): Show |
11 | HG01106.hp2 HG01175.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.296-9317G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072978 | |||||||
chr14:76072992 | C | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-9303C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76072992 | |||||||
chr14:76073222 | A | G | 27 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-9073A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073222 | |||||||
chr14:76073251 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0138 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.296-9044G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073251 | |||||||
chr14:76073266 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.296-9029G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073266 | |||||||
chr14:76073490 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-8805C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073490 | |||||||
chr14:76073577 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0001g0294 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.296-8707_296-8680d others(30): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76073577 | ||||||
chr14:76073607 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.296-8688G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073607 | |||||||
chr14:76073814 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-8481C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073814 | |||||||
chr14:76073834 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.296-8461T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073834 | |||||||
chr14:76073866 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-8429C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073866 | |||||||
chr14:76073930 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.296-8365C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073930 | |||||||
chr14:76073937 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.296-8358G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76073937 | |||||||
chr14:76074021 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-8274G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074021 | |||||||
chr14:76074246 | T | C | 27 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(24): Show |
27 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-8049T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074246 | |||||||
chr14:76074255 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-8040T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074255 | |||||||
chr14:76074267 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-8028G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074267 | |||||||
chr14:76074339 | T | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-7956T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074339 | |||||||
chr14:76074405 | G | GA | 12 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.296-7889dupA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76074405 | ||||||
chr14:76074576 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-7719G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074576 | |||||||
chr14:76074578 | T | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-7717T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074578 | |||||||
chr14:76074618 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-7677T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074618 | |||||||
chr14:76074808 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-7487C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074808 | |||||||
chr14:76074809 | C | T | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | HG02040.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.296-7486C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074809 | |||||||
chr14:76074823 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.296-7472C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074823 | |||||||
chr14:76074839 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.296-7456C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76074839 | |||||||
chr14:76075012 | G | C | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-7283G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075012 | |||||||
chr14:76075030 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.296-7265G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075030 | |||||||
chr14:76075329 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6966T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075329 | |||||||
chr14:76075378 | CA | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-6916delA | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075378 | |||||||
chr14:76075384 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-6911A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075384 | |||||||
chr14:76075572 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.296-6723G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075572 | |||||||
chr14:76075606 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6689T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075606 | |||||||
chr14:76075675 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.296-6620A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075675 | |||||||
chr14:76075680 | A | G | 3 | a0001c0001t0001g0303 a0001c0001t0001g0314 a0001c0001t0001g0317 |
3 | NA18984.hp2 NA18986.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.296-6615A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075680 | |||||||
chr14:76075695 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0060 others(4): Show |
10 | HG01081.hp1 HG01243.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.296-6600C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075695 | |||||||
chr14:76075754 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-6541G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075754 | |||||||
chr14:76075941 | G | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6354G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075941 | |||||||
chr14:76075962 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-6333C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76075962 | |||||||
chr14:76076014 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0194 others(1): Show |
4 | HG00438.hp1 NA18991.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-6281G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076014 | |||||||
chr14:76076039 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-6256C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076039 | |||||||
chr14:76076071 | T | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-6224T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076071 | |||||||
chr14:76076149 | G | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-6146G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076149 | |||||||
chr14:76076159 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.296-6136G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076159 | |||||||
chr14:76076262 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-6033G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076262 | |||||||
chr14:76076507 | AGATTTAT others(9): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-5785_296-5770d others(18): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76076507 | ||||||
chr14:76076513 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
109 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.296-5782A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076513 | |||||||
chr14:76076661 | G | A | 66 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(63): Show |
71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.296-5634G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076661 | |||||||
chr14:76076908 | AC | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0096 others(1): Show |
4 | HG02922.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-5384delC | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76076908 | ||||||
chr14:76076932 | C | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-5363C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76076932 | |||||||
chr14:76077013 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
118 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.296-5282A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077013 | |||||||
chr14:76077030 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
172 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.296-5265A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077030 | |||||||
chr14:76077165 | T | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0081 others(3): Show |
8 | HG00099.hp1 HG00733.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-5130T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077165 | |||||||
chr14:76077215 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(6): Show |
10 | HG01884.hp1 HG01891.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.296-5080C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077215 | |||||||
chr14:76077219 | G | GCT | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.296-5072_296-5071d others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76077219 | ||||||
chr14:76077317 | T | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.296-4978T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077317 | |||||||
chr14:76077358 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-4937C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077358 | |||||||
chr14:76077425 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-4870C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077425 | |||||||
chr14:76077556 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-4739G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077556 | |||||||
chr14:76077578 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0342 a0001c0001t0001g0343 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-4717C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077578 | |||||||
chr14:76077894 | A | G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0250 others(7): Show |
11 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-4401A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76077894 | |||||||
chr14:76078119 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.296-4176C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078119 | |||||||
chr14:76078159 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-4136G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078159 | |||||||
chr14:76078194 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-4101G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078194 | |||||||
chr14:76078656 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.296-3639T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078656 | |||||||
chr14:76078732 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.296-3563C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078732 | |||||||
chr14:76078736 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
55 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.296-3559G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078736 | |||||||
chr14:76078743 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-3552G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078743 | |||||||
chr14:76078820 | T | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-3475T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078820 | |||||||
chr14:76078912 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.296-3383C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078912 | |||||||
chr14:76078917 | T | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(36): Show |
44 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.296-3378T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76078917 | |||||||
chr14:76078983 | TTAGCATA others(4): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.296-3308_296-3298d others(13): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr14 | 76078983 | ||||||
chr14:76079001 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.296-3294T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079001 | |||||||
chr14:76079080 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.296-3215C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079080 | |||||||
chr14:76079149 | A | G | 13 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.296-3146A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079149 | |||||||
chr14:76079410 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | NA18960.hp1 NA18963.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-2885T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079410 | |||||||
chr14:76079520 | T | G | 1 | a0001c0001t0001g0300 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-2775T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079520 | |||||||
chr14:76079703 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.296-2592G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079703 | |||||||
chr14:76079816 | G | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
171 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.296-2479G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079816 | |||||||
chr14:76079832 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.296-2463G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079832 | |||||||
chr14:76079863 | T | G | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-2432T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079863 | |||||||
chr14:76079947 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.296-2348G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76079947 | |||||||
chr14:76080072 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.296-2223G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080072 | |||||||
chr14:76080127 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-2168C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080127 | |||||||
chr14:76080208 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.296-2087C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080208 | |||||||
chr14:76080282 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.296-2013G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080282 | |||||||
chr14:76080423 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.296-1872C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080423 | |||||||
chr14:76080472 | C | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1823C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080472 | |||||||
chr14:76080593 | C | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1702C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080593 | |||||||
chr14:76080667 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.296-1628T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080667 | |||||||
chr14:76080680 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0350 |
3 | HG02055.hp1 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-1615A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080680 | |||||||
chr14:76080758 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.296-1537C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080758 | |||||||
chr14:76080794 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-1501A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080794 | |||||||
chr14:76080871 | T | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.296-1424T>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76080871 | |||||||
chr14:76081098 | A | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(11): Show |
15 | HG01928.hp2 HG01943.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.296-1197A>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081098 | |||||||
chr14:76081182 | G | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0058 others(9): Show |
14 | HG01070.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-1113G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081182 | |||||||
chr14:76081198 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1097G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081198 | |||||||
chr14:76081219 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.296-1076G>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081219 | |||||||
chr14:76081326 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.296-969G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081326 | |||||||
chr14:76081338 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0087 |
2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.296-957G>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081338 | |||||||
chr14:76081356 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-939C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081356 | |||||||
chr14:76081393 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.296-902C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081393 | |||||||
chr14:76081481 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.296-814G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081481 | |||||||
chr14:76081541 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-754A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081541 | |||||||
chr14:76081616 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.296-679C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081616 | |||||||
chr14:76081619 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.296-676C>T | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081619 | |||||||
chr14:76081624 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.296-671A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081624 | |||||||
chr14:76081675 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0072 |
3 | HG02895.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.296-620A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081675 | |||||||
chr14:76081704 | A | G | 21 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(18): Show |
22 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.296-591A>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081704 | |||||||
chr14:76081857 | G | A | 16 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0067 others(13): Show |
17 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-438G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081857 | |||||||
chr14:76081933 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-362T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081933 | |||||||
chr14:76081948 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02258.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-347G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76081948 | |||||||
chr14:76082021 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-274G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082021 | |||||||
chr14:76082039 | C | A | 1 | a0001c0001t0001g0320 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-256C>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082039 | |||||||
chr14:76082055 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.296-240C>G | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082055 | |||||||
chr14:76082086 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.296-209A>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 5/8 | chr14 | 76082086 | |||||||
chr14:76082396 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0079 others(6): Show |
12 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.368+29G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | chr14 | 76082396 | |||||||
chr14:76082440 | GGACCTT | G | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.368+76_368+81delCC others(4): Show |
IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr14 | 76082440 | ||||||
chr14:76082510 | T | C | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-107T>C | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 6/8 | chr14 | 76082510 | |||||||
chr14:76082968 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0350 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.445-259G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76082968 | |||||||
chr14:76083011 | G | A | 5 | a0001c0001t0001g0315 a0001c0001t0001g0325 a0001c0001t0001g0326 others(2): Show |
5 | NA18940.hp2 NA18941.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-216G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76083011 | |||||||
chr14:76083034 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(204): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.445-193G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 7/8 | chr14 | 76083034 | |||||||
chr14:76083409 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-49G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/8 | chr14 | 76083409 | |||||||
chr14:76083419 | G | A | 8 | a0001c0001t0001g0083 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-39G>A | IFT43 | ENSG00000119650.13 | transcript | ENST00000314067.11 | protein_coding | 8/8 | chr14 | 76083419 |