Item | Value |
---|---|
geneid | 57560 |
ensemblid | ENSG00000068885.15 |
hgncid | 29262 |
symbol | IFT80 |
name | intraflagellar transport 80 |
refseq_nuc | NM_020800.3 |
refseq_prot | NP_065851.1 |
ensembl_nuc | ENST00000326448.12 |
ensembl_prot | ENSP00000312778.7 |
mane_status | MANE Select |
chr | chr3 |
start | 160256986 |
end | 160399225 |
strand | - |
ver | v1.2 |
region | chr3:160256986-160399225 |
region5000 | chr3:160251986-160404225 |
regionname0 | IFT80_chr3_160256986_160399225 |
regionname5000 | IFT80_chr3_160251986_160404225 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 777 | 120 | 37 | 25 | 30 | 8 | 18 | 23 | IFT80_chr3_160251986_160404225 | IFT80 | MRLKI others(772): Show |
chr3 | 160251986 | 160404225 |
a0002 | 0/0 | 777 | 88 | 51 | 14 | 11 | 4 | 8 | 9 | IFT80_chr3_160251986_160404225 | IFT80 | MRLKI others(772): Show |
chr3 | 160251986 | 160404225 |
a0003 | 0/0 | 777 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | MRLKI others(772): Show |
chr3 | 160251986 | 160404225 |
a0004 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | MRLKI others(772): Show |
chr3 | 160251986 | 160404225 |
a0005 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | MRLKI others(772): Show |
chr3 | 160251986 | 160404225 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2331 | 119 | 37 | 24 | 30 | 8 | 18 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0001c0008 | 0/0 | 2331 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0002c0002 | 0/0 | 2331 | 78 | 44 | 11 | 11 | 4 | 8 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0002c0003 | 0/0 | 2331 | 9 | 6 | 3 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0002c0006 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0003c0004 | 0/0 | 2331 | 2 | 1 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0004c0007 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 | ||
a0005c0005 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | ATGAG others(2326): Show |
chr3 | 160251986 | 160404225 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3999 | 114 | 35 | 24 | 28 | 8 | 17 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0001c0001t0005 | 0/0 | 3999 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0001c0001t0006 | 0/0 | 3999 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0001c0001t0010 | 0/0 | 3999 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0001c0008t0001 | 0/0 | 3999 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0002t0001 | 0/0 | 3999 | 29 | 5 | 7 | 6 | 4 | 7 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0002t0002 | 0/0 | 3999 | 34 | 29 | 4 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0002t0003 | 0/0 | 3999 | 9 | 9 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0002t0004 | 0/0 | 3999 | 5 | 0 | 0 | 5 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0002t0007 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0003t0002 | 0/0 | 3999 | 8 | 5 | 3 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0003t0008 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0002c0006t0002 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0003c0004t0002 | 0/0 | 3999 | 2 | 1 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0004c0007t0001 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
a0005c0005t0009 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | GTAAC others(3994): Show |
chr3 | 160251986 | 160404225 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0001c0008t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0002t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0003t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0002c0006t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0003c0004t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0003c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0004c0007t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
a0005c0005t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0057 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0075 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0072 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0081 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01167 | hp1 | a0002 | c0003 | t0002 | g0080 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01255 | hp2 | a0003 | c0004 | t0002 | g0026 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0079 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01433 | hp1 | a0001 | c0008 | t0001 | g0164 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0074 | EUR | IBS | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0054 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0030 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02523 | hp1 | a0004 | c0007 | t0001 | g0137 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0041 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02630 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02897 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0029 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0205 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02970 | hp2 | a0003 | c0004 | t0002 | g0027 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02976 | hp2 | a0005 | c0005 | t0009 | g0087 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03041 | hp2 | a0002 | c0002 | t0007 | g0088 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03195 | hp1 | a0002 | c0006 | t0002 | g0014 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0036 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03540 | hp1 | a0002 | c0003 | t0002 | g0053 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03579 | hp1 | a0002 | c0003 | t0008 | g0045 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0173 | SAS | PJL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0114 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0052 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | CHB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18960 | hp1 | a0002 | c0002 | t0004 | g0042 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18983 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18990 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19084 | hp2 | a0002 | c0002 | t0004 | g0018 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19088 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ASW | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | GIH | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0038 | AFR | ACB | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | LWK | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0144 | REF | REF | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0155 | REF | REF | IFT80_chr3_160251986_160404225 | IFT80 | chr3 | 160251986 | 160404225 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160277643 | C | T | 1 | a0003 | 2 | HG01255.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1864G>A | p.Ala622Thr | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/20 | 1990/3999 | 1864/2334 | 622/777 | chr3 | 160277643 | |||
chr3:160279273 | T | A | 3 | a0002 a0003 a0005 |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
missense_variant | MODERATE | c.1756A>T | p.Thr586Ser | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/20 | 1882/3999 | 1756/2334 | 586/777 | chr3 | 160279273 | |||
chr3:160280704 | C | T | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1627G>A | p.Asp543Asn | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/20 | 1753/3999 | 1627/2334 | 543/777 | chr3 | 160280704 | |||
chr3:160307663 | G | A | 1 | a0004 | 1 | HG02523.hp1 | missense_variant&splice_region_variant | MODERATE | c.1076C>T | p.Ser359Phe | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/20 | 1202/3999 | 1076/2334 | 359/777 | chr3 | 160307663 | |||
chr3:160319837 | C | T | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.880G>A | p.Val294Ile | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/20 | 1006/3999 | 880/2334 | 294/777 | chr3 | 160319837 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160268497 | A | G | 1 | a0002c0006 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2139T>C | p.Asp713Asp | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/20 | 2265/3999 | 2139/2334 | 713/777 | chr3 | 160268497 | |||
chr3:160366130 | C | T | 1 | a0002c0003 | 9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
synonymous_variant | LOW | c.462G>A | p.Ala154Ala | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/20 | 588/3999 | 462/2334 | 154/777 | chr3 | 160366130 | |||
chr3:160381549 | T | G | 1 | a0001c0008 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.213A>C | p.Val71Val | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/20 | 339/3999 | 213/2334 | 71/777 | chr3 | 160381549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160257271 | G | A | 1 | a0005c0005t0009 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1254 | chr3 | 160257271 | ||||||
chr3:160257321 | C | T | 2 | a0002c0002t0004 a0005c0005t0009 |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1204 | chr3 | 160257321 | ||||||
chr3:160257404 | A | G | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1121T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1121 | chr3 | 160257404 | ||||||
chr3:160257436 | A | G | 1 | a0002c0003t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 1089 | chr3 | 160257436 | ||||||
chr3:160257848 | T | C | 1 | a0001c0001t0006 | 2 | NA18747.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 677 | chr3 | 160257848 | ||||||
chr3:160258271 | A | G | 1 | a0002c0002t0007 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 254 | chr3 | 160258271 | ||||||
chr3:160258343 | A | G | 1 | a0001c0001t0005 | 2 | HG02809.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 182 | chr3 | 160258343 | ||||||
chr3:160258483 | C | T | 9 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0004 others(6): Show |
62 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 20/20 | 42 | chr3 | 160258483 | ||||||
chr3:160384640 | G | A | 1 | a0002c0002t0003 | 9 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/20 | 40 | chr3 | 160384640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160258644 | G | GA | 63 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.2224-10dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258644 | |||||||
chr3:160258644 | GA | G | 7 | a0002c0002t0002g0172 a0002c0002t0002g0173 a0002c0002t0002g0201 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2224-10delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258644 | |||||||
chr3:160258679 | A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-44T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258679 | |||||||
chr3:160258945 | A | G | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2224-310T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160258945 | |||||||
chr3:160259291 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2224-656G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259291 | |||||||
chr3:160259366 | T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2224-731A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259366 | |||||||
chr3:160259729 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-1094A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160259729 | |||||||
chr3:160260091 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2224-1456T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260091 | |||||||
chr3:160260177 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-1542A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260177 | |||||||
chr3:160260320 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2224-1685T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260320 | |||||||
chr3:160260462 | C | T | 4 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0034 others(1): Show |
5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2224-1827G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260462 | |||||||
chr3:160260791 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2224-2156A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260791 | |||||||
chr3:160260891 | T | C | 36 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(33): Show |
39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.2224-2256A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160260891 | |||||||
chr3:160261465 | T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-2830A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261465 | |||||||
chr3:160261474 | C | T | 2 | a0001c0001t0005g0093 a0001c0001t0005g0126 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2224-2839G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261474 | |||||||
chr3:160261685 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2224-3050G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261685 | |||||||
chr3:160261746 | A | G | 60 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(57): Show |
63 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.2224-3111T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261746 | |||||||
chr3:160261801 | C | CA | 31 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(28): Show |
34 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2224-3167dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261801 | |||||||
chr3:160261801 | C | CAA | 5 | a0002c0002t0002g0083 a0002c0002t0003g0030 a0002c0002t0003g0031 others(2): Show |
5 | HG02451.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2224-3168_2224-316 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160261801 | |||||||
chr3:160262032 | T | C | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2224-3397A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262032 | |||||||
chr3:160262061 | G | A | 1 | a0002c0002t0001g0086 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2224-3426C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262061 | |||||||
chr3:160262169 | C | G | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2224-3534G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262169 | |||||||
chr3:160262324 | G | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2224-3689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262324 | |||||||
chr3:160262482 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.2224-3847C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262482 | |||||||
chr3:160262495 | A | AT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.2224-3861dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262495 | |||||||
chr3:160262596 | A | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2224-3961T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262596 | |||||||
chr3:160262617 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2224-3982C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262617 | |||||||
chr3:160262666 | T | C | 1 | a0003c0004t0002g0027 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2224-4031A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262666 | |||||||
chr3:160262778 | A | G | 7 | a0001c0001t0001g0092 a0001c0001t0001g0174 a0001c0001t0001g0176 others(4): Show |
7 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2224-4143T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262778 | |||||||
chr3:160262822 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2224-4187G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262822 | |||||||
chr3:160262876 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2224-4241T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262876 | |||||||
chr3:160262964 | C | T | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2224-4329G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160262964 | |||||||
chr3:160263002 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2224-4367A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263002 | |||||||
chr3:160263059 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0183 |
2 | HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2224-4424G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263059 | |||||||
chr3:160263133 | T | C | 20 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(17): Show |
21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.2224-4498A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263133 | |||||||
chr3:160263365 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2224-4730G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263365 | |||||||
chr3:160263399 | T | C | 2 | a0001c0001t0005g0093 a0001c0001t0005g0126 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2224-4764A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263399 | |||||||
chr3:160263428 | C | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2224-4793G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263428 | |||||||
chr3:160263464 | C | T | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2224-4829G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263464 | |||||||
chr3:160263494 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2224-4859G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263494 | |||||||
chr3:160263892 | C | T | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2223+4521G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160263892 | |||||||
chr3:160264086 | G | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2223+4327C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264086 | |||||||
chr3:160264599 | CT | C | 53 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(50): Show |
56 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(53): Show |
intron_variant | MODIFIER | c.2223+3813delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264599 | |||||||
chr3:160264719 | T | C | 60 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(57): Show |
63 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.2223+3694A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160264719 | |||||||
chr3:160265044 | A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2223+3369T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265044 | |||||||
chr3:160265627 | T | C | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2223+2786A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265627 | |||||||
chr3:160265703 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0025 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2223+2710C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265703 | |||||||
chr3:160265941 | G | A | 16 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(13): Show |
18 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.2223+2472C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160265941 | |||||||
chr3:160266082 | A | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2223+2331T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266082 | |||||||
chr3:160266283 | T | A | 7 | a0002c0002t0002g0172 a0002c0002t0002g0173 a0002c0002t0002g0201 others(4): Show |
7 | HG02258.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2223+2130A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266283 | |||||||
chr3:160266313 | T | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2223+2100A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266313 | |||||||
chr3:160266339 | TC | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0092 others(71): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.2223+2073delG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266339 | |||||||
chr3:160266566 | T | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2223+1847A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266566 | |||||||
chr3:160266822 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2223+1591A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266822 | |||||||
chr3:160266971 | T | G | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223+1442A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160266971 | |||||||
chr3:160267208 | T | C | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223+1205A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267208 | |||||||
chr3:160267219 | C | T | 22 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(19): Show |
22 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.2223+1194G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267219 | |||||||
chr3:160267353 | A | T | 16 | a0002c0002t0002g0172 a0002c0002t0002g0173 a0002c0002t0002g0201 others(13): Show |
16 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.2223+1060T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267353 | |||||||
chr3:160267387 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2223+1026A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267387 | |||||||
chr3:160267387 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2223+1026A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267387 | |||||||
chr3:160267737 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2223+676A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267737 | |||||||
chr3:160267919 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2223+494C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160267919 | |||||||
chr3:160268097 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2223+316C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268097 | |||||||
chr3:160268360 | G | A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01243.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2223+53C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268360 | |||||||
chr3:160268377 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2223+36G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 19/19 | chr3 | 160268377 | |||||||
chr3:160268642 | T | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2100-106A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160268642 | |||||||
chr3:160269222 | CA | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(57): Show |
63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.2100-687delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269222 | |||||||
chr3:160269222 | CAA | C | 44 | a0002c0002t0002g0004 a0002c0002t0002g0015 a0002c0002t0002g0021 others(41): Show |
45 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.2100-688_2100-687d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269222 | |||||||
chr3:160269600 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2100-1064A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160269600 | |||||||
chr3:160270050 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2100-1514C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160270050 | |||||||
chr3:160270197 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2100-1661G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160270197 | |||||||
chr3:160271016 | TATG | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2483_2100-248 others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271016 | |||||||
chr3:160271568 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2100-3032G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271568 | |||||||
chr3:160271941 | CA | C | 25 | a0001c0001t0001g0106 a0002c0002t0001g0046 a0002c0002t0001g0047 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2100-3406delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271941 | |||||||
chr3:160271960 | A | G | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2100-3424T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160271960 | |||||||
chr3:160272043 | G | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2100-3507C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272043 | |||||||
chr3:160272531 | T | A | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2100-3995A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272531 | |||||||
chr3:160272560 | C | T | 36 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(33): Show |
39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.2100-4024G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272560 | |||||||
chr3:160272688 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2100-4152G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272688 | |||||||
chr3:160272737 | T | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0082 |
2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2100-4201A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272737 | |||||||
chr3:160272854 | A | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2100-4318T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160272854 | |||||||
chr3:160273051 | C | T | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099+4255G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273051 | |||||||
chr3:160273087 | T | C | 1 | a0002c0002t0002g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2099+4219A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273087 | |||||||
chr3:160273222 | A | G | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2099+4084T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273222 | |||||||
chr3:160273326 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2099+3980G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273326 | |||||||
chr3:160273394 | G | GTAGAT | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2099+3907_2099+391 others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273394 | |||||||
chr3:160273636 | A | T | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2099+3670T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273636 | |||||||
chr3:160273682 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2099+3624A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273682 | |||||||
chr3:160273724 | A | G | 69 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
72 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.2099+3582T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273724 | |||||||
chr3:160273832 | T | G | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2099+3474A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273832 | |||||||
chr3:160273865 | G | A | 4 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0034 others(1): Show |
5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2099+3441C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160273865 | |||||||
chr3:160274022 | T | C | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2099+3284A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274022 | |||||||
chr3:160274256 | T | C | 1 | a0002c0002t0002g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2099+3050A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274256 | |||||||
chr3:160274677 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2099+2629C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274677 | |||||||
chr3:160274768 | G | A | 25 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2099+2538C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274768 | |||||||
chr3:160274856 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2099+2450C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274856 | |||||||
chr3:160274927 | C | A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2099+2379G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274927 | |||||||
chr3:160274961 | T | A | 4 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0204 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2099+2345A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274961 | |||||||
chr3:160274961 | T | C | 2 | a0002c0002t0004g0042 a0002c0002t0004g0043 |
2 | NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2099+2345A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160274961 | |||||||
chr3:160275119 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2099+2187A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275119 | |||||||
chr3:160275223 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2099+2083A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275223 | |||||||
chr3:160275329 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2099+1977C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275329 | |||||||
chr3:160275342 | T | G | 9 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(6): Show |
9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2099+1964A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275342 | |||||||
chr3:160275424 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2099+1882A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275424 | |||||||
chr3:160275647 | T | A | 88 | a0002c0002t0001g0033 a0002c0002t0001g0046 a0002c0002t0001g0047 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+1659A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275647 | |||||||
chr3:160275702 | C | T | 88 | a0002c0002t0001g0033 a0002c0002t0001g0046 a0002c0002t0001g0047 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+1604G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275702 | |||||||
chr3:160275735 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2099+1571T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275735 | |||||||
chr3:160275784 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG00099.hp2 HG00323.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2099+1522T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275784 | |||||||
chr3:160275787 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2099+1519C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275787 | |||||||
chr3:160275794 | AT | A | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2099+1511delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275794 | |||||||
chr3:160275804 | A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2099+1502T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275804 | |||||||
chr3:160275987 | C | A | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2099+1319G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160275987 | |||||||
chr3:160276160 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2099+1146C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276160 | |||||||
chr3:160276228 | A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2099+1078T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276228 | |||||||
chr3:160276799 | T | C | 25 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2099+507A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276799 | |||||||
chr3:160276975 | T | C | 24 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.2099+331A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276975 | |||||||
chr3:160276984 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2099+322A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160276984 | |||||||
chr3:160277157 | T | C | 88 | a0002c0002t0001g0033 a0002c0002t0001g0046 a0002c0002t0001g0047 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2099+149A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 18/19 | chr3 | 160277157 | |||||||
chr3:160277511 | A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1927-33T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/19 | chr3 | 160277511 | |||||||
chr3:160277568 | A | G | 37 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1926+13T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 17/19 | chr3 | 160277568 | |||||||
chr3:160277744 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1837-74G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160277744 | |||||||
chr3:160277996 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1837-326T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160277996 | |||||||
chr3:160278027 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1837-357C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278027 | |||||||
chr3:160278204 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1837-534C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278204 | |||||||
chr3:160278334 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1837-664A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278334 | |||||||
chr3:160278441 | T | C | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1836+752A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278441 | |||||||
chr3:160278531 | C | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1836+662G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160278531 | |||||||
chr3:160279069 | TA | T | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1836+123delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160279069 | |||||||
chr3:160279138 | AAAGGTAA others(3): Show |
A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1836+45_1836+54del others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 16/19 | chr3 | 160279138 | |||||||
chr3:160279676 | C | CCT | 105 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1665-313_1665-312i others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160279676 | |||||||
chr3:160279759 | C | T | 88 | a0002c0002t0001g0033 a0002c0002t0001g0046 a0002c0002t0001g0047 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1665-395G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160279759 | |||||||
chr3:160280323 | C | A | 1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1664+344G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280323 | |||||||
chr3:160280390 | TG | T | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1664+276delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280390 | |||||||
chr3:160280440 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1664+227C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280440 | |||||||
chr3:160280453 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1664+214T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280453 | |||||||
chr3:160280583 | A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1664+84T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280583 | |||||||
chr3:160280594 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1664+73A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 15/19 | chr3 | 160280594 | |||||||
chr3:160281030 | C | T | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1517-216G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281030 | |||||||
chr3:160281564 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1517-750G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281564 | |||||||
chr3:160281656 | T | C | 3 | a0002c0002t0001g0057 a0002c0002t0001g0084 a0002c0002t0001g0085 |
3 | HG00099.hp1 HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1516+822A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160281656 | |||||||
chr3:160282271 | C | A | 2 | a0002c0002t0004g0042 a0002c0002t0004g0043 |
2 | NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1516+207G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282271 | |||||||
chr3:160282369 | A | G | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1516+109T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282369 | |||||||
chr3:160282376 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1516+102C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282376 | |||||||
chr3:160282430 | A | G | 6 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0062 others(3): Show |
6 | HG00423.hp2 HG00558.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1516+48T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282430 | |||||||
chr3:160282441 | G | A | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516+37C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 14/19 | chr3 | 160282441 | |||||||
chr3:160283081 | A | G | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381-468T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283081 | |||||||
chr3:160283111 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1381-498A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283111 | |||||||
chr3:160283233 | A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1381-620T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283233 | |||||||
chr3:160283274 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1381-661A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283274 | |||||||
chr3:160283334 | C | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0046 a0002c0002t0001g0047 others(84): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1381-721G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283334 | |||||||
chr3:160283578 | A | G | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1381-965T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283578 | |||||||
chr3:160283688 | C | G | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1381-1075G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283688 | |||||||
chr3:160283869 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1381-1256A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160283869 | |||||||
chr3:160284072 | C | G | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-1459G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284072 | |||||||
chr3:160284140 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1381-1527A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284140 | |||||||
chr3:160284141 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1381-1528C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284141 | |||||||
chr3:160284446 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1380+1358C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284446 | |||||||
chr3:160284678 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1380+1126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284678 | |||||||
chr3:160284774 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0135 |
2 | HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1380+1030G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284774 | |||||||
chr3:160284780 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0135 |
2 | HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1380+1024G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284780 | |||||||
chr3:160284821 | T | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG02293.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1380+983A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284821 | |||||||
chr3:160284854 | A | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+950T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160284854 | |||||||
chr3:160285067 | G | C | 2 | a0002c0002t0002g0015 a0002c0002t0007g0088 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1380+737C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285067 | |||||||
chr3:160285151 | C | T | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1380+653G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285151 | |||||||
chr3:160285660 | G | A | 36 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(33): Show |
39 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1380+144C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 13/19 | chr3 | 160285660 | |||||||
chr3:160285889 | T | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(31): Show |
35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1316-21A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160285889 | |||||||
chr3:160286111 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1316-243G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286111 | |||||||
chr3:160286238 | A | G | 129 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1316-370T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286238 | |||||||
chr3:160286251 | T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1316-383A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286251 | |||||||
chr3:160286419 | C | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-551G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286419 | |||||||
chr3:160286573 | T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-705A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286573 | |||||||
chr3:160286580 | A | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1316-712T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286580 | |||||||
chr3:160286831 | A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-963T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160286831 | |||||||
chr3:160287258 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-1390A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287258 | |||||||
chr3:160287269 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-1401G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287269 | |||||||
chr3:160287486 | T | C | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1316-1618A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287486 | |||||||
chr3:160287545 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1316-1677C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287545 | |||||||
chr3:160287912 | G | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1316-2044C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160287912 | |||||||
chr3:160288070 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1316-2202G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288070 | |||||||
chr3:160288111 | G | A | 9 | a0002c0002t0002g0015 a0002c0002t0002g0172 a0002c0002t0002g0173 others(6): Show |
9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316-2243C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288111 | |||||||
chr3:160288563 | T | C | 45 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1316-2695A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288563 | |||||||
chr3:160288584 | T | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-2716A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160288584 | |||||||
chr3:160289433 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-3565G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289433 | |||||||
chr3:160289437 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1316-3569A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289437 | |||||||
chr3:160289557 | C | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-3689G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289557 | |||||||
chr3:160289609 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1316-3741G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289609 | |||||||
chr3:160289612 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1316-3744G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289612 | |||||||
chr3:160289746 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1316-3878A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160289746 | |||||||
chr3:160290136 | C | T | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-4268G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290136 | |||||||
chr3:160290332 | T | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316-4464A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290332 | |||||||
chr3:160290352 | G | T | 16 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(13): Show |
18 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1316-4484C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290352 | |||||||
chr3:160290394 | C | T | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-4526G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290394 | |||||||
chr3:160290411 | CAGAAAAA others(5): Show |
C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316-4555_1316-454 others(16): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290411 | |||||||
chr3:160290535 | G | A | 2 | a0001c0001t0006g0198 a0002c0002t0002g0083 |
2 | HG02615.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1316-4667C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290535 | |||||||
chr3:160290761 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1316-4893G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160290761 | |||||||
chr3:160291498 | A | G | 1 | a0002c0002t0003g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1316-5630T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291498 | |||||||
chr3:160291632 | G | A | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1316-5764C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291632 | |||||||
chr3:160291642 | C | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1316-5774G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291642 | |||||||
chr3:160291695 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1316-5827A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291695 | |||||||
chr3:160291744 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1316-5876A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291744 | |||||||
chr3:160291848 | A | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-5980T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291848 | |||||||
chr3:160291953 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1316-6085T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160291953 | |||||||
chr3:160292124 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1316-6256G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292124 | |||||||
chr3:160292254 | C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316-6386G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292254 | |||||||
chr3:160292260 | A | G | 1 | a0002c0002t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1316-6392T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292260 | |||||||
chr3:160292338 | A | G | 1 | a0002c0002t0004g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1316-6470T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292338 | |||||||
chr3:160292451 | T | C | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1316-6583A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292451 | |||||||
chr3:160292475 | C | CT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG00423.hp1 HG00735.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316-6608dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292475 | |||||||
chr3:160292475 | CT | C | 74 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0191 others(71): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1316-6608delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292475 | |||||||
chr3:160292694 | G | T | 1 | a0003c0004t0002g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1316-6826C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292694 | |||||||
chr3:160292728 | G | A | 6 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(3): Show |
7 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316-6860C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160292728 | |||||||
chr3:160293124 | A | G | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1316-7256T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293124 | |||||||
chr3:160293351 | T | C | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1316-7483A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293351 | |||||||
chr3:160293516 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG01243.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+7367A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293516 | |||||||
chr3:160293614 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1315+7269G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293614 | |||||||
chr3:160293688 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1315+7195A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160293688 | |||||||
chr3:160294210 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1315+6673A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294210 | |||||||
chr3:160294280 | G | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1315+6603C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294280 | |||||||
chr3:160294533 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02257.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1315+6350G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294533 | |||||||
chr3:160294551 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1315+6332A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294551 | |||||||
chr3:160294887 | GTGCAGTC | G | 3 | a0002c0002t0001g0047 a0002c0002t0001g0066 a0002c0002t0001g0067 |
3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1315+5989_1315+599 others(11): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160294887 | |||||||
chr3:160295021 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1315+5862C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295021 | |||||||
chr3:160295099 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1315+5784C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295099 | |||||||
chr3:160295423 | A | AGTGAGCC others(3): Show |
2 | a0002c0002t0002g0048 a0002c0002t0002g0082 |
2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1315+5450_1315+545 others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295423 | |||||||
chr3:160295544 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1315+5339G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295544 | |||||||
chr3:160295569 | A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1315+5314T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295569 | |||||||
chr3:160295736 | A | C | 1 | a0002c0002t0003g0002 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1315+5147T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295736 | |||||||
chr3:160295742 | A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1315+5141T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295742 | |||||||
chr3:160295981 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1315+4902G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160295981 | |||||||
chr3:160296344 | A | G | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1315+4539T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296344 | |||||||
chr3:160296542 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+4341A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296542 | |||||||
chr3:160296611 | T | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+4272A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296611 | |||||||
chr3:160296649 | T | G | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1315+4234A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160296649 | |||||||
chr3:160297080 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1315+3803A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297080 | |||||||
chr3:160297115 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1315+3768T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297115 | |||||||
chr3:160297116 | T | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0119 others(5): Show |
8 | HG00323.hp1 HG01358.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315+3767A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297116 | |||||||
chr3:160297179 | C | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1315+3704G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297179 | |||||||
chr3:160297575 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+3308C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297575 | |||||||
chr3:160297589 | C | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+3294G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297589 | |||||||
chr3:160297833 | G | A | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315+3050C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297833 | |||||||
chr3:160297857 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1315+3026A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297857 | |||||||
chr3:160297969 | G | A | 2 | a0002c0002t0003g0030 a0002c0002t0003g0031 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1315+2914C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160297969 | |||||||
chr3:160298061 | C | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+2822G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298061 | |||||||
chr3:160298106 | G | A | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1315+2777C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298106 | |||||||
chr3:160298147 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1315+2736T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298147 | |||||||
chr3:160298156 | A | G | 1 | a0004c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1315+2727T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298156 | |||||||
chr3:160298339 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1315+2544T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298339 | |||||||
chr3:160298350 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1315+2533G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298350 | |||||||
chr3:160298412 | CAG | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+2469_1315+247 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298412 | |||||||
chr3:160298578 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1315+2305A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298578 | |||||||
chr3:160298584 | CCAGAAAA others(3): Show |
C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1315+2289_1315+229 others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298584 | |||||||
chr3:160298658 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1315+2225A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160298658 | |||||||
chr3:160299082 | C | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1315+1801G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299082 | |||||||
chr3:160299198 | A | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+1685T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299198 | |||||||
chr3:160299510 | T | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0134 a0001c0001t0001g0136 others(2): Show |
5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315+1373A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299510 | |||||||
chr3:160299681 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1315+1202A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299681 | |||||||
chr3:160299954 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1315+929G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160299954 | |||||||
chr3:160300061 | C | G | 2 | a0002c0002t0002g0004 a0002c0002t0002g0028 |
3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1315+822G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300061 | |||||||
chr3:160300146 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1315+737G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300146 | |||||||
chr3:160300166 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+717A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300166 | |||||||
chr3:160300335 | C | T | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+548G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300335 | |||||||
chr3:160300486 | T | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315+397A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300486 | |||||||
chr3:160300736 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+147A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300736 | |||||||
chr3:160300823 | A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1315+60T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300823 | |||||||
chr3:160300854 | G | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315+29C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 12/19 | chr3 | 160300854 | |||||||
chr3:160301074 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1152-28G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301074 | |||||||
chr3:160301172 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1152-126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301172 | |||||||
chr3:160301348 | C | A | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152-302G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301348 | |||||||
chr3:160301511 | A | G | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152-465T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301511 | |||||||
chr3:160301653 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1152-607T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301653 | |||||||
chr3:160301753 | T | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1152-707A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301753 | |||||||
chr3:160301760 | T | G | 2 | a0003c0004t0002g0026 a0003c0004t0002g0027 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1152-714A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301760 | |||||||
chr3:160301777 | A | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152-731T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160301777 | |||||||
chr3:160302081 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152-1035A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302081 | |||||||
chr3:160302292 | C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1152-1246G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302292 | |||||||
chr3:160302709 | G | A | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1151+1206C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302709 | |||||||
chr3:160302711 | T | C | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1151+1204A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302711 | |||||||
chr3:160302720 | T | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151+1195A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302720 | |||||||
chr3:160302761 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1151+1154A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302761 | |||||||
chr3:160302925 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151+990G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302925 | |||||||
chr3:160302991 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151+924C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160302991 | |||||||
chr3:160303090 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1151+825G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303090 | |||||||
chr3:160303318 | G | C | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1151+597C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303318 | |||||||
chr3:160303363 | G | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151+552C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303363 | |||||||
chr3:160303520 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1151+395C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303520 | |||||||
chr3:160303726 | T | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG01243.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151+189A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303726 | |||||||
chr3:160303893 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1151+22C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 11/19 | chr3 | 160303893 | |||||||
chr3:160304194 | C | T | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077-205G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304194 | |||||||
chr3:160304340 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1077-351C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304340 | |||||||
chr3:160304435 | C | CT | 38 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0146 others(35): Show |
38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1077-447dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304435 | |||||||
chr3:160304616 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1077-627A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304616 | |||||||
chr3:160304809 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1077-820A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304809 | |||||||
chr3:160304812 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0147 |
3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1077-823A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304812 | |||||||
chr3:160304833 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1077-844A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160304833 | |||||||
chr3:160305035 | C | T | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1077-1046G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305035 | |||||||
chr3:160305108 | C | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1077-1119G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305108 | |||||||
chr3:160305202 | C | A | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1077-1213G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305202 | |||||||
chr3:160305208 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-1219G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305208 | |||||||
chr3:160305532 | G | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(29): Show |
33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1077-1543C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305532 | |||||||
chr3:160305695 | T | C | 1 | a0002c0002t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1077-1706A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305695 | |||||||
chr3:160305757 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1077-1768A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305757 | |||||||
chr3:160305968 | T | C | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1076+1695A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160305968 | |||||||
chr3:160306062 | A | G | 8 | a0002c0002t0003g0002 a0002c0002t0003g0029 a0002c0002t0003g0030 others(5): Show |
9 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076+1601T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306062 | |||||||
chr3:160306393 | A | G | 1 | a0002c0002t0002g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1076+1270T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306393 | |||||||
chr3:160306425 | T | C | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1076+1238A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306425 | |||||||
chr3:160306494 | A | G | 2 | a0002c0002t0002g0004 a0002c0002t0002g0028 |
3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1076+1169T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306494 | |||||||
chr3:160306499 | C | A | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1076+1164G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306499 | |||||||
chr3:160306586 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1076+1077T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306586 | |||||||
chr3:160306594 | A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1076+1069T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306594 | |||||||
chr3:160306726 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+937C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306726 | |||||||
chr3:160306997 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1076+666A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160306997 | |||||||
chr3:160307263 | C | A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1076+400G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307263 | |||||||
chr3:160307359 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1076+304A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307359 | |||||||
chr3:160307445 | C | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1076+218G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307445 | |||||||
chr3:160307450 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1076+213C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307450 | |||||||
chr3:160307454 | A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076+209T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307454 | |||||||
chr3:160307499 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1076+164G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307499 | |||||||
chr3:160307622 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1076+41G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307622 | |||||||
chr3:160307654 | G | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1076+9C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 10/19 | chr3 | 160307654 | |||||||
chr3:160307844 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-63C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160307844 | |||||||
chr3:160307849 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.958-68G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160307849 | |||||||
chr3:160308275 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.958-494T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308275 | |||||||
chr3:160308291 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.958-510C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308291 | |||||||
chr3:160308366 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.958-585C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308366 | |||||||
chr3:160308647 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-866A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308647 | |||||||
chr3:160308837 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-1056C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308837 | |||||||
chr3:160308842 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-1061A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160308842 | |||||||
chr3:160309171 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-1390G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309171 | |||||||
chr3:160309232 | G | A | 1 | a0002c0002t0002g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.958-1451C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309232 | |||||||
chr3:160309569 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-1788G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309569 | |||||||
chr3:160309637 | A | T | 1 | a0004c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.958-1856T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309637 | |||||||
chr3:160309729 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.958-1948A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309729 | |||||||
chr3:160309995 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-2214C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160309995 | |||||||
chr3:160310041 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-2260G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310041 | |||||||
chr3:160310226 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.958-2445A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310226 | |||||||
chr3:160310368 | A | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.958-2587T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310368 | |||||||
chr3:160310430 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.958-2649C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310430 | |||||||
chr3:160310460 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-2679T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310460 | |||||||
chr3:160310659 | CTA | C | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.958-2880_958-2879d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310659 | |||||||
chr3:160310685 | A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.958-2904T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310685 | |||||||
chr3:160310773 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-2992C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310773 | |||||||
chr3:160310844 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.958-3063A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160310844 | |||||||
chr3:160311017 | C | G | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-3236G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311017 | |||||||
chr3:160311134 | A | C | 20 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(17): Show |
21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.958-3353T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311134 | |||||||
chr3:160311187 | G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-3406C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311187 | |||||||
chr3:160311344 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.958-3563T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311344 | |||||||
chr3:160311376 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.958-3595A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311376 | |||||||
chr3:160311464 | T | C | 1 | a0005c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.958-3683A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311464 | |||||||
chr3:160311533 | G | A | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.958-3752C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311533 | |||||||
chr3:160311662 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-3881T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311662 | |||||||
chr3:160311893 | G | A | 1 | a0002c0002t0002g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.958-4112C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160311893 | |||||||
chr3:160312169 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.958-4388A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312169 | |||||||
chr3:160312176 | G | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.958-4395C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312176 | |||||||
chr3:160312355 | C | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-4574G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312355 | |||||||
chr3:160312372 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.958-4591T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312372 | |||||||
chr3:160312542 | T | C | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.958-4761A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312542 | |||||||
chr3:160312576 | T | TATATATA others(30): Show |
1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.958-4832_958-4796d others(39): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312576 | |||||||
chr3:160312583 | A | AATATATA others(34): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0147 |
3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.958-4843_958-4803d others(43): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312583 | |||||||
chr3:160312596 | A | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.958-4815T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312596 | |||||||
chr3:160312610 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4829T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312610 | |||||||
chr3:160312611 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4830A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312611 | |||||||
chr3:160312612 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-4831T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312612 | |||||||
chr3:160312620 | AAT | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0113 a0001c0001t0001g0116 others(47): Show |
53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.958-4841_958-4840d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312620 | |||||||
chr3:160312622 | TATATATA others(39): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.958-4887_958-4842d others(48): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312622 | |||||||
chr3:160312624 | TATATATA others(37): Show |
T | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.958-4887_958-4844d others(46): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312624 | |||||||
chr3:160312663 | TATATA | T | 4 | a0002c0002t0003g0031 a0002c0003t0002g0079 a0002c0003t0002g0080 others(1): Show |
4 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-4887_958-4883d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312663 | |||||||
chr3:160312665 | TATA | T | 2 | a0001c0001t0001g0153 a0002c0002t0002g0201 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.958-4887_958-4885d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312665 | |||||||
chr3:160312674 | T | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0100 a0001c0001t0001g0101 others(14): Show |
18 | HG00323.hp1 HG01358.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.958-4893A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312674 | |||||||
chr3:160312705 | AATATATA others(39): Show |
A | 2 | a0002c0002t0002g0048 a0002c0002t0002g0082 |
2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.958-4970_958-4925d others(48): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312705 | |||||||
chr3:160312711 | TAATATAT others(3): Show |
T | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.958-4940_958-4931d others(12): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312711 | |||||||
chr3:160312712 | A | ATATAAAT others(24): Show |
1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-4932_958-4931i others(33): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312712 | |||||||
chr3:160312712 | AATATATA others(1): Show |
A | 6 | a0002c0002t0002g0055 a0002c0002t0002g0083 a0002c0003t0002g0079 others(3): Show |
6 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-4939_958-4932d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312712 | |||||||
chr3:160312721 | A | T | 6 | a0002c0002t0002g0055 a0002c0002t0002g0083 a0002c0003t0002g0079 others(3): Show |
6 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-4940T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312721 | |||||||
chr3:160312728 | A | G | 22 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0015 others(19): Show |
24 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.958-4947T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312728 | |||||||
chr3:160312757 | T | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-4976A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | |||||||
chr3:160312757 | T | TA | 5 | a0002c0002t0002g0015 a0002c0003t0002g0079 a0002c0003t0002g0080 others(2): Show |
5 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-4977dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | |||||||
chr3:160312757 | T | TATA | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.958-4979_958-4977d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | |||||||
chr3:160312757 | T | TATAAATG others(32): Show |
11 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(8): Show |
11 | HG01433.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.958-5015_958-4977d others(41): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | |||||||
chr3:160312757 | T | TATAATAA others(35): Show |
1 | a0001c0001t0005g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.958-4977_958-4976i others(44): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312757 | |||||||
chr3:160312759 | T | A | 27 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.958-4978A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312759 | |||||||
chr3:160312764 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-4983C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312764 | |||||||
chr3:160312769 | T | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-4988A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312769 | |||||||
chr3:160312785 | AAT | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.958-5006_958-5005d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312785 | |||||||
chr3:160312785 | AATAT | A | 2 | a0001c0001t0001g0143 a0002c0002t0002g0015 |
2 | HG02486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.958-5008_958-5005d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312785 | |||||||
chr3:160312786 | ATATATAT others(15): Show |
A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.958-5027_958-5006d others(24): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312786 | |||||||
chr3:160312788 | A | ATATATAA others(10): Show |
1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.958-5008_958-5007i others(19): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312788 | |||||||
chr3:160312803 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-5022C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312803 | |||||||
chr3:160312824 | AAT | A | 7 | a0002c0002t0002g0015 a0002c0003t0002g0050 a0002c0003t0002g0051 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5045_958-5044d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312824 | |||||||
chr3:160312824 | AATAT | A | 18 | a0001c0001t0001g0143 a0002c0002t0001g0033 a0002c0002t0002g0003 others(15): Show |
19 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.958-5047_958-5044d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312824 | |||||||
chr3:160312827 | A | ATATAATA others(59): Show |
2 | a0002c0002t0003g0002 a0002c0002t0003g0040 |
3 | HG02895.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.958-5047_958-5046i others(68): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312827 | |||||||
chr3:160312828 | T | TATAATAA others(59): Show |
1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-5048_958-5047i others(68): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312828 | |||||||
chr3:160312828 | T | TATATATA others(106): Show |
1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.958-5048_958-5047i others(115): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312828 | |||||||
chr3:160312832 | TATA | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(35): Show |
39 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.958-5054_958-5052d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312832 | |||||||
chr3:160312842 | G | A | 19 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0015 others(16): Show |
21 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.958-5061C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | |||||||
chr3:160312842 | G | GTATATTA others(28): Show |
2 | a0001c0001t0001g0130 a0002c0002t0007g0088 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.958-5096_958-5062d others(37): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | |||||||
chr3:160312842 | GTATATTA others(28): Show |
G | 2 | a0001c0001t0001g0150 a0001c0001t0010g0114 |
2 | HG01069.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.958-5096_958-5062d others(37): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312842 | |||||||
chr3:160312863 | A | AAT | 6 | a0002c0002t0002g0083 a0002c0002t0003g0002 a0002c0002t0003g0040 others(3): Show |
7 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5084_958-5083d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | |||||||
chr3:160312863 | A | AATAT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.958-5086_958-5083d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | |||||||
chr3:160312863 | A | T | 1 | a0002c0002t0002g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.958-5082T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312863 | |||||||
chr3:160312877 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0161 others(3): Show |
7 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5096T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312877 | |||||||
chr3:160312890 | A | AAATATAT others(70): Show |
1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.958-5186_958-5110d others(79): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312890 | |||||||
chr3:160312898 | A | AAT | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.958-5119_958-5118d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312898 | |||||||
chr3:160312906 | A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5125T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312906 | |||||||
chr3:160312907 | T | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5126A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312907 | |||||||
chr3:160312909 | A | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.958-5128T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312909 | |||||||
chr3:160312925 | A | AAATATAT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(64): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.958-5151_958-5145d others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | |||||||
chr3:160312925 | A | AAATATAT others(35): Show |
1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.958-5186_958-5145d others(44): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | |||||||
chr3:160312925 | A | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.958-5144T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312925 | |||||||
chr3:160312933 | A | AAT | 15 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(12): Show |
15 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-5154_958-5153d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312933 | |||||||
chr3:160312933 | A | T | 7 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(4): Show |
8 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-5152T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312933 | |||||||
chr3:160312935 | TATATAAT others(2): Show |
T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5163_958-5155d others(11): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312935 | |||||||
chr3:160312941 | A | T | 19 | a0002c0002t0002g0004 a0002c0002t0002g0022 a0002c0002t0002g0023 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5160T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312941 | |||||||
chr3:160312942 | T | A | 19 | a0002c0002t0002g0004 a0002c0002t0002g0022 a0002c0002t0002g0023 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5161A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312942 | |||||||
chr3:160312942 | TAA | T | 3 | a0002c0002t0002g0035 a0002c0002t0003g0002 a0002c0002t0003g0040 |
4 | HG01243.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5163_958-5162d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312942 | |||||||
chr3:160312943 | A | T | 2 | a0002c0002t0002g0021 a0002c0002t0002g0044 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.958-5162T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312943 | |||||||
chr3:160312944 | A | AATATATA others(170): Show |
1 | a0002c0002t0003g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.958-5164_958-5163i others(179): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | |||||||
chr3:160312944 | A | AATATATA others(100): Show |
7 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(4): Show |
8 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-5164_958-5163i others(109): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | |||||||
chr3:160312944 | A | AATATATA others(135): Show |
4 | a0002c0002t0003g0029 a0002c0002t0003g0030 a0002c0002t0003g0039 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5164_958-5163i others(144): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | |||||||
chr3:160312944 | A | T | 19 | a0002c0002t0002g0004 a0002c0002t0002g0022 a0002c0002t0002g0023 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.958-5163T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312944 | |||||||
chr3:160312951 | AT | A | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.958-5171delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312951 | |||||||
chr3:160312960 | AAATATAT | A | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-5186_958-5180d others(9): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312960 | |||||||
chr3:160312967 | T | TAATATAT others(21): Show |
1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.958-5187_958-5186i others(30): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312967 | |||||||
chr3:160312986 | A | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0002c0002t0002g0028 |
3 | HG01106.hp1 HG01168.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.958-5205T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312986 | |||||||
chr3:160312986 | AAT | A | 4 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0204 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-5207_958-5206d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160312986 | |||||||
chr3:160313051 | TA | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.958-5271delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313051 | |||||||
chr3:160313148 | C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.958-5367G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313148 | |||||||
chr3:160313608 | A | AT | 7 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0121 others(4): Show |
7 | HG01106.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-5828dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313608 | |||||||
chr3:160313657 | T | C | 37 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.958-5876A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313657 | |||||||
chr3:160313854 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0145 |
3 | HG02818.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.957+5906G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160313854 | |||||||
chr3:160314035 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.957+5725T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314035 | |||||||
chr3:160314190 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.957+5570G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314190 | |||||||
chr3:160314198 | G | A | 25 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.957+5562C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314198 | |||||||
chr3:160314228 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.957+5532A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314228 | |||||||
chr3:160314453 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG00099.hp2 HG03834.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+5307G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314453 | |||||||
chr3:160314493 | G | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+5267C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314493 | |||||||
chr3:160314566 | A | G | 1 | a0002c0002t0002g0004 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.957+5194T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314566 | |||||||
chr3:160314596 | C | T | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.957+5164G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314596 | |||||||
chr3:160314599 | G | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+5161C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314599 | |||||||
chr3:160314681 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.957+5079A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314681 | |||||||
chr3:160314750 | C | T | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.957+5010G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314750 | |||||||
chr3:160314755 | C | T | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.957+5005G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160314755 | |||||||
chr3:160315053 | A | AAGGG | 33 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0091 others(30): Show |
35 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.957+4703_957+4706d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | A | AAGGGAGG others(1): Show |
19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(16): Show |
20 | HG00558.hp1 HG01069.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.957+4699_957+4706d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | A | AAGGGAGG others(5): Show |
56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(53): Show |
57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.957+4695_957+4706d others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | A | AAGGGAGG others(9): Show |
6 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0185 others(3): Show |
6 | HG02055.hp2 HG02922.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.957+4691_957+4706d others(18): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | A | AAGGGAGG others(13): Show |
2 | a0001c0001t0006g0198 a0002c0002t0002g0049 |
2 | HG02717.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+4687_957+4706d others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | AAGGG | A | 24 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0161 others(21): Show |
26 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.957+4703_957+4706d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | AAGGGAGG others(1): Show |
A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0134 others(52): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.957+4699_957+4706d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315053 | AAGGGAGG others(13): Show |
A | 2 | a0002c0002t0002g0037 a0002c0002t0002g0055 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.957+4687_957+4706d others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315053 | |||||||
chr3:160315059 | G | GGGAGGGA others(8): Show |
1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+4686_957+4700d others(17): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315059 | |||||||
chr3:160315175 | T | C | 34 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0004 others(31): Show |
37 | HG01069.hp2 HG01243.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.957+4585A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315175 | |||||||
chr3:160315176 | G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+4584C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315176 | |||||||
chr3:160315177 | T | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+4583A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315177 | |||||||
chr3:160315296 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.957+4464C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315296 | |||||||
chr3:160315809 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+3951A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315809 | |||||||
chr3:160315810 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957+3950T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315810 | |||||||
chr3:160315847 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.957+3913C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315847 | |||||||
chr3:160315987 | G | T | 4 | a0002c0002t0003g0002 a0002c0002t0003g0030 a0002c0002t0003g0031 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+3773C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160315987 | |||||||
chr3:160316371 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.957+3389C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316371 | |||||||
chr3:160316767 | T | A | 2 | a0001c0001t0006g0198 a0001c0001t0006g0200 |
2 | NA18747.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+2993A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316767 | |||||||
chr3:160316786 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.957+2974T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316786 | |||||||
chr3:160316787 | A | G | 2 | a0001c0001t0006g0198 a0001c0001t0006g0200 |
2 | NA18747.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.957+2973T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316787 | |||||||
chr3:160316925 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+2835G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160316925 | |||||||
chr3:160317002 | A | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+2758T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317002 | |||||||
chr3:160317152 | A | G | 1 | a0002c0002t0002g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.957+2608T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317152 | |||||||
chr3:160317450 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.957+2310A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160317450 | |||||||
chr3:160318161 | T | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.957+1599A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318161 | |||||||
chr3:160318275 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.957+1485C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318275 | |||||||
chr3:160318288 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.957+1472A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318288 | |||||||
chr3:160318449 | G | A | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+1311C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318449 | |||||||
chr3:160318612 | A | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.957+1148T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318612 | |||||||
chr3:160318660 | G | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.957+1100C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318660 | |||||||
chr3:160318900 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.957+860G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160318900 | |||||||
chr3:160319555 | G | A | 9 | a0002c0002t0002g0037 a0002c0002t0003g0002 a0002c0002t0003g0029 others(6): Show |
10 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.957+205C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160319555 | |||||||
chr3:160319687 | A | G | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.957+73T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 9/19 | chr3 | 160319687 | |||||||
chr3:160320116 | G | A | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.778-177C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320116 | |||||||
chr3:160320184 | T | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(41): Show |
45 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.778-245A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320184 | |||||||
chr3:160320441 | T | TA | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-503dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320441 | |||||||
chr3:160320525 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.778-586A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160320525 | |||||||
chr3:160321340 | A | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-1401T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321340 | |||||||
chr3:160321363 | T | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-1424A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321363 | |||||||
chr3:160321388 | T | G | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-1449A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321388 | |||||||
chr3:160321676 | C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-1737G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321676 | |||||||
chr3:160321818 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.778-1879A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321818 | |||||||
chr3:160321999 | G | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0176 a0001c0001t0001g0182 others(2): Show |
5 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-2060C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160321999 | |||||||
chr3:160322003 | G | GTTAT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
15 | HG00280.hp2 HG02257.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.778-2068_778-2065d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | |||||||
chr3:160322003 | GTTAT | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
47 | HG00099.hp2 HG01243.hp1 HG01891.hp2 others(44): Show |
intron_variant | MODIFIER | c.778-2068_778-2065d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | |||||||
chr3:160322003 | GTTATTTA others(1): Show |
G | 38 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(35): Show |
39 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.778-2072_778-2065d others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322003 | |||||||
chr3:160322007 | T | C | 1 | a0002c0002t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.778-2068A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322007 | |||||||
chr3:160322011 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
23 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.778-2072A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322011 | |||||||
chr3:160322079 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.778-2140A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322079 | |||||||
chr3:160322091 | T | C | 1 | a0001c0001t0010g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.778-2152A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322091 | |||||||
chr3:160322194 | C | T | 14 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(11): Show |
14 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-2255G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322194 | |||||||
chr3:160322277 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.778-2338G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322277 | |||||||
chr3:160322763 | GA | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-2825delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322763 | |||||||
chr3:160322916 | A | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-2977T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160322916 | |||||||
chr3:160323002 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.778-3063A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323002 | |||||||
chr3:160323028 | C | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(29): Show |
33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.778-3089G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323028 | |||||||
chr3:160323152 | G | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778-3213C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323152 | |||||||
chr3:160323251 | A | G | 1 | a0002c0002t0004g0043 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.778-3312T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323251 | |||||||
chr3:160323290 | G | C | 2 | a0002c0003t0002g0050 a0002c0003t0002g0051 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.778-3351C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323290 | |||||||
chr3:160323318 | C | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3379G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323318 | |||||||
chr3:160323323 | G | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3384C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323323 | |||||||
chr3:160323351 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3412T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323351 | |||||||
chr3:160323354 | C | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3415G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323354 | |||||||
chr3:160323355 | G | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3416C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323355 | |||||||
chr3:160323356 | G | A | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3417C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323356 | |||||||
chr3:160323358 | A | AT | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3420dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323358 | |||||||
chr3:160323361 | A | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3422T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323361 | |||||||
chr3:160323371 | G | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3432C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323371 | |||||||
chr3:160323390 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3451T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323390 | |||||||
chr3:160323395 | A | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3456T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323395 | |||||||
chr3:160323434 | C | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3495G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323434 | |||||||
chr3:160323435 | T | C | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3496A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323435 | |||||||
chr3:160323617 | A | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-3678T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323617 | |||||||
chr3:160323695 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.778-3756G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160323695 | |||||||
chr3:160324307 | C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-4368G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324307 | |||||||
chr3:160324308 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-4369G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324308 | |||||||
chr3:160324409 | C | G | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.778-4470G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324409 | |||||||
chr3:160324431 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.778-4492T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324431 | |||||||
chr3:160324440 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.778-4501A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324440 | |||||||
chr3:160324525 | AAAC | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-4589_778-4587d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324525 | |||||||
chr3:160324556 | A | T | 2 | a0002c0002t0003g0030 a0002c0002t0003g0031 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.778-4617T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324556 | |||||||
chr3:160324671 | G | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-4732C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324671 | |||||||
chr3:160324713 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-4774G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324713 | |||||||
chr3:160324822 | A | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-4883T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324822 | |||||||
chr3:160324837 | A | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-4898T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324837 | |||||||
chr3:160324863 | C | T | 1 | a0002c0002t0003g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.778-4924G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324863 | |||||||
chr3:160324884 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-4945A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324884 | |||||||
chr3:160324893 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-4954G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324893 | |||||||
chr3:160324989 | G | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-5050C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324989 | |||||||
chr3:160324999 | G | C | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.778-5060C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160324999 | |||||||
chr3:160325003 | C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-5064G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325003 | |||||||
chr3:160325073 | G | T | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.778-5134C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325073 | |||||||
chr3:160325140 | G | C | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.778-5201C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325140 | |||||||
chr3:160325249 | A | G | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.778-5310T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325249 | |||||||
chr3:160325668 | A | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-5729T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325668 | |||||||
chr3:160325751 | T | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-5812A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325751 | |||||||
chr3:160325782 | T | C | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.778-5843A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160325782 | |||||||
chr3:160326044 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-6105A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326044 | |||||||
chr3:160326094 | T | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-6155A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326094 | |||||||
chr3:160326284 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-6345G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326284 | |||||||
chr3:160326432 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-6493A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326432 | |||||||
chr3:160326538 | G | A | 2 | a0002c0003t0002g0080 a0002c0003t0002g0081 |
2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.778-6599C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326538 | |||||||
chr3:160326903 | T | A | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.778-6964A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160326903 | |||||||
chr3:160327279 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.778-7340G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327279 | |||||||
chr3:160327438 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0134 a0001c0001t0001g0136 others(2): Show |
5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-7499G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327438 | |||||||
chr3:160327475 | C | G | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.778-7536G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327475 | |||||||
chr3:160327628 | G | C | 3 | a0002c0002t0002g0048 a0002c0002t0002g0049 a0002c0002t0002g0082 |
3 | HG01069.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.778-7689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327628 | |||||||
chr3:160327695 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-7756A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327695 | |||||||
chr3:160327747 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.778-7808G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327747 | |||||||
chr3:160327785 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.778-7846A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327785 | |||||||
chr3:160327981 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.778-8042G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160327981 | |||||||
chr3:160328155 | C | A | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-8216G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328155 | |||||||
chr3:160328389 | A | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.778-8450T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328389 | |||||||
chr3:160328461 | C | CA | 78 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.778-8523dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328461 | |||||||
chr3:160328697 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-8758C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328697 | |||||||
chr3:160328774 | G | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-8835C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328774 | |||||||
chr3:160328962 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.778-9023T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328962 | |||||||
chr3:160328991 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-9052A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328991 | |||||||
chr3:160328992 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.778-9053C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160328992 | |||||||
chr3:160329211 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778-9272A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329211 | |||||||
chr3:160329335 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-9396A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329335 | |||||||
chr3:160329462 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.778-9523G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329462 | |||||||
chr3:160329518 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.778-9579A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329518 | |||||||
chr3:160329620 | A | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-9681T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329620 | |||||||
chr3:160329652 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.778-9713A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329652 | |||||||
chr3:160329671 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0145 |
2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.778-9732G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329671 | |||||||
chr3:160329794 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-9855A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329794 | |||||||
chr3:160329824 | CT | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(31): Show |
35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.778-9886delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329824 | |||||||
chr3:160329932 | T | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-9993A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160329932 | |||||||
chr3:160330076 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-10137C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330076 | |||||||
chr3:160330197 | C | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0175 others(3): Show |
6 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-10258G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330197 | |||||||
chr3:160330377 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.778-10438G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330377 | |||||||
chr3:160330420 | A | G | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-10481T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330420 | |||||||
chr3:160330530 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.778-10591T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330530 | |||||||
chr3:160330687 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-10748A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330687 | |||||||
chr3:160330754 | C | T | 1 | a0002c0003t0002g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-10815G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330754 | |||||||
chr3:160330886 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-10947C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330886 | |||||||
chr3:160330928 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-10989C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160330928 | |||||||
chr3:160331111 | G | A | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.778-11172C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331111 | |||||||
chr3:160331113 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-11174G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331113 | |||||||
chr3:160331228 | G | A | 1 | a0002c0003t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.778-11289C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331228 | |||||||
chr3:160331265 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778-11326A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331265 | |||||||
chr3:160331379 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.778-11440A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331379 | |||||||
chr3:160331668 | A | AT | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.778-11730dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331668 | |||||||
chr3:160331720 | A | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-11781T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160331720 | |||||||
chr3:160332012 | TC | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-12074delG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332012 | |||||||
chr3:160332039 | T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-12100A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332039 | |||||||
chr3:160332040 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-12101G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332040 | |||||||
chr3:160332045 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-12106C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332045 | |||||||
chr3:160332389 | G | T | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-12450C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332389 | |||||||
chr3:160332878 | G | A | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-12939C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332878 | |||||||
chr3:160332925 | A | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.778-12986T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160332925 | |||||||
chr3:160333036 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.778-13097T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333036 | |||||||
chr3:160333046 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-13107A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333046 | |||||||
chr3:160333076 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.778-13137G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333076 | |||||||
chr3:160333189 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-13250G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333189 | |||||||
chr3:160333264 | T | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0134 a0001c0001t0001g0136 others(2): Show |
5 | HG00323.hp1 HG01358.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-13325A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333264 | |||||||
chr3:160333345 | A | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-13406T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333345 | |||||||
chr3:160333434 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.778-13495A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333434 | |||||||
chr3:160333732 | A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-13793T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333732 | |||||||
chr3:160333923 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.778-13984G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333923 | |||||||
chr3:160333988 | G | A | 2 | a0002c0002t0004g0018 a0002c0002t0004g0020 |
2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.778-14049C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160333988 | |||||||
chr3:160334062 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(2): Show |
5 | HG00099.hp2 HG03834.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-14123C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334062 | |||||||
chr3:160334428 | C | CT | 75 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.778-14490dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334428 | |||||||
chr3:160334593 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.778-14654A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334593 | |||||||
chr3:160334606 | G | A | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.778-14667C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334606 | |||||||
chr3:160334647 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.778-14708G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334647 | |||||||
chr3:160334690 | C | G | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.778-14751G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334690 | |||||||
chr3:160334805 | CT | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.778-14867delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334805 | |||||||
chr3:160334828 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-14889A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160334828 | |||||||
chr3:160335021 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-15082A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335021 | |||||||
chr3:160335034 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.778-15095G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335034 | |||||||
chr3:160335097 | C | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-15158G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335097 | |||||||
chr3:160335131 | T | C | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-15192A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335131 | |||||||
chr3:160335142 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-15203T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335142 | |||||||
chr3:160335147 | C | CT | 5 | a0002c0002t0001g0033 a0002c0002t0001g0063 a0002c0002t0002g0003 others(2): Show |
6 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-15209dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335147 | |||||||
chr3:160335449 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-15510A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335449 | |||||||
chr3:160335672 | G | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.778-15733C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335672 | |||||||
chr3:160335744 | C | T | 37 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.778-15805G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335744 | |||||||
chr3:160335926 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.778-15987C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335926 | |||||||
chr3:160335980 | A | G | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.778-16041T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160335980 | |||||||
chr3:160336156 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-16217A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336156 | |||||||
chr3:160336459 | GAA | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-16522_778-1652 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336459 | |||||||
chr3:160336501 | T | A | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.778-16562A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336501 | |||||||
chr3:160336591 | A | ATGTG | 9 | a0001c0001t0001g0199 a0002c0002t0002g0021 a0002c0002t0002g0022 others(6): Show |
9 | HG01070.hp2 HG01255.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-16656_778-1665 others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336591 | |||||||
chr3:160336764 | T | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-16825A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160336764 | |||||||
chr3:160337061 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.778-17122A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337061 | |||||||
chr3:160337156 | TTA | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.778-17219_778-1721 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337156 | |||||||
chr3:160337176 | A | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.778-17237T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337176 | |||||||
chr3:160337363 | C | T | 6 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-17424G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337363 | |||||||
chr3:160337759 | T | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778-17820A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337759 | |||||||
chr3:160337770 | C | T | 4 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0204 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-17831G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160337770 | |||||||
chr3:160338091 | A | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+17922T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338091 | |||||||
chr3:160338631 | C | CA | 9 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 others(6): Show |
9 | HG01069.hp2 HG01891.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+17381dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338631 | |||||||
chr3:160338645 | A | G | 2 | a0002c0002t0003g0030 a0002c0002t0003g0031 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.777+17368T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338645 | |||||||
chr3:160338743 | C | A | 1 | a0002c0002t0002g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.777+17270G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338743 | |||||||
chr3:160338855 | G | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.777+17158C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338855 | |||||||
chr3:160338935 | A | G | 2 | a0002c0002t0004g0018 a0002c0002t0004g0020 |
2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.777+17078T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160338935 | |||||||
chr3:160339325 | T | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+16688A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339325 | |||||||
chr3:160339427 | T | A | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.777+16586A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339427 | |||||||
chr3:160339531 | C | T | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+16482G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339531 | |||||||
chr3:160339931 | G | A | 3 | a0002c0002t0001g0056 a0002c0002t0001g0070 a0002c0002t0001g0071 |
3 | HG00735.hp1 HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.777+16082C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160339931 | |||||||
chr3:160340181 | G | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+15832C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340181 | |||||||
chr3:160340272 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.777+15741A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340272 | |||||||
chr3:160340338 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.777+15675T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340338 | |||||||
chr3:160340394 | C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+15619G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340394 | |||||||
chr3:160340484 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+15529C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340484 | |||||||
chr3:160340774 | G | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.777+15239C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340774 | |||||||
chr3:160340815 | C | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777+15198G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160340815 | |||||||
chr3:160341016 | C | CT | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+14996dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341016 | |||||||
chr3:160341342 | TTA | T | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+14669_777+1467 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341342 | |||||||
chr3:160341343 | TA | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
35 | HG00099.hp2 HG01255.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+14669delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341343 | |||||||
chr3:160341343 | TAA | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.777+14668_777+1466 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341343 | |||||||
chr3:160341600 | C | T | 1 | a0002c0002t0003g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.777+14413G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341600 | |||||||
chr3:160341660 | A | G | 1 | a0005c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.777+14353T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341660 | |||||||
chr3:160341849 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+14164C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341849 | |||||||
chr3:160341979 | A | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+14034T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160341979 | |||||||
chr3:160342003 | G | A | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+14010C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342003 | |||||||
chr3:160342102 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+13911A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342102 | |||||||
chr3:160342785 | T | G | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+13228A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342785 | |||||||
chr3:160342810 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+13203A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342810 | |||||||
chr3:160342960 | C | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.777+13053G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342960 | |||||||
chr3:160342986 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+13027A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160342986 | |||||||
chr3:160343150 | C | T | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+12863G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343150 | |||||||
chr3:160343357 | G | A | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+12656C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343357 | |||||||
chr3:160343730 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+12283C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343730 | |||||||
chr3:160343754 | C | T | 1 | a0002c0002t0002g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+12259G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343754 | |||||||
chr3:160343768 | A | C | 4 | a0002c0002t0002g0157 a0002c0002t0002g0158 a0002c0002t0002g0159 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+12245T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160343768 | |||||||
chr3:160344039 | G | A | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.777+11974C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344039 | |||||||
chr3:160344075 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.777+11938T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344075 | |||||||
chr3:160344106 | G | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11907C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344106 | |||||||
chr3:160344162 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+11851G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344162 | |||||||
chr3:160344245 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+11768C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344245 | |||||||
chr3:160344527 | C | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11486G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344527 | |||||||
chr3:160344618 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+11395C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344618 | |||||||
chr3:160344874 | A | G | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777+11139T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160344874 | |||||||
chr3:160345193 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+10820A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345193 | |||||||
chr3:160345277 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.777+10736A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345277 | |||||||
chr3:160345400 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+10613A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345400 | |||||||
chr3:160345450 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0178 |
3 | HG00642.hp2 HG01891.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.777+10563C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345450 | |||||||
chr3:160345525 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.777+10488A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345525 | |||||||
chr3:160345526 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.777+10487T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345526 | |||||||
chr3:160345568 | A | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.777+10445T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345568 | |||||||
chr3:160345587 | G | A | 3 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0205 |
3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+10426C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345587 | |||||||
chr3:160345693 | C | CA | 75 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0101 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.777+10319dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | |||||||
chr3:160345693 | C | CAA | 8 | a0001c0001t0001g0176 a0001c0001t0001g0196 a0001c0001t0001g0199 others(5): Show |
8 | HG01070.hp2 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+10318_777+1031 others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | |||||||
chr3:160345693 | CA | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG00099.hp2 HG01255.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.777+10319delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345693 | |||||||
chr3:160345822 | T | A | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+10191A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345822 | |||||||
chr3:160345961 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+10052A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160345961 | |||||||
chr3:160346705 | G | T | 10 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0116 others(7): Show |
10 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.777+9308C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346705 | |||||||
chr3:160346731 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+9282C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346731 | |||||||
chr3:160346999 | G | A | 3 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0205 |
3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+9014C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160346999 | |||||||
chr3:160347111 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.777+8902G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347111 | |||||||
chr3:160347122 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+8891G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347122 | |||||||
chr3:160347334 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.777+8679A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347334 | |||||||
chr3:160347429 | T | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02258.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+8584A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347429 | |||||||
chr3:160347629 | C | G | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+8384G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347629 | |||||||
chr3:160347698 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0147 |
2 | HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.777+8315T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347698 | |||||||
chr3:160347780 | C | T | 151 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.777+8233G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347780 | |||||||
chr3:160347968 | A | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+8045T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347968 | |||||||
chr3:160347975 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+8038G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347975 | |||||||
chr3:160347978 | T | G | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+8035A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160347978 | |||||||
chr3:160348074 | A | G | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0119 others(5): Show |
8 | HG00323.hp1 HG01358.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+7939T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348074 | |||||||
chr3:160348198 | T | C | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+7815A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348198 | |||||||
chr3:160348234 | A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+7779T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348234 | |||||||
chr3:160348240 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+7773A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160348240 | |||||||
chr3:160349010 | C | T | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+7003G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349010 | |||||||
chr3:160349070 | T | C | 4 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0204 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6943A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349070 | |||||||
chr3:160349108 | A | AT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(41): Show |
45 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.777+6904dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349108 | |||||||
chr3:160349586 | T | A | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+6427A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349586 | |||||||
chr3:160349931 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.777+6082A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160349931 | |||||||
chr3:160350142 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+5871A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350142 | |||||||
chr3:160350243 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0147 |
3 | HG00323.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.777+5770G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350243 | |||||||
chr3:160350304 | T | C | 1 | a0002c0002t0002g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+5709A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350304 | |||||||
chr3:160350340 | C | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02258.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+5673G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350340 | |||||||
chr3:160350371 | T | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+5642A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350371 | |||||||
chr3:160350415 | CA | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.777+5597delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350415 | |||||||
chr3:160350415 | CAA | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(37): Show |
41 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.777+5596_777+5597d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350415 | |||||||
chr3:160350690 | G | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+5323C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160350690 | |||||||
chr3:160351017 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.777+4996A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351017 | |||||||
chr3:160351575 | ATATAT | A | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.777+4433_777+4437d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351575 | |||||||
chr3:160351628 | T | C | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.777+4385A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351628 | |||||||
chr3:160351693 | CATAAAAA others(40): Show |
C | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+4273_777+4319d others(49): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351693 | |||||||
chr3:160351740 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.777+4273A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160351740 | |||||||
chr3:160352017 | AT | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.777+3995delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352017 | |||||||
chr3:160352276 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.777+3737C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352276 | |||||||
chr3:160352290 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.777+3723C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352290 | |||||||
chr3:160352725 | G | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+3288C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352725 | |||||||
chr3:160352994 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+3019G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160352994 | |||||||
chr3:160353119 | A | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.777+2894T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353119 | |||||||
chr3:160353184 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.777+2829A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353184 | |||||||
chr3:160353233 | A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.777+2780T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353233 | |||||||
chr3:160353240 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+2773T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353240 | |||||||
chr3:160353489 | A | G | 4 | a0002c0002t0002g0157 a0002c0002t0002g0158 a0002c0002t0002g0159 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+2524T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353489 | |||||||
chr3:160353505 | A | G | 1 | a0002c0002t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.777+2508T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353505 | |||||||
chr3:160353520 | T | C | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+2493A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353520 | |||||||
chr3:160353598 | C | T | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+2415G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353598 | |||||||
chr3:160353630 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.777+2383G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160353630 | |||||||
chr3:160354232 | T | G | 24 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.777+1781A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354232 | |||||||
chr3:160354273 | A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.777+1740T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354273 | |||||||
chr3:160354477 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.777+1536C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354477 | |||||||
chr3:160354590 | C | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.777+1423G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354590 | |||||||
chr3:160354661 | AT | A | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1351delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160354661 | |||||||
chr3:160355090 | G | A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+923C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355090 | |||||||
chr3:160355249 | G | GTTAT | 3 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0178 |
3 | HG00642.hp2 HG01891.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.777+760_777+763dup others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355249 | |||||||
chr3:160355480 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.777+533C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355480 | |||||||
chr3:160355603 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.777+410G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355603 | |||||||
chr3:160355743 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+270T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355743 | |||||||
chr3:160355993 | T | C | 1 | a0002c0002t0001g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.777+20A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 8/19 | chr3 | 160355993 | |||||||
chr3:160356208 | A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.640-58T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356208 | |||||||
chr3:160356417 | T | C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.640-267A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356417 | |||||||
chr3:160356512 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.640-362A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356512 | |||||||
chr3:160356796 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.640-646A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356796 | |||||||
chr3:160356979 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.639+510T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160356979 | |||||||
chr3:160357259 | C | A | 1 | a0002c0003t0002g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.639+230G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 7/19 | chr3 | 160357259 | |||||||
chr3:160357768 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.550-190G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357768 | |||||||
chr3:160357868 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.550-290C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357868 | |||||||
chr3:160357995 | CTTAT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-421_550-418del others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160357995 | |||||||
chr3:160358156 | T | C | 20 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(17): Show |
21 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.550-578A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358156 | |||||||
chr3:160358248 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.550-670T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358248 | |||||||
chr3:160358292 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-714G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358292 | |||||||
chr3:160358293 | G | A | 4 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-715C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160358293 | |||||||
chr3:160359208 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.550-1630G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359208 | |||||||
chr3:160359257 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-1679C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359257 | |||||||
chr3:160359410 | G | A | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.550-1832C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359410 | |||||||
chr3:160359550 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.550-1972G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359550 | |||||||
chr3:160359558 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.550-1980G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359558 | |||||||
chr3:160359856 | A | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.550-2278T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160359856 | |||||||
chr3:160360018 | A | G | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-2440T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360018 | |||||||
chr3:160360058 | A | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.550-2480T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360058 | |||||||
chr3:160360145 | G | A | 1 | a0004c0007t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.550-2567C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360145 | |||||||
chr3:160360155 | C | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.550-2577G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360155 | |||||||
chr3:160360353 | A | G | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-2775T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360353 | |||||||
chr3:160360954 | A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-3376T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360954 | |||||||
chr3:160360991 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.550-3413C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160360991 | |||||||
chr3:160361002 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.550-3424C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361002 | |||||||
chr3:160361086 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.550-3508A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361086 | |||||||
chr3:160361443 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.550-3865A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361443 | |||||||
chr3:160361498 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.550-3920G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361498 | |||||||
chr3:160361613 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.550-4035G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361613 | |||||||
chr3:160361617 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.550-4039A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361617 | |||||||
chr3:160361740 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.550-4162G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361740 | |||||||
chr3:160361759 | C | T | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.550-4181G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160361759 | |||||||
chr3:160363016 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+3027G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363016 | |||||||
chr3:160363031 | G | C | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+3012C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363031 | |||||||
chr3:160363123 | T | C | 1 | a0002c0002t0003g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.549+2920A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363123 | |||||||
chr3:160363192 | G | A | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.549+2851C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363192 | |||||||
chr3:160363401 | G | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.549+2642C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363401 | |||||||
chr3:160363866 | G | T | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.549+2177C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363866 | |||||||
chr3:160363911 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.549+2132C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160363911 | |||||||
chr3:160364071 | C | T | 1 | a0003c0004t0002g0027 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.549+1972G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364071 | |||||||
chr3:160364283 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.549+1760A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364283 | |||||||
chr3:160364293 | C | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.549+1750G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364293 | |||||||
chr3:160364366 | A | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.549+1677T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364366 | |||||||
chr3:160364496 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.549+1547A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364496 | |||||||
chr3:160364589 | C | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG01981.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.549+1454G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364589 | |||||||
chr3:160364885 | G | A | 2 | a0002c0002t0002g0004 a0002c0002t0002g0028 |
3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.549+1158C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160364885 | |||||||
chr3:160365002 | T | TA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(35): Show |
39 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.549+1040dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365002 | |||||||
chr3:160365013 | GA | G | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.549+1029delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365013 | |||||||
chr3:160365712 | G | T | 2 | a0002c0002t0002g0048 a0002c0002t0002g0082 |
2 | HG01069.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.549+331C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365712 | |||||||
chr3:160365793 | C | T | 2 | a0001c0001t0001g0115 a0002c0002t0002g0015 |
2 | HG00741.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.549+250G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365793 | |||||||
chr3:160365997 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+46G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160365997 | |||||||
chr3:160366027 | A | G | 1 | a0001c0001t0010g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.549+16T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 6/19 | chr3 | 160366027 | |||||||
chr3:160366278 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.440-126A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160366278 | |||||||
chr3:160366786 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.440-634A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160366786 | |||||||
chr3:160367084 | T | C | 3 | a0002c0002t0002g0202 a0002c0002t0002g0203 a0002c0002t0002g0205 |
3 | HG02965.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.440-932A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367084 | |||||||
chr3:160367112 | AT | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-961delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367112 | |||||||
chr3:160367500 | C | T | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-1348G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367500 | |||||||
chr3:160367613 | A | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-1461T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367613 | |||||||
chr3:160367860 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440-1708A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367860 | |||||||
chr3:160367878 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440-1726G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160367878 | |||||||
chr3:160368215 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.440-2063C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368215 | |||||||
chr3:160368267 | G | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.440-2115C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368267 | |||||||
chr3:160368359 | C | CA | 10 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0139 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-2208dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | |||||||
chr3:160368359 | CA | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.440-2208delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | |||||||
chr3:160368359 | CAA | C | 8 | a0001c0001t0001g0197 a0002c0002t0001g0068 a0002c0002t0002g0156 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-2209_440-2208d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368359 | |||||||
chr3:160368518 | T | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-2366A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368518 | |||||||
chr3:160368649 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.440-2497C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368649 | |||||||
chr3:160368713 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
25 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.440-2561G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368713 | |||||||
chr3:160368796 | A | AAT | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.440-2646_440-2645d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368796 | |||||||
chr3:160368875 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.440-2723C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368875 | |||||||
chr3:160368930 | T | TA | 2 | a0002c0002t0001g0084 a0002c0002t0001g0085 |
2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.440-2779dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160368930 | |||||||
chr3:160369005 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.440-2853G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369005 | |||||||
chr3:160369262 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.440-3110T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369262 | |||||||
chr3:160369463 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.440-3311G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369463 | |||||||
chr3:160369832 | T | G | 1 | a0002c0002t0003g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.440-3680A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369832 | |||||||
chr3:160369965 | G | A | 1 | a0002c0002t0004g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.440-3813C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160369965 | |||||||
chr3:160370144 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.440-3992G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370144 | |||||||
chr3:160370243 | A | C | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02258.hp1 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-4091T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370243 | |||||||
chr3:160370359 | T | C | 1 | a0002c0003t0002g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.440-4207A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370359 | |||||||
chr3:160370375 | A | AT | 28 | a0001c0001t0001g0112 a0001c0001t0001g0168 a0001c0001t0001g0169 others(25): Show |
28 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.440-4224dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370375 | |||||||
chr3:160370375 | A | ATT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0171 a0001c0001t0001g0189 others(8): Show |
12 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.440-4225_440-4224d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370375 | |||||||
chr3:160370420 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440-4268G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370420 | |||||||
chr3:160370561 | A | AT | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-4410dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370561 | |||||||
chr3:160370651 | C | T | 4 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0034 others(1): Show |
5 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-4499G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370651 | |||||||
chr3:160370965 | A | G | 3 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0081 |
3 | HG00738.hp2 HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.440-4813T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160370965 | |||||||
chr3:160371013 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.439+4799A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371013 | |||||||
chr3:160371248 | A | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+4564T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371248 | |||||||
chr3:160371253 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.439+4559G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371253 | |||||||
chr3:160371363 | C | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0176 others(4): Show |
7 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+4449G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371363 | |||||||
chr3:160371633 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+4179C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371633 | |||||||
chr3:160371660 | C | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+4152G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371660 | |||||||
chr3:160371944 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.439+3868A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160371944 | |||||||
chr3:160372029 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.439+3783G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372029 | |||||||
chr3:160372108 | G | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+3704C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372108 | |||||||
chr3:160372206 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439+3606G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372206 | |||||||
chr3:160372246 | T | C | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.439+3566A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372246 | |||||||
chr3:160372290 | G | C | 1 | a0001c0001t0006g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.439+3522C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372290 | |||||||
chr3:160372702 | T | C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+3110A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160372702 | |||||||
chr3:160373189 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+2623A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373189 | |||||||
chr3:160373197 | G | A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+2615C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373197 | |||||||
chr3:160373578 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.439+2234T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373578 | |||||||
chr3:160373772 | A | T | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.439+2040T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373772 | |||||||
chr3:160373913 | C | T | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+1899G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373913 | |||||||
chr3:160373920 | C | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.439+1892G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160373920 | |||||||
chr3:160374323 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.439+1489G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374323 | |||||||
chr3:160374366 | G | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.439+1446C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374366 | |||||||
chr3:160374713 | T | C | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+1099A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374713 | |||||||
chr3:160374781 | C | T | 2 | a0003c0004t0002g0026 a0003c0004t0002g0027 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.439+1031G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374781 | |||||||
chr3:160374838 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.439+974C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160374838 | |||||||
chr3:160375010 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.439+802G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375010 | |||||||
chr3:160375497 | T | A | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.439+315A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375497 | |||||||
chr3:160375647 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.439+165T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375647 | |||||||
chr3:160375726 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.439+86C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 5/19 | chr3 | 160375726 | |||||||
chr3:160375890 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.371-10C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160375890 | |||||||
chr3:160375973 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.371-93C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160375973 | |||||||
chr3:160376104 | C | T | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.371-224G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376104 | |||||||
chr3:160376247 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.371-367T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376247 | |||||||
chr3:160376356 | AG | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-477delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160376356 | |||||||
chr3:160377199 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.370+231C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377199 | |||||||
chr3:160377232 | G | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.370+198C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377232 | |||||||
chr3:160377351 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370+79G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377351 | |||||||
chr3:160377356 | T | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.370+74A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 4/19 | chr3 | 160377356 | |||||||
chr3:160377658 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.260-118G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160377658 | |||||||
chr3:160378240 | T | TA | 11 | a0002c0002t0002g0037 a0002c0002t0002g0055 a0002c0002t0002g0202 others(8): Show |
12 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-701dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378240 | |||||||
chr3:160378567 | A | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.260-1027T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378567 | |||||||
chr3:160378646 | T | A | 6 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-1106A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378646 | |||||||
chr3:160378833 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260-1293C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378833 | |||||||
chr3:160378847 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.260-1307T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378847 | |||||||
chr3:160378854 | A | G | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1314T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160378854 | |||||||
chr3:160379318 | T | C | 1 | a0002c0002t0002g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.260-1778A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379318 | |||||||
chr3:160379560 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+1943C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379560 | |||||||
chr3:160379691 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.259+1812A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160379691 | |||||||
chr3:160380007 | G | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+1496C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380007 | |||||||
chr3:160380036 | CT | C | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+1466delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380036 | |||||||
chr3:160380094 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259+1409C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380094 | |||||||
chr3:160380125 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.259+1378G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380125 | |||||||
chr3:160380128 | G | A | 6 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0062 others(3): Show |
6 | HG00423.hp2 HG00558.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+1375C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380128 | |||||||
chr3:160380200 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.259+1303T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380200 | |||||||
chr3:160380241 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259+1262A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380241 | |||||||
chr3:160380537 | C | T | 5 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(2): Show |
5 | NA18960.hp1 NA18983.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+966G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380537 | |||||||
chr3:160380549 | G | A | 2 | a0002c0002t0002g0032 a0002c0002t0002g0036 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.259+954C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380549 | |||||||
chr3:160380705 | GT | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.259+797delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380705 | |||||||
chr3:160380707 | G | GA | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(25): Show |
29 | HG00099.hp2 HG01069.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.259+795dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380707 | |||||||
chr3:160380708 | A | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.259+795T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380708 | |||||||
chr3:160380749 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.259+754G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380749 | |||||||
chr3:160380902 | A | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+601T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380902 | |||||||
chr3:160380927 | C | G | 1 | a0002c0003t0008g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259+576G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380927 | |||||||
chr3:160380975 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.259+528G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160380975 | |||||||
chr3:160381010 | A | G | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+493T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381010 | |||||||
chr3:160381071 | C | CA | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+431dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381071 | |||||||
chr3:160381080 | T | G | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+423A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381080 | |||||||
chr3:160381227 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.259+276T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381227 | |||||||
chr3:160381231 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.259+272G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381231 | |||||||
chr3:160381239 | A | AAT | 21 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0100 others(18): Show |
23 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.259+262_259+263dup others(2): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATAT | 17 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(14): Show |
18 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+260_259+263dup others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(1): Show |
9 | a0002c0002t0002g0048 a0002c0002t0004g0018 a0002c0002t0004g0019 others(6): Show |
9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+256_259+263dup others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(3): Show |
4 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0065 others(1): Show |
4 | HG02257.hp1 HG03579.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+254_259+263dup others(10): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(5): Show |
12 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0176 others(9): Show |
12 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+252_259+263dup others(12): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(7): Show |
6 | a0001c0001t0001g0181 a0001c0001t0001g0199 a0002c0002t0001g0062 others(3): Show |
6 | HG00423.hp2 HG01070.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+250_259+263dup others(14): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(9): Show |
8 | a0001c0001t0001g0180 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG00323.hp2 HG00423.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+248_259+263dup others(16): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(11): Show |
6 | a0001c0001t0001g0171 a0001c0001t0001g0193 a0001c0001t0001g0194 others(3): Show |
6 | HG01433.hp2 HG01891.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+246_259+263dup others(18): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(13): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0175 others(4): Show |
8 | HG00642.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+244_259+263dup others(20): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(15): Show |
6 | a0001c0001t0001g0169 a0001c0001t0001g0191 a0002c0002t0002g0204 others(3): Show |
6 | HG00738.hp1 HG02258.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+242_259+263dup others(22): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(17): Show |
4 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0002c0002t0001g0061 others(1): Show |
4 | HG01361.hp2 HG02293.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+240_259+263dup others(24): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(19): Show |
6 | a0001c0001t0001g0011 a0002c0002t0001g0076 a0002c0002t0002g0157 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+238_259+263dup others(26): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(21): Show |
5 | a0001c0001t0001g0009 a0002c0002t0001g0060 a0002c0002t0001g0070 others(2): Show |
5 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(28): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(23): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0177 a0002c0002t0001g0056 others(2): Show |
5 | HG00280.hp1 HG01358.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(30): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(25): Show |
3 | a0001c0001t0001g0008 a0002c0002t0001g0084 a0002c0002t0001g0085 |
3 | HG02602.hp1 HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.259+263_259+264ins others(32): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(27): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0002c0002t0001g0057 others(1): Show |
4 | HG00099.hp1 HG00558.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+263_259+264ins others(34): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(31): Show |
3 | a0002c0002t0001g0068 a0002c0002t0001g0069 a0002c0002t0001g0075 |
3 | HG00140.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.259+263_259+264ins others(38): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(33): Show |
2 | a0001c0001t0001g0007 a0002c0002t0001g0074 |
2 | HG01516.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.259+263_259+264ins others(40): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(35): Show |
1 | a0002c0002t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.259+263_259+264ins others(42): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | AATATATA others(39): Show |
1 | a0002c0002t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+263_259+264ins others(46): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | ATATATAT others(10): Show |
1 | a0002c0003t0002g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.259+263_259+264ins others(17): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381239 | A | ATATATAT others(24): Show |
1 | a0002c0002t0002g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259+263_259+264ins others(31): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381239 | |||||||
chr3:160381252 | A | T | 3 | a0002c0002t0001g0047 a0002c0002t0001g0066 a0002c0002t0001g0067 |
3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.259+251T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381252 | |||||||
chr3:160381253 | T | TA | 3 | a0002c0002t0001g0047 a0002c0002t0001g0066 a0002c0002t0001g0067 |
3 | HG03710.hp1 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.259+249dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381253 | |||||||
chr3:160381266 | T | A | 6 | a0002c0002t0001g0056 a0002c0002t0001g0068 a0002c0002t0001g0069 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+237A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381266 | |||||||
chr3:160381364 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259+139A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381364 | |||||||
chr3:160381388 | G | T | 1 | a0001c0001t0005g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+115C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381388 | |||||||
chr3:160381398 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+105A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381398 | |||||||
chr3:160381402 | G | A | 1 | a0001c0008t0001g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.259+101C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 3/19 | chr3 | 160381402 | |||||||
chr3:160381773 | A | G | 1 | a0002c0002t0002g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.38-49T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381773 | |||||||
chr3:160381867 | A | AT | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.38-144dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381867 | |||||||
chr3:160381967 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.38-243G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381967 | |||||||
chr3:160381973 | A | T | 6 | a0002c0002t0004g0018 a0002c0002t0004g0019 a0002c0002t0004g0020 others(3): Show |
6 | HG02976.hp2 NA18960.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-249T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160381973 | |||||||
chr3:160382899 | C | A | 1 | a0002c0002t0003g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.38-1175G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160382899 | |||||||
chr3:160383161 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+1403T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383161 | |||||||
chr3:160383538 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.37+1026C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383538 | |||||||
chr3:160383601 | A | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+963T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383601 | |||||||
chr3:160383857 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.37+707A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160383857 | |||||||
chr3:160384018 | G | C | 1 | a0002c0002t0002g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.37+546C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384018 | |||||||
chr3:160384218 | C | G | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.37+346G>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384218 | |||||||
chr3:160384245 | C | CA | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.37+318dupT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384245 | |||||||
chr3:160384245 | CA | C | 9 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(6): Show |
9 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+318delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384245 | |||||||
chr3:160384346 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+218C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384346 | |||||||
chr3:160384373 | A | G | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.37+191T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384373 | |||||||
chr3:160384381 | C | T | 6 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.37+183G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 2/19 | chr3 | 160384381 | |||||||
chr3:160384699 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-46-53G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384699 | |||||||
chr3:160384703 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-57A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384703 | |||||||
chr3:160384859 | A | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0094 a0001c0001t0001g0095 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-213T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160384859 | |||||||
chr3:160385012 | C | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0171 a0001c0001t0001g0189 others(10): Show |
14 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46-366G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385012 | |||||||
chr3:160385023 | T | C | 1 | a0002c0002t0004g0020 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-46-377A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385023 | |||||||
chr3:160385138 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0151 |
2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-46-492G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385138 | |||||||
chr3:160385149 | G | A | 2 | a0002c0002t0002g0004 a0002c0002t0002g0028 |
3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-46-503C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385149 | |||||||
chr3:160385187 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-46-541C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385187 | |||||||
chr3:160385282 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-636T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385282 | |||||||
chr3:160385335 | G | C | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-689C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385335 | |||||||
chr3:160385376 | A | G | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-730T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385376 | |||||||
chr3:160385431 | G | C | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-785C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385431 | |||||||
chr3:160385831 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-1185A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160385831 | |||||||
chr3:160386236 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-1590A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386236 | |||||||
chr3:160386569 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-46-1923A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386569 | |||||||
chr3:160386583 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-1937C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386583 | |||||||
chr3:160386711 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-46-2065G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386711 | |||||||
chr3:160386975 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-2329A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160386975 | |||||||
chr3:160387281 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-46-2635C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387281 | |||||||
chr3:160387453 | G | C | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-2807C>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387453 | |||||||
chr3:160387461 | G | A | 2 | a0003c0004t0002g0026 a0003c0004t0002g0027 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-46-2815C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387461 | |||||||
chr3:160387970 | T | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-3324A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160387970 | |||||||
chr3:160388021 | G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-3375C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388021 | |||||||
chr3:160388036 | AG | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-3391delC | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388036 | |||||||
chr3:160388216 | CT | C | 8 | a0001c0001t0001g0147 a0002c0002t0002g0004 a0002c0002t0002g0028 others(5): Show |
9 | HG00323.hp1 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-3571delA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388216 | |||||||
chr3:160388342 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-46-3696G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388342 | |||||||
chr3:160388493 | C | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-3847G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388493 | |||||||
chr3:160388541 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-46-3895G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388541 | |||||||
chr3:160388551 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-3905A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388551 | |||||||
chr3:160388565 | A | T | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-3919T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388565 | |||||||
chr3:160388654 | T | G | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-4008A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388654 | |||||||
chr3:160388764 | C | T | 1 | a0002c0002t0003g0002 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-46-4118G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388764 | |||||||
chr3:160388903 | G | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-4257C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388903 | |||||||
chr3:160388993 | C | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-46-4347G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160388993 | |||||||
chr3:160389042 | A | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-4396T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389042 | |||||||
chr3:160389312 | C | T | 28 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-4666G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389312 | |||||||
chr3:160389424 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-4778G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389424 | |||||||
chr3:160389502 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-4856G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389502 | |||||||
chr3:160389665 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-46-5019T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389665 | |||||||
chr3:160389691 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-5045G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389691 | |||||||
chr3:160389704 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-46-5058G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160389704 | |||||||
chr3:160390020 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-5374C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390020 | |||||||
chr3:160390050 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-5404A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390050 | |||||||
chr3:160390193 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-5547C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390193 | |||||||
chr3:160390272 | C | T | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-5626G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390272 | |||||||
chr3:160390372 | G | A | 1 | a0005c0005t0009g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-46-5726C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390372 | |||||||
chr3:160390417 | C | CAAAAAA | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-5777_-46-5772d others(8): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390417 | |||||||
chr3:160390536 | T | C | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-5890A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390536 | |||||||
chr3:160390591 | T | C | 3 | a0002c0002t0001g0076 a0002c0002t0001g0077 a0002c0002t0001g0078 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-5945A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390591 | |||||||
chr3:160390798 | T | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0028 a0002c0002t0002g0048 others(2): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-6152A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160390798 | |||||||
chr3:160391055 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-46-6409C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391055 | |||||||
chr3:160391252 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-46-6606G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391252 | |||||||
chr3:160391300 | A | G | 2 | a0002c0002t0003g0030 a0002c0002t0003g0031 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-46-6654T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391300 | |||||||
chr3:160391561 | C | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-6915G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391561 | |||||||
chr3:160391600 | G | A | 1 | a0001c0001t0006g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-46-6954C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391600 | |||||||
chr3:160391688 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-46-7042T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391688 | |||||||
chr3:160391809 | T | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46-7163A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391809 | |||||||
chr3:160391860 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(40): Show |
46 | HG00099.hp2 HG01069.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.-46-7214G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391860 | |||||||
chr3:160391869 | A | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-46-7223T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391869 | |||||||
chr3:160391944 | C | T | 1 | a0002c0002t0007g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+7202G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391944 | |||||||
chr3:160391969 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-47+7177C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160391969 | |||||||
chr3:160392424 | G | A | 9 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(6): Show |
9 | HG00738.hp2 HG01167.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+6722C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392424 | |||||||
chr3:160392467 | G | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(31): Show |
35 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+6679C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392467 | |||||||
chr3:160392745 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-47+6401A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392745 | |||||||
chr3:160392894 | A | AC | 19 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(16): Show |
20 | HG01069.hp2 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-47+6251dupG | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160392894 | |||||||
chr3:160393133 | C | A | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+6013G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393133 | |||||||
chr3:160393348 | G | A | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+5798C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393348 | |||||||
chr3:160393623 | G | A | 3 | a0002c0002t0001g0073 a0002c0002t0001g0074 a0002c0002t0001g0075 |
3 | HG00140.hp1 HG01106.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-47+5523C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393623 | |||||||
chr3:160393656 | T | C | 8 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(5): Show |
8 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+5490A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393656 | |||||||
chr3:160393671 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-47+5475A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160393671 | |||||||
chr3:160394069 | T | G | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+5077A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394069 | |||||||
chr3:160394101 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0021 a0002c0002t0002g0022 others(18): Show |
22 | HG01069.hp2 HG01255.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+5045G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394101 | |||||||
chr3:160394104 | T | C | 2 | a0002c0002t0002g0004 a0002c0002t0002g0028 |
3 | HG02886.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-47+5042A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394104 | |||||||
chr3:160394172 | A | T | 25 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.-47+4974T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394172 | |||||||
chr3:160394278 | T | A | 3 | a0002c0002t0002g0048 a0002c0002t0002g0049 a0002c0002t0002g0082 |
3 | HG01069.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-47+4868A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394278 | |||||||
chr3:160394546 | T | A | 5 | a0002c0003t0002g0050 a0002c0003t0002g0051 a0002c0003t0002g0052 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+4600A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394546 | |||||||
chr3:160394642 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-47+4504C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394642 | |||||||
chr3:160394756 | GA | G | 26 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0056 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.-47+4389delT | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160394756 | |||||||
chr3:160395036 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+4110A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395036 | |||||||
chr3:160395329 | T | C | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+3817A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395329 | |||||||
chr3:160395429 | T | C | 15 | a0002c0002t0001g0033 a0002c0002t0002g0003 a0002c0002t0002g0032 others(12): Show |
17 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+3717A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395429 | |||||||
chr3:160395672 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-47+3474C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395672 | |||||||
chr3:160395681 | A | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-47+3465T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395681 | |||||||
chr3:160395966 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-47+3180C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160395966 | |||||||
chr3:160396032 | G | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+3114C>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396032 | |||||||
chr3:160396056 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-47+3090A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396056 | |||||||
chr3:160396223 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-47+2923A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396223 | |||||||
chr3:160396345 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2801A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396345 | |||||||
chr3:160396346 | C | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2800G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396346 | |||||||
chr3:160396346 | CAT | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(29): Show |
33 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47+2798_-47+2799d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396346 | |||||||
chr3:160396347 | A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2799T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396347 | |||||||
chr3:160396360 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2786A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396360 | |||||||
chr3:160396369 | T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2777A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396369 | |||||||
chr3:160396384 | T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2762A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396384 | |||||||
chr3:160396398 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2748A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396398 | |||||||
chr3:160396399 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2747A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396399 | |||||||
chr3:160396404 | A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2742T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396404 | |||||||
chr3:160396409 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2737A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396409 | |||||||
chr3:160396410 | T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2736A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396410 | |||||||
chr3:160396413 | T | A | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2733A>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396413 | |||||||
chr3:160396419 | A | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2727T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396419 | |||||||
chr3:160396422 | T | G | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2724A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396422 | |||||||
chr3:160396430 | G | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2716C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396430 | |||||||
chr3:160396435 | T | C | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2711A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396435 | |||||||
chr3:160396436 | C | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2710G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396436 | |||||||
chr3:160396458 | G | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2688C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396458 | |||||||
chr3:160396461 | A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2685T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396461 | |||||||
chr3:160396481 | A | T | 1 | a0002c0002t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-47+2665T>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396481 | |||||||
chr3:160396547 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+2599G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396547 | |||||||
chr3:160396775 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47+2371A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160396775 | |||||||
chr3:160397035 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+2111A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397035 | |||||||
chr3:160397177 | CCA | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(19): Show |
24 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47+1967_-47+1968d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397177 | |||||||
chr3:160397216 | C | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-47+1930G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397216 | |||||||
chr3:160397586 | T | C | 2 | a0002c0002t0001g0084 a0002c0002t0001g0085 |
2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-47+1560A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397586 | |||||||
chr3:160397716 | C | CT | 59 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0175 others(56): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-47+1429dupA | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | |||||||
chr3:160397716 | C | CTT | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
18 | HG00642.hp2 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+1428_-47+1429d others(4): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | |||||||
chr3:160397716 | C | CTTT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
26 | HG00099.hp2 HG01243.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.-47+1427_-47+1429d others(5): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | |||||||
chr3:160397716 | C | CTTTT | 11 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0023 others(8): Show |
11 | HG01255.hp2 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+1426_-47+1429d others(6): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | |||||||
chr3:160397716 | CTTTTT | C | 5 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0002g0203 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1425_-47+1429d others(7): Show |
IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397716 | |||||||
chr3:160397724 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-47+1422A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397724 | |||||||
chr3:160397744 | G | T | 5 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1402C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397744 | |||||||
chr3:160397821 | A | C | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-47+1325T>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397821 | |||||||
chr3:160397980 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-47+1166G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160397980 | |||||||
chr3:160398046 | T | C | 9 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+1100A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398046 | |||||||
chr3:160398194 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-47+952T>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398194 | |||||||
chr3:160398381 | C | A | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+765G>T | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398381 | |||||||
chr3:160398386 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0001g0162 others(5): Show |
9 | HG01433.hp1 HG02257.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+760A>G | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398386 | |||||||
chr3:160398414 | G | T | 1 | a0002c0002t0002g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-47+732C>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398414 | |||||||
chr3:160398587 | C | T | 1 | a0002c0006t0002g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-47+559G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398587 | |||||||
chr3:160398964 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG00099.hp2 HG02976.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+182G>A | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160398964 | |||||||
chr3:160399019 | T | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-47+127A>C | IFT80 | ENSG00000068885.15 | transcript | ENST00000326448.12 | protein_coding | 1/19 | chr3 | 160399019 |