Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79989 |
| ensemblid | ENSG00000105948.13 |
| hgncid | 21882 |
| symbol | IFT56 |
| name | intraflagellar transport 56 |
| refseq_nuc | NM_024926.4 |
| refseq_prot | NP_079202.2 |
| ensembl_nuc | ENST00000464848.5 |
| ensembl_prot | ENSP00000419279.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 139133778 |
| end | 139191986 |
| strand | + |
| ver | v1.2 |
| region | chr7:139133778-139191986 |
| region5000 | chr7:139128778-139196986 |
| regionname0 | IFT56_chr7_139133778_139191986 |
| regionname5000 | IFT56_chr7_139128778_139196986 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 554 | 327 | 88 | 40 | 151 | 8 | 38 | 115 | IFT56_chr7_139128778_139196986 | IFT56 | MMLSR others(549): Show |
chr7 | 139128778 | 139196986 |
| a0002 | 0/0 | 554 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | MMLSR others(549): Show |
chr7 | 139128778 | 139196986 |
| a0003 | 0/0 | 554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | MMLSR others(549): Show |
chr7 | 139128778 | 139196986 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1662 | 286 | 73 | 39 | 127 | 8 | 37 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 | ||
| a0001c0002 | 0/0 | 1662 | 34 | 12 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 | ||
| a0001c0003 | 0/0 | 1662 | 4 | 3 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 | ||
| a0001c0004 | 0/0 | 1662 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 | ||
| a0002c0005 | 0/0 | 1662 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 | ||
| a0003c0006 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | ATGAT others(1657): Show |
chr7 | 139128778 | 139196986 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4299 | 97 | 32 | 12 | 39 | 1 | 13 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0002 | 0/1 | 4299 | 94 | 19 | 15 | 40 | 4 | 15 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0003 | 0/0 | 4299 | 64 | 7 | 2 | 47 | 1 | 7 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0005 | 0/0 | 4299 | 6 | 0 | 4 | 0 | 1 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0006 | 0/0 | 4293 | 6 | 6 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4288): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0007 | 1/0 | 4299 | 6 | 1 | 3 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0008 | 0/0 | 4299 | 3 | 0 | 2 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0010 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0011 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0012 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0013 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4288): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0014 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0016 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0017 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0001t0018 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0002t0001 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0002t0002 | 0/0 | 4299 | 7 | 7 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0002t0004 | 0/0 | 4299 | 22 | 0 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0003t0009 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0003t0015 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0001c0004t0001 | 0/0 | 4299 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0002c0005t0001 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| a0003c0006t0003 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | AGAAC others(4294): Show |
chr7 | 139128778 | 139196986 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0003 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0001 | 0/0 | 9 | 1 | 0 | 5 | 1 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0009 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0014g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0003t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0003t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0003t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0003t0015g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0002c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0002c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| a0003c0006t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0204 | EUR | GBR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | FIN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0227 | EUR | FIN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00544 | hp2 | a0002 | c0005 | t0001 | g0083 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00609 | hp2 | a0002 | c0005 | t0001 | g0002 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0122 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0117 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0173 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0176 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01891 | hp2 | a0001 | c0001 | t0018 | g0047 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02280 | hp2 | a0001 | c0003 | t0009 | g0109 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0041 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0219 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02615 | hp2 | a0001 | c0003 | t0009 | g0111 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0143 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0145 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03098 | hp1 | a0001 | c0003 | t0009 | g0108 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0144 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0169 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03834 | hp1 | a0001 | c0003 | t0015 | g0112 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0178 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18951 | hp2 | a0003 | c0006 | t0003 | g0265 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0078 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18964 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18975 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18983 | hp1 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18984 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18986 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18987 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0156 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19003 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19004 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19056 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ASW | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0214 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0183 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0151 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0249 | REF | REF | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0246 | REF | REF | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:139137853 | C | T | 1 | a0002 | 2 | HG00544.hp2 HG00609.hp2 |
missense_variant | MODERATE | c.148C>T | p.Arg50Cys | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/18 | 228/4299 | 148/1665 | 50/554 | chr7 | 139137853 | |||
| chr7:139165228 | C | T | 1 | a0003 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.889C>T | p.Arg297Cys | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/18 | 969/4299 | 889/1665 | 297/554 | chr7 | 139165228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:139134699 | C | T | 1 | a0001c0002 | 34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
synonymous_variant | LOW | c.48C>T | p.His16His | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/18 | 128/4299 | 48/1665 | 16/554 | chr7 | 139134699 | |||
| chr7:139178556 | C | G | 1 | a0001c0004 | 3 | NA19003.hp1 NA19010.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.1200C>G | p.Ala400Ala | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/18 | 1280/4299 | 1200/1665 | 400/554 | chr7 | 139178556 | |||
| chr7:139189342 | C | T | 1 | a0001c0003 | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.1575C>T | p.Leu525Leu | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1655/4299 | 1575/1665 | 525/554 | chr7 | 139189342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:139189445 | G | A | 1 | a0001c0002t0004 | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*13G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 13 | chr7 | 139189445 | ||||||
| chr7:139189670 | C | G | 2 | a0001c0001t0003 a0003c0006t0003 |
65 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 238 | chr7 | 139189670 | ||||||
| chr7:139189975 | G | C | 6 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(3): Show |
114 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 543 | chr7 | 139189975 | ||||||
| chr7:139190071 | G | T | 1 | a0001c0001t0018 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 639 | chr7 | 139190071 | ||||||
| chr7:139190106 | T | C | 6 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(3): Show |
114 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*674T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 674 | chr7 | 139190106 | ||||||
| chr7:139190221 | AGTTTTT | A | 2 | a0001c0001t0006 a0001c0001t0013 |
7 | HG02257.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*798delTTTGTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | INFO_REALIGN_3_PRIME | chr7 | 139190221 | |||||
| chr7:139190222 | GTTT | G | 3 | a0001c0001t0010 a0001c0001t0018 a0001c0002t0002 |
5 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*795delTTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | INFO_REALIGN_3_PRIME | chr7 | 139190222 | |||||
| chr7:139190225 | T | G | 2 | a0001c0001t0002 a0001c0002t0002 |
14 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | chr7 | 139190225 | ||||||
| chr7:139190225 | TTTG | T | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(6): Show |
180 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*828delGTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 826 | INFO_REALIGN_3_PRIME | chr7 | 139190225 | |||||
| chr7:139190243 | G | T | 1 | a0001c0001t0018 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 811 | chr7 | 139190243 | ||||||
| chr7:139190313 | T | G | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0013 others(1): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 881 | chr7 | 139190313 | ||||||
| chr7:139190391 | A | G | 1 | a0001c0003t0009 | 3 | HG02280.hp2 HG02615.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 959 | chr7 | 139190391 | ||||||
| chr7:139190401 | G | A | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
323 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*969G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 969 | chr7 | 139190401 | ||||||
| chr7:139190944 | G | A | 1 | a0001c0001t0013 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1512 | chr7 | 139190944 | ||||||
| chr7:139191144 | A | T | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1712A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1712 | chr7 | 139191144 | ||||||
| chr7:139191239 | T | C | 1 | a0001c0001t0011 | 2 | HG02622.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1807T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1807 | chr7 | 139191239 | ||||||
| chr7:139191586 | A | G | 1 | a0001c0001t0005 | 6 | HG00642.hp1 HG01070.hp1 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2154A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2154 | chr7 | 139191586 | ||||||
| chr7:139191603 | C | G | 1 | a0001c0001t0018 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2171C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2171 | chr7 | 139191603 | ||||||
| chr7:139191603 | C | T | 1 | a0001c0001t0016 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2171C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2171 | chr7 | 139191603 | ||||||
| chr7:139191613 | C | T | 1 | a0001c0001t0012 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2181C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2181 | chr7 | 139191613 | ||||||
| chr7:139191718 | A | G | 1 | a0001c0001t0008 | 3 | HG01243.hp1 HG01361.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2286A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2286 | chr7 | 139191718 | ||||||
| chr7:139191740 | G | C | 1 | a0001c0001t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2308 | chr7 | 139191740 | ||||||
| chr7:139191762 | T | C | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0013 |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2330T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2330 | chr7 | 139191762 | ||||||
| chr7:139191862 | T | G | 1 | a0001c0003t0015 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2430 | chr7 | 139191862 | ||||||
| chr7:139191894 | G | A | 1 | a0001c0001t0011 | 2 | HG02622.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2462G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2462 | chr7 | 139191894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:139133886 | G | A | 21 | a0001c0001t0018g0047 a0001c0002t0004g0011 a0001c0002t0004g0028 others(18): Show |
22 | HG01891.hp2 HG02015.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.3+26G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139133886 | |||||||
| chr7:139133998 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(129): Show |
154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.3+138G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139133998 | |||||||
| chr7:139134122 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3+262C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134122 | |||||||
| chr7:139134188 | C | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+328C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134188 | |||||||
| chr7:139134273 | AT | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.4-366delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 139134273 | ||||||
| chr7:139134395 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-260C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134395 | |||||||
| chr7:139134416 | G | A | 9 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4-239G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134416 | |||||||
| chr7:139134545 | G | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4-110G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134545 | |||||||
| chr7:139134856 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.141+64G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134856 | |||||||
| chr7:139134864 | T | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.141+72T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134864 | |||||||
| chr7:139134955 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+163G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134955 | |||||||
| chr7:139134997 | T | G | 2 | a0001c0001t0006g0146 a0001c0001t0013g0145 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.141+205T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134997 | |||||||
| chr7:139135050 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.141+258A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135050 | |||||||
| chr7:139135082 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.141+290C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135082 | |||||||
| chr7:139135211 | G | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
12 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.141+419G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135211 | |||||||
| chr7:139135273 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141+481G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135273 | |||||||
| chr7:139135277 | C | CA | 22 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0165 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+506dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | ||||||
| chr7:139135277 | CA | C | 7 | a0001c0001t0002g0257 a0001c0001t0003g0258 a0001c0001t0003g0260 others(4): Show |
7 | HG02155.hp2 HG03130.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+506delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | ||||||
| chr7:139135277 | CAA | C | 7 | a0001c0001t0003g0010 a0001c0001t0003g0264 a0001c0001t0003g0266 others(4): Show |
9 | HG00438.hp2 HG02056.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+505_141+506del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | ||||||
| chr7:139135293 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.141+501A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135293 | |||||||
| chr7:139135294 | A | C | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+502A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135294 | |||||||
| chr7:139135294 | AAAAAC | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.141+513_141+517del others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135294 | ||||||
| chr7:139135295 | AAAAC | A | 42 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0060 others(39): Show |
44 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(41): Show |
intron_variant | MODIFIER | c.141+507_141+510del others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135295 | ||||||
| chr7:139135298 | A | C | 1 | a0001c0001t0002g0207 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.141+506A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135298 | |||||||
| chr7:139135298 | AC | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(22): Show |
29 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+507delC | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135298 | |||||||
| chr7:139135299 | C | A | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0121 others(7): Show |
10 | HG00642.hp1 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+507C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135299 | |||||||
| chr7:139135299 | CAAA | C | 3 | a0001c0002t0001g0138 a0001c0002t0004g0028 a0001c0002t0004g0029 |
3 | HG03098.hp2 NA18977.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.141+509_141+511del others(3): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135299 | ||||||
| chr7:139135301 | A | C | 2 | a0001c0001t0006g0146 a0001c0001t0013g0145 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.141+509A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135301 | |||||||
| chr7:139135302 | A | C | 29 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0001c0002t0001g0141 others(26): Show |
30 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.141+510A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135302 | |||||||
| chr7:139135318 | T | C | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+526T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135318 | |||||||
| chr7:139135322 | G | A | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+530G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135322 | |||||||
| chr7:139135424 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.141+632T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135424 | |||||||
| chr7:139135499 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+707G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135499 | |||||||
| chr7:139135678 | T | A | 1 | a0001c0001t0002g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.141+886T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135678 | |||||||
| chr7:139135915 | C | CT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(98): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.141+1133dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135915 | ||||||
| chr7:139136074 | C | A | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+1282C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136074 | |||||||
| chr7:139136326 | C | A | 1 | a0001c0001t0003g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.142-1521C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136326 | |||||||
| chr7:139136432 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-1415C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136432 | |||||||
| chr7:139136637 | TTG | T | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1197_142-1196d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139136637 | ||||||
| chr7:139136676 | C | T | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-1171C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136676 | |||||||
| chr7:139136794 | C | T | 5 | a0001c0001t0002g0182 a0001c0001t0002g0253 a0001c0001t0002g0254 others(2): Show |
5 | HG02165.hp2 HG02602.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1053C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136794 | |||||||
| chr7:139136856 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.142-991G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136856 | |||||||
| chr7:139137065 | C | T | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0250 others(2): Show |
5 | HG02027.hp2 HG02040.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-782C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137065 | |||||||
| chr7:139137484 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-363C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137484 | |||||||
| chr7:139137758 | T | TGTTC | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.142-87_142-86insTC others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139137758 | ||||||
| chr7:139137797 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-50G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137797 | |||||||
| chr7:139137989 | A | G | 28 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0002t0001g0138 others(25): Show |
29 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.234+50A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139137989 | |||||||
| chr7:139138016 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.234+77A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138016 | |||||||
| chr7:139138149 | A | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.234+210A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138149 | |||||||
| chr7:139138185 | A | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.234+246A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138185 | |||||||
| chr7:139138485 | C | T | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+546C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138485 | |||||||
| chr7:139138503 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+564C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138503 | |||||||
| chr7:139138523 | T | C | 5 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+584T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138523 | |||||||
| chr7:139138533 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.234+594G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138533 | |||||||
| chr7:139138567 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.234+628C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138567 | |||||||
| chr7:139138811 | C | CT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(98): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+889dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139138811 | ||||||
| chr7:139138811 | C | CTT | 25 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0002t0001g0138 others(22): Show |
26 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+888_234+889dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139138811 | ||||||
| chr7:139138874 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0179 |
3 | HG02735.hp1 HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.234+935G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138874 | |||||||
| chr7:139138972 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.235-918G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138972 | |||||||
| chr7:139139034 | G | A | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-856G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139034 | |||||||
| chr7:139139089 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.235-801G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139089 | |||||||
| chr7:139139091 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.235-799C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139091 | |||||||
| chr7:139139166 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(142): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-724G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139166 | |||||||
| chr7:139139299 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.235-591C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139299 | |||||||
| chr7:139139403 | A | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235-487A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139403 | |||||||
| chr7:139139627 | C | A | 1 | a0001c0001t0002g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.235-263C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139627 | |||||||
| chr7:139139658 | T | C | 2 | a0001c0001t0006g0146 a0001c0001t0013g0145 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.235-232T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139658 | |||||||
| chr7:139139692 | G | T | 1 | a0001c0003t0015g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.235-198G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139692 | |||||||
| chr7:139139700 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.235-190T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139700 | |||||||
| chr7:139140096 | GA | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.349+102delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140096 | ||||||
| chr7:139140103 | A | G | 27 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0001g0138 others(24): Show |
28 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+99A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140103 | |||||||
| chr7:139140128 | A | G | 28 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0001g0138 others(25): Show |
29 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(26): Show |
intron_variant | MODIFIER | c.349+124A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140128 | |||||||
| chr7:139140162 | G | GTAAC | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+161_349+164dup others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140162 | ||||||
| chr7:139140243 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.349+239G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140243 | |||||||
| chr7:139140440 | G | C | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.349+436G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140440 | |||||||
| chr7:139140458 | T | TTAAAAA | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.349+457_349+458ins others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140458 | ||||||
| chr7:139140462 | G | A | 1 | a0001c0002t0002g0131 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.349+458G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140462 | |||||||
| chr7:139140699 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.349+695C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140699 | |||||||
| chr7:139140700 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349+696G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140700 | |||||||
| chr7:139140731 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.349+727C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140731 | |||||||
| chr7:139140775 | C | CA | 124 | a0001c0001t0001g0051 a0001c0001t0001g0110 a0001c0001t0002g0001 others(121): Show |
155 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.349+794dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140775 | C | CAA | 29 | a0001c0001t0001g0129 a0001c0001t0002g0049 a0001c0001t0002g0160 others(26): Show |
29 | HG01175.hp1 HG01891.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.349+793_349+794dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140775 | C | CAAA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(35): Show |
44 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.349+792_349+794dup others(3): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140775 | C | CAAAA | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0118 others(4): Show |
7 | HG00438.hp1 HG01175.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+791_349+794dup others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140775 | CAA | C | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+793_349+794del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140775 | CAAAAAAA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349+788_349+794del others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | ||||||
| chr7:139140832 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+828G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140832 | |||||||
| chr7:139140948 | A | G | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+944A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140948 | |||||||
| chr7:139140951 | C | CTTTTTTT others(2685): Show |
1 | a0001c0001t0001g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+959_349+960ins others(2692): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0002g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2686): Show |
1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2693): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2688): Show |
1 | a0001c0001t0002g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2695): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0002g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2687): Show |
3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0057 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0002g0055 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0002g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140951 | CT | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.349+961delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | ||||||
| chr7:139140965 | T | C | 3 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 |
3 | HG03041.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.349+961T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140965 | |||||||
| chr7:139140966 | A | T | 5 | a0001c0001t0001g0110 a0001c0003t0009g0108 a0001c0003t0009g0109 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+962A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140966 | |||||||
| chr7:139141183 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-1073C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141183 | |||||||
| chr7:139141191 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.350-1065G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141191 | |||||||
| chr7:139141193 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1063G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141193 | |||||||
| chr7:139141218 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.350-1038G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141218 | |||||||
| chr7:139141256 | GA | G | 11 | a0001c0001t0002g0248 a0001c0001t0006g0146 a0001c0001t0006g0147 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-984delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139141256 | ||||||
| chr7:139141256 | GAA | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.350-985_350-984del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139141256 | ||||||
| chr7:139141265 | A | G | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-991A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141265 | |||||||
| chr7:139141275 | CAG | C | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 |
3 | NA18944.hp2 NA18955.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.350-980_350-979del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141275 | |||||||
| chr7:139141407 | C | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.350-849C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141407 | |||||||
| chr7:139141467 | G | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.350-789G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141467 | |||||||
| chr7:139141499 | A | C | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-757A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141499 | |||||||
| chr7:139141558 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.350-698G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141558 | |||||||
| chr7:139141764 | G | A | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.350-492G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141764 | |||||||
| chr7:139141951 | C | T | 9 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0032 others(6): Show |
9 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-305C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141951 | |||||||
| chr7:139142167 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.350-89G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139142167 | |||||||
| chr7:139142489 | C | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+184C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142489 | |||||||
| chr7:139142552 | T | TG | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+249dupG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139142552 | ||||||
| chr7:139142567 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+262C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142567 | |||||||
| chr7:139142781 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.399+476G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142781 | |||||||
| chr7:139142862 | A | G | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.399+557A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142862 | |||||||
| chr7:139142944 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+639T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142944 | |||||||
| chr7:139143084 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+779G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143084 | |||||||
| chr7:139143171 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.399+866C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143171 | |||||||
| chr7:139143426 | CAT | C | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1126_399+1127d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139143426 | ||||||
| chr7:139143689 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+1384A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143689 | |||||||
| chr7:139143719 | A | T | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1414A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143719 | |||||||
| chr7:139143751 | C | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+1446C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143751 | |||||||
| chr7:139143805 | A | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+1500A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143805 | |||||||
| chr7:139143842 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0258 |
3 | NA18955.hp2 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.399+1537T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143842 | |||||||
| chr7:139143944 | C | G | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.399+1639C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143944 | |||||||
| chr7:139143995 | A | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.399+1690A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143995 | |||||||
| chr7:139144037 | T | C | 5 | a0001c0001t0001g0110 a0001c0003t0009g0108 a0001c0003t0009g0109 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+1732T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144037 | |||||||
| chr7:139144187 | G | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0002t0001g0138 others(4): Show |
7 | HG02109.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+1882G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144187 | |||||||
| chr7:139144350 | A | C | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.399+2045A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144350 | |||||||
| chr7:139144360 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0060 a0001c0001t0001g0061 |
4 | HG03471.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+2055T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144360 | |||||||
| chr7:139144379 | T | G | 1 | a0001c0002t0004g0030 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.399+2074T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144379 | |||||||
| chr7:139144597 | A | ATATG | 23 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0105 others(20): Show |
28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.399+2311_399+2314d others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139144597 | ||||||
| chr7:139144699 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+2394A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144699 | |||||||
| chr7:139144719 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.399+2414C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144719 | |||||||
| chr7:139144741 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.400-2404C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144741 | |||||||
| chr7:139145016 | A | C | 2 | a0001c0001t0003g0241 a0001c0001t0003g0242 |
2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.400-2129A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145016 | |||||||
| chr7:139145295 | T | C | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.400-1850T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145295 | |||||||
| chr7:139145332 | G | A | 1 | a0001c0001t0017g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-1813G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145332 | |||||||
| chr7:139145380 | GTCT | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.400-1762_400-1760d others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139145380 | ||||||
| chr7:139145461 | G | A | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-1684G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145461 | |||||||
| chr7:139145470 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-1675G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145470 | |||||||
| chr7:139145510 | T | C | 35 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0002t0001g0138 others(32): Show |
36 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.400-1635T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145510 | |||||||
| chr7:139145583 | C | G | 5 | a0001c0001t0001g0110 a0001c0003t0009g0108 a0001c0003t0009g0109 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-1562C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145583 | |||||||
| chr7:139145585 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-1560C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145585 | |||||||
| chr7:139145586 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(126): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.400-1559A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145586 | |||||||
| chr7:139145691 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-1454T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145691 | |||||||
| chr7:139146161 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.400-984A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146161 | |||||||
| chr7:139146537 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.400-608G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146537 | |||||||
| chr7:139146735 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.400-410C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146735 | |||||||
| chr7:139146766 | C | CA | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(108): Show |
139 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.400-361dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | ||||||
| chr7:139146766 | C | CAA | 33 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0106 others(30): Show |
34 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.400-362_400-361dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | ||||||
| chr7:139146766 | CA | C | 13 | a0001c0001t0002g0168 a0001c0001t0003g0192 a0001c0001t0003g0240 others(10): Show |
13 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-361delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | ||||||
| chr7:139146961 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-184C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146961 | |||||||
| chr7:139146976 | C | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0058 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.400-169C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146976 | |||||||
| chr7:139147080 | A | G | 5 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-65A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139147080 | |||||||
| chr7:139147361 | T | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+71T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147361 | |||||||
| chr7:139147455 | T | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.545+165T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147455 | |||||||
| chr7:139147721 | G | A | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.545+431G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147721 | |||||||
| chr7:139147892 | C | T | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-314C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147892 | |||||||
| chr7:139148190 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.546-16T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139148190 | |||||||
| chr7:139148660 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.717+283C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148660 | |||||||
| chr7:139148691 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(208): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.717+314A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148691 | |||||||
| chr7:139148817 | G | C | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+440G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148817 | |||||||
| chr7:139148818 | G | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+441G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148818 | |||||||
| chr7:139148822 | G | A | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+445G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148822 | |||||||
| chr7:139148887 | C | T | 2 | a0001c0002t0002g0130 a0001c0002t0002g0132 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.717+510C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148887 | |||||||
| chr7:139149133 | A | G | 1 | a0001c0002t0002g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.717+756A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149133 | |||||||
| chr7:139149135 | C | T | 7 | a0001c0001t0006g0147 a0001c0001t0006g0148 a0001c0001t0006g0149 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+758C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149135 | |||||||
| chr7:139149191 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+814G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149191 | |||||||
| chr7:139149230 | G | A | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+853G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149230 | |||||||
| chr7:139149304 | C | CA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
112 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.717+943dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | ||||||
| chr7:139149304 | CA | C | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0002g0221 others(7): Show |
10 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.717+943delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | ||||||
| chr7:139149304 | CAA | C | 20 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(17): Show |
21 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.717+942_717+943del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | ||||||
| chr7:139149458 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.717+1081C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149458 | |||||||
| chr7:139149563 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.717+1186T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149563 | |||||||
| chr7:139149584 | C | G | 20 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(17): Show |
21 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.717+1207C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149584 | |||||||
| chr7:139149765 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.717+1388G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149765 | |||||||
| chr7:139149779 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+1402C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149779 | |||||||
| chr7:139149884 | A | G | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+1507A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149884 | |||||||
| chr7:139149906 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(25): Show |
33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.717+1529A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149906 | |||||||
| chr7:139150564 | A | G | 1 | a0001c0001t0006g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+2187A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150564 | |||||||
| chr7:139150596 | G | A | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.717+2219G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150596 | |||||||
| chr7:139150734 | A | G | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.717+2357A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150734 | |||||||
| chr7:139150769 | G | A | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.717+2392G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150769 | |||||||
| chr7:139151141 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.717+2764A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151141 | |||||||
| chr7:139151148 | G | T | 1 | a0001c0003t0009g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.717+2771G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151148 | |||||||
| chr7:139151602 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.717+3225T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151602 | |||||||
| chr7:139151629 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.717+3252A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151629 | |||||||
| chr7:139151731 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+3354G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151731 | |||||||
| chr7:139151804 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.717+3427G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151804 | |||||||
| chr7:139151870 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+3493T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151870 | |||||||
| chr7:139152017 | C | T | 1 | a0001c0002t0002g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.717+3640C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152017 | |||||||
| chr7:139152061 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.717+3684C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152061 | |||||||
| chr7:139152268 | A | C | 2 | a0001c0001t0003g0200 a0001c0001t0003g0239 |
2 | NA18940.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.717+3891A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152268 | |||||||
| chr7:139152420 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.717+4043C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152420 | |||||||
| chr7:139152781 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.717+4404G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152781 | |||||||
| chr7:139152878 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.717+4501G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152878 | |||||||
| chr7:139153097 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0052 others(5): Show |
8 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+4720C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153097 | |||||||
| chr7:139153151 | G | GA | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(137): Show |
164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.717+4788dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139153151 | ||||||
| chr7:139153207 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+4830T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153207 | |||||||
| chr7:139153446 | C | CA | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(128): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.717+5083dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139153446 | ||||||
| chr7:139153446 | C | T | 1 | a0001c0001t0007g0259 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.717+5069C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153446 | |||||||
| chr7:139153549 | C | A | 1 | a0001c0001t0003g0222 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.717+5172C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153549 | |||||||
| chr7:139153708 | C | G | 1 | a0001c0001t0007g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.717+5331C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153708 | |||||||
| chr7:139153743 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.717+5366A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153743 | |||||||
| chr7:139153781 | G | A | 27 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0001g0138 others(24): Show |
28 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+5404G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153781 | |||||||
| chr7:139153878 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0110 others(23): Show |
31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.717+5501A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153878 | |||||||
| chr7:139153881 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+5504G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153881 | |||||||
| chr7:139153933 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.717+5556G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153933 | |||||||
| chr7:139154340 | A | G | 1 | a0001c0001t0006g0153 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.717+5963A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154340 | |||||||
| chr7:139154353 | C | CT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0051 others(71): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.717+5990dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154353 | ||||||
| chr7:139154353 | CT | C | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+5990delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154353 | ||||||
| chr7:139154392 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.717+6015G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154392 | |||||||
| chr7:139154411 | T | C | 1 | a0001c0002t0004g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.717+6034T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154411 | |||||||
| chr7:139154665 | C | A | 1 | a0001c0001t0002g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.718-6283C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154665 | |||||||
| chr7:139154680 | C | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(10): Show |
16 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.718-6268C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154680 | |||||||
| chr7:139154686 | C | T | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.718-6262C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154686 | |||||||
| chr7:139154819 | G | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-6129G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154819 | |||||||
| chr7:139154830 | A | G | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-6118A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154830 | |||||||
| chr7:139154966 | G | GTTTTTTT | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5977_718-5976i others(9): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154966 | ||||||
| chr7:139154972 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5976C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154972 | |||||||
| chr7:139154973 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5975C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154973 | |||||||
| chr7:139155095 | C | T | 1 | a0001c0002t0004g0045 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.718-5853C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155095 | |||||||
| chr7:139155316 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-5632C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155316 | |||||||
| chr7:139155457 | T | G | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-5491T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155457 | |||||||
| chr7:139155525 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-5423A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155525 | |||||||
| chr7:139155532 | A | G | 2 | a0001c0001t0003g0181 a0001c0001t0003g0252 |
2 | NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.718-5416A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155532 | |||||||
| chr7:139155751 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.718-5197T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155751 | |||||||
| chr7:139155773 | G | A | 6 | a0001c0001t0003g0200 a0001c0001t0003g0223 a0001c0001t0003g0239 others(3): Show |
6 | NA18940.hp2 NA18944.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-5175G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155773 | |||||||
| chr7:139155773 | G | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.718-5175G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155773 | |||||||
| chr7:139156362 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.718-4586C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156362 | |||||||
| chr7:139156389 | CT | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-4549delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139156389 | ||||||
| chr7:139156423 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0110 others(23): Show |
31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.718-4525T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156423 | |||||||
| chr7:139156463 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0093 |
2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.718-4485A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156463 | |||||||
| chr7:139156499 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0110 others(23): Show |
31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.718-4449C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156499 | |||||||
| chr7:139156611 | C | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(123): Show |
150 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.718-4337C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156611 | |||||||
| chr7:139156784 | A | T | 5 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0234 others(2): Show |
5 | NA18939.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-4164A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156784 | |||||||
| chr7:139156845 | C | T | 1 | a0001c0001t0011g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.718-4103C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156845 | |||||||
| chr7:139156982 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-3966C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156982 | |||||||
| chr7:139157058 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-3890G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157058 | |||||||
| chr7:139157139 | C | CT | 126 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0001t0001g0128 others(123): Show |
157 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.718-3785dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157139 | CTT | C | 16 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(13): Show |
16 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-3786_718-3785d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157139 | CTTT | C | 29 | a0001c0002t0001g0142 a0001c0002t0002g0130 a0001c0002t0002g0131 others(26): Show |
30 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.718-3787_718-3785d others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157139 | CTTTTTTT others(2): Show |
C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.718-3793_718-3785d others(11): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157139 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.718-3794_718-3785d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157139 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0110 a0001c0003t0009g0108 a0001c0003t0009g0109 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-3798_718-3785d others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | ||||||
| chr7:139157146 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-3802T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157146 | |||||||
| chr7:139157249 | C | T | 1 | a0001c0002t0004g0044 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.718-3699C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157249 | |||||||
| chr7:139157290 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-3658A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157290 | |||||||
| chr7:139157306 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.718-3642C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157306 | |||||||
| chr7:139157495 | A | AT | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
106 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.718-3430dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | ||||||
| chr7:139157495 | A | ATT | 11 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
11 | HG01928.hp2 HG01952.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.718-3431_718-3430d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | ||||||
| chr7:139157495 | AT | A | 27 | a0001c0001t0002g0154 a0001c0001t0002g0203 a0001c0001t0002g0206 others(24): Show |
28 | HG00597.hp2 HG01070.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.718-3430delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | ||||||
| chr7:139157734 | G | A | 1 | a0001c0003t0009g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.718-3214G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157734 | |||||||
| chr7:139157769 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-3179A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157769 | |||||||
| chr7:139157819 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.718-3129T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157819 | |||||||
| chr7:139157949 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2999G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157949 | |||||||
| chr7:139158114 | C | T | 4 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2834C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158114 | |||||||
| chr7:139158270 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.718-2678C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158270 | |||||||
| chr7:139158271 | G | A | 9 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0002g0130 others(6): Show |
9 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-2677G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158271 | |||||||
| chr7:139158313 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0055 others(1): Show |
4 | HG01943.hp2 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2633_718-2623d others(13): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(5): Show |
35 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0051 others(32): Show |
40 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.718-2634_718-2623d others(14): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(6): Show |
24 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0121 others(21): Show |
25 | HG00544.hp1 HG00642.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(15): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(7): Show |
4 | a0001c0002t0002g0133 a0001c0002t0004g0028 a0001c0002t0004g0034 others(1): Show |
4 | HG02258.hp1 HG02300.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0063 a0001c0001t0001g0088 a0001c0001t0001g0092 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(17): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(9): Show |
35 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(32): Show |
51 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(18): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(10): Show |
24 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(21): Show |
26 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(19): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158313 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.718-2623_718-2622i others(20): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | ||||||
| chr7:139158391 | T | C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0136 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.718-2557T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158391 | |||||||
| chr7:139158783 | G | A | 5 | a0001c0001t0002g0170 a0001c0001t0002g0177 a0001c0001t0002g0193 others(2): Show |
5 | HG02647.hp1 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-2165G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158783 | |||||||
| chr7:139158787 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-2161A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158787 | |||||||
| chr7:139158833 | G | C | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2115G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158833 | |||||||
| chr7:139158871 | G | A | 8 | a0001c0001t0002g0168 a0001c0002t0002g0130 a0001c0002t0002g0131 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2077G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158871 | |||||||
| chr7:139158941 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0002g0160 |
2 | HG01928.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-2007G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158941 | |||||||
| chr7:139159149 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-1799A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159149 | |||||||
| chr7:139159201 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.718-1747G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159201 | |||||||
| chr7:139159222 | A | T | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.718-1726A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159222 | |||||||
| chr7:139159417 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
141 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.718-1531G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159417 | |||||||
| chr7:139159501 | G | A | 7 | a0001c0001t0006g0147 a0001c0001t0006g0148 a0001c0001t0006g0149 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1447G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159501 | |||||||
| chr7:139159956 | C | T | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-992C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159956 | |||||||
| chr7:139159981 | G | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0120 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-967G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159981 | |||||||
| chr7:139160017 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.718-931A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160017 | |||||||
| chr7:139160123 | A | T | 7 | a0001c0001t0003g0200 a0001c0001t0003g0223 a0001c0001t0003g0230 others(4): Show |
7 | NA18940.hp2 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-825A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160123 | |||||||
| chr7:139160433 | C | CT | 22 | a0001c0001t0006g0146 a0001c0002t0004g0011 a0001c0002t0004g0028 others(19): Show |
23 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(20): Show |
intron_variant | MODIFIER | c.718-498dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139160433 | ||||||
| chr7:139160433 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.718-498delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139160433 | ||||||
| chr7:139160618 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(176): Show |
210 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.718-330A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160618 | |||||||
| chr7:139160657 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.718-291C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160657 | |||||||
| chr7:139160683 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.718-265G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160683 | |||||||
| chr7:139160732 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-216G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160732 | |||||||
| chr7:139160742 | A | T | 1 | a0001c0002t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718-206A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160742 | |||||||
| chr7:139161186 | T | A | 28 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0001g0138 others(25): Show |
29 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(26): Show |
intron_variant | MODIFIER | c.792+164T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161186 | |||||||
| chr7:139161510 | T | C | 10 | a0001c0001t0001g0051 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+488T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161510 | |||||||
| chr7:139161603 | G | T | 1 | a0001c0001t0002g0270 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.792+581G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161603 | |||||||
| chr7:139161731 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.792+709A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161731 | |||||||
| chr7:139161743 | T | C | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.792+721T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161743 | |||||||
| chr7:139161826 | A | C | 23 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0004g0011 others(20): Show |
24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.792+804A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161826 | |||||||
| chr7:139162145 | A | G | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.792+1123A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162145 | |||||||
| chr7:139162454 | C | G | 1 | a0001c0002t0004g0011 | 2 | NA18939.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.792+1432C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162454 | |||||||
| chr7:139162627 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.792+1605G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162627 | |||||||
| chr7:139162730 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.792+1708G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162730 | |||||||
| chr7:139162749 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0113 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.792+1727A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162749 | |||||||
| chr7:139162972 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.792+1950A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162972 | |||||||
| chr7:139162984 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0157 |
4 | HG00621.hp1 NA18747.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+1962G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162984 | |||||||
| chr7:139163111 | G | A | 23 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0004g0011 others(20): Show |
24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.793-2021G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163111 | |||||||
| chr7:139163141 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.793-1991G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163141 | |||||||
| chr7:139163296 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.793-1836C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163296 | |||||||
| chr7:139163329 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1803G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163329 | |||||||
| chr7:139163340 | T | TA | 5 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0070 others(2): Show |
6 | HG02451.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-1777dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 139163340 | ||||||
| chr7:139163673 | A | G | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793-1459A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163673 | |||||||
| chr7:139163856 | A | G | 23 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0004g0011 others(20): Show |
24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.793-1276A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163856 | |||||||
| chr7:139163967 | T | G | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793-1165T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163967 | |||||||
| chr7:139164054 | T | C | 8 | a0001c0001t0003g0189 a0001c0002t0002g0130 a0001c0002t0002g0131 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-1078T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164054 | |||||||
| chr7:139164055 | G | A | 5 | a0001c0001t0002g0170 a0001c0001t0002g0177 a0001c0001t0002g0193 others(2): Show |
5 | HG02647.hp1 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-1077G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164055 | |||||||
| chr7:139164470 | G | C | 1 | a0001c0002t0004g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.793-662G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164470 | |||||||
| chr7:139164537 | G | T | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-595G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164537 | |||||||
| chr7:139164575 | C | T | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.793-557C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164575 | |||||||
| chr7:139164796 | G | T | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-336G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164796 | |||||||
| chr7:139164939 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.793-193G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164939 | |||||||
| chr7:139165053 | T | C | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-79T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139165053 | |||||||
| chr7:139165275 | T | A | 2 | a0001c0001t0002g0207 a0001c0001t0002g0248 |
2 | HG02129.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.895+41T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165275 | |||||||
| chr7:139165579 | A | G | 2 | a0001c0001t0010g0151 a0001c0001t0010g0152 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.895+345A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165579 | |||||||
| chr7:139165903 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.895+669A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165903 | |||||||
| chr7:139166034 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.895+800C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166034 | |||||||
| chr7:139166168 | G | C | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-672G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166168 | |||||||
| chr7:139166221 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.896-619G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166221 | |||||||
| chr7:139166248 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
152 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.896-592G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166248 | |||||||
| chr7:139166419 | A | C | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.896-421A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166419 | |||||||
| chr7:139166517 | AAT | A | 51 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(48): Show |
52 | HG01943.hp2 HG02015.hp2 HG02071.hp1 others(49): Show |
intron_variant | MODIFIER | c.896-310_896-309del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139166517 | ||||||
| chr7:139166517 | AATAT | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.896-312_896-309del others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139166517 | ||||||
| chr7:139166556 | TG | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.896-283delG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166556 | |||||||
| chr7:139166633 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0214 |
2 | HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.896-207C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166633 | |||||||
| chr7:139166681 | A | G | 12 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.896-159A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166681 | |||||||
| chr7:139166775 | G | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0248 |
2 | HG02129.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.896-65G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166775 | |||||||
| chr7:139166968 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.951+73G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139166968 | |||||||
| chr7:139166969 | T | A | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.951+74T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139166969 | |||||||
| chr7:139167029 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.951+134A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167029 | |||||||
| chr7:139167426 | G | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.951+531G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167426 | |||||||
| chr7:139167605 | T | A | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.951+710T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167605 | |||||||
| chr7:139167703 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
115 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.952-641C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167703 | |||||||
| chr7:139167767 | C | T | 5 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.952-577C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167767 | |||||||
| chr7:139167839 | G | C | 1 | a0001c0003t0015g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.952-505G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167839 | |||||||
| chr7:139167876 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.952-468G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167876 | |||||||
| chr7:139167887 | G | A | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-457G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167887 | |||||||
| chr7:139167940 | CA | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(133): Show |
160 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.952-389delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 139167940 | ||||||
| chr7:139167980 | G | T | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.952-364G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167980 | |||||||
| chr7:139167984 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.952-360T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167984 | |||||||
| chr7:139168112 | T | C | 1 | a0001c0001t0005g0122 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.952-232T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168112 | |||||||
| chr7:139168149 | T | C | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-195T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168149 | |||||||
| chr7:139168217 | C | T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0258 |
3 | NA18955.hp2 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.952-127C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168217 | |||||||
| chr7:139168285 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.952-59T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168285 | |||||||
| chr7:139168569 | C | CA | 13 | a0001c0001t0002g0004 a0001c0001t0002g0027 a0001c0001t0002g0159 others(10): Show |
19 | HG00140.hp1 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1005+184dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139168569 | ||||||
| chr7:139168569 | CA | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(123): Show |
150 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1005+184delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139168569 | ||||||
| chr7:139168581 | AC | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+185delC | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168581 | |||||||
| chr7:139168582 | C | A | 1 | a0001c0001t0003g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1005+185C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168582 | |||||||
| chr7:139168754 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1005+357A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168754 | |||||||
| chr7:139168981 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1006-308G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168981 | |||||||
| chr7:139169208 | C | A | 1 | a0001c0001t0007g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1006-81C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139169208 | |||||||
| chr7:139169687 | C | T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1069+335C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169687 | |||||||
| chr7:139169757 | T | G | 22 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(19): Show |
23 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(20): Show |
intron_variant | MODIFIER | c.1069+405T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169757 | |||||||
| chr7:139169933 | G | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0208 a0001c0001t0002g0209 |
4 | HG00609.hp1 HG02083.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+581G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169933 | |||||||
| chr7:139169988 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(207): Show |
243 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1069+636T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169988 | |||||||
| chr7:139170463 | A | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0024 a0001c0001t0002g0025 others(8): Show |
18 | HG00609.hp1 HG00621.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+1111A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170463 | |||||||
| chr7:139170547 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+1195C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170547 | |||||||
| chr7:139170564 | TG | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(25): Show |
39 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1069+1215delG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139170564 | ||||||
| chr7:139170706 | A | C | 3 | a0001c0001t0008g0173 a0001c0001t0008g0176 a0001c0001t0008g0178 |
3 | HG01243.hp1 HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1069+1354A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170706 | |||||||
| chr7:139170930 | T | A | 1 | a0001c0001t0001g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069+1578T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170930 | |||||||
| chr7:139171034 | T | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+1682T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171034 | |||||||
| chr7:139171083 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
115 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1069+1731A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171083 | |||||||
| chr7:139171487 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1069+2135C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171487 | |||||||
| chr7:139171549 | T | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+2197T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171549 | |||||||
| chr7:139171588 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1069+2236A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171588 | |||||||
| chr7:139171684 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0128 |
3 | HG03017.hp1 HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1069+2332C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171684 | |||||||
| chr7:139171803 | G | A | 1 | a0001c0001t0011g0143 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1069+2451G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171803 | |||||||
| chr7:139171907 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1069+2555G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171907 | |||||||
| chr7:139172079 | C | A | 2 | a0001c0001t0006g0146 a0001c0001t0013g0145 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1069+2727C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172079 | |||||||
| chr7:139172144 | AATT | A | 33 | a0001c0001t0001g0114 a0001c0001t0011g0143 a0001c0001t0011g0144 others(30): Show |
34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+2794_1069+279 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172144 | ||||||
| chr7:139172144 | AATTAC | A | 10 | a0001c0001t0001g0086 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG00408.hp2 HG01943.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+2793_1069+279 others(9): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172144 | |||||||
| chr7:139172145 | ATTAC | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
115 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1069+2797_1069+280 others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172145 | ||||||
| chr7:139172149 | C | A | 33 | a0001c0001t0001g0114 a0001c0001t0011g0143 a0001c0001t0011g0144 others(30): Show |
34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+2797C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172149 | |||||||
| chr7:139172236 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1069+2884C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172236 | |||||||
| chr7:139172267 | TTCCTGCC others(24): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2916_1069+294 others(35): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172267 | |||||||
| chr7:139172299 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2947A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172299 | |||||||
| chr7:139172302 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2950T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172302 | |||||||
| chr7:139172330 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2978G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172330 | |||||||
| chr7:139172334 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2982A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172334 | |||||||
| chr7:139172335 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2983C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172335 | |||||||
| chr7:139172337 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2985A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172337 | |||||||
| chr7:139172340 | C | G | 3 | a0001c0004t0001g0079 a0001c0004t0001g0089 a0001c0004t0001g0091 |
3 | NA19003.hp1 NA19010.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1069+2988C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172340 | |||||||
| chr7:139172340 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2988C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172340 | |||||||
| chr7:139172341 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2989C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172341 | |||||||
| chr7:139172343 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2991A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172343 | |||||||
| chr7:139172344 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2992A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172344 | |||||||
| chr7:139172350 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2998T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172350 | |||||||
| chr7:139172351 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2999A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172351 | |||||||
| chr7:139172375 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+3023G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172375 | |||||||
| chr7:139172381 | C | CCTCTACA others(21): Show |
1 | a0001c0001t0001g0118 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+3033_1069+303 others(32): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172381 | ||||||
| chr7:139172463 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1069+3111C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172463 | |||||||
| chr7:139172527 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1069+3175G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172527 | |||||||
| chr7:139172563 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069+3211C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172563 | |||||||
| chr7:139172700 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1069+3348A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172700 | |||||||
| chr7:139172747 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1069+3395C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172747 | |||||||
| chr7:139173024 | G | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(134): Show |
161 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1069+3672G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173024 | |||||||
| chr7:139173136 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1069+3784C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173136 | |||||||
| chr7:139173145 | G | C | 1 | a0001c0001t0003g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1069+3793G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173145 | |||||||
| chr7:139173225 | C | CT | 10 | a0001c0001t0001g0084 a0001c0001t0001g0118 a0001c0001t0002g0172 others(7): Show |
10 | HG02451.hp2 HG02486.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+3892dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139173225 | ||||||
| chr7:139173268 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0057 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1069+3916C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173268 | |||||||
| chr7:139173330 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1069+3978C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173330 | |||||||
| chr7:139173464 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1069+4112G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173464 | |||||||
| chr7:139173524 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069+4172C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173524 | |||||||
| chr7:139173587 | G | T | 9 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069+4235G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173587 | |||||||
| chr7:139173665 | G | C | 1 | a0001c0001t0002g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1069+4313G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173665 | |||||||
| chr7:139174011 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): Show |
137 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1070-4203A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174011 | |||||||
| chr7:139174092 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1070-4122G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174092 | |||||||
| chr7:139174109 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1070-4105G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174109 | |||||||
| chr7:139174277 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1070-3937C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174277 | |||||||
| chr7:139174385 | G | A | 1 | a0001c0002t0004g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1070-3829G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174385 | |||||||
| chr7:139174403 | A | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0058 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1070-3811A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174403 | |||||||
| chr7:139174421 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1070-3793A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174421 | |||||||
| chr7:139174481 | G | A | 2 | a0001c0001t0006g0148 a0001c0001t0006g0153 |
2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1070-3733G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174481 | |||||||
| chr7:139174560 | ACAAT | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-3650_1070-364 others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139174560 | ||||||
| chr7:139174565 | C | A | 1 | a0001c0003t0015g0112 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1070-3649C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174565 | |||||||
| chr7:139174622 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1070-3592A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174622 | |||||||
| chr7:139174743 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0085 |
2 | HG02056.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1070-3471G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174743 | |||||||
| chr7:139174743 | G | C | 5 | a0001c0002t0004g0028 a0001c0002t0004g0029 a0001c0002t0004g0035 others(2): Show |
5 | NA18612.hp1 NA18940.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-3471G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174743 | |||||||
| chr7:139174807 | C | T | 2 | a0001c0001t0002g0182 a0001c0001t0002g0253 |
2 | NA18947.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1070-3407C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174807 | |||||||
| chr7:139174864 | T | C | 4 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-3350T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174864 | |||||||
| chr7:139174984 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1070-3230A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174984 | |||||||
| chr7:139175037 | AAAG | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1070-3174_1070-317 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139175037 | ||||||
| chr7:139175069 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1070-3145G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175069 | |||||||
| chr7:139175138 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-3076A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175138 | |||||||
| chr7:139175269 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-2945C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175269 | |||||||
| chr7:139176099 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1070-2115A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176099 | |||||||
| chr7:139176109 | G | A | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-2105G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176109 | |||||||
| chr7:139176111 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1070-2103A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176111 | |||||||
| chr7:139176170 | T | C | 23 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0004g0011 others(20): Show |
24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.1070-2044T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176170 | |||||||
| chr7:139176213 | GT | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1998delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139176213 | ||||||
| chr7:139176257 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-1957C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176257 | |||||||
| chr7:139176538 | A | C | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-1676A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176538 | |||||||
| chr7:139176696 | T | C | 7 | a0001c0001t0006g0147 a0001c0001t0006g0148 a0001c0001t0006g0149 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-1518T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176696 | |||||||
| chr7:139176812 | A | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0003g0240 others(1): Show |
6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070-1402A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176812 | |||||||
| chr7:139176901 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1070-1313C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176901 | |||||||
| chr7:139176949 | G | A | 9 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1265G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176949 | |||||||
| chr7:139176969 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-1245C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176969 | |||||||
| chr7:139177039 | G | C | 2 | a0001c0002t0001g0140 a0001c0002t0001g0141 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1070-1175G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177039 | |||||||
| chr7:139177041 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1070-1173G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177041 | |||||||
| chr7:139177171 | C | CA | 9 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1030dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177171 | ||||||
| chr7:139177171 | CA | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
93 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1070-1030delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177171 | ||||||
| chr7:139177277 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1070-937T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177277 | |||||||
| chr7:139177355 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
120 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1070-859A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177355 | |||||||
| chr7:139177482 | A | C | 1 | a0001c0001t0006g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1070-732A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177482 | |||||||
| chr7:139177499 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-715G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177499 | |||||||
| chr7:139177611 | A | AGTGT | 3 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0003t0015g0112 |
3 | HG02622.hp2 HG03139.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1070-586_1070-583d others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTGTGT | 11 | a0001c0001t0001g0063 a0001c0001t0001g0110 a0001c0001t0001g0114 others(8): Show |
11 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1070-588_1070-583d others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTGTGTG others(1): Show |
75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(72): Show |
95 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1070-590_1070-583d others(10): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTGTGTG others(3): Show |
30 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0064 others(27): Show |
32 | HG00140.hp2 HG01074.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1070-592_1070-583d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTGTGTG others(5): Show |
8 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(5): Show |
8 | HG02145.hp1 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-594_1070-583d others(14): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTGTGTG others(7): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0066 others(3): Show |
8 | HG01081.hp2 HG01123.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-596_1070-583d others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177611 | A | AGTTGTGT others(4): Show |
2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1070-601_1070-600i others(13): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | ||||||
| chr7:139177632 | A | G | 36 | a0001c0001t0002g0050 a0001c0001t0002g0054 a0001c0001t0002g0057 others(33): Show |
37 | HG02015.hp2 HG02071.hp1 HG02280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070-582A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177632 | |||||||
| chr7:139177634 | A | G | 8 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(5): Show |
8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-580A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177634 | |||||||
| chr7:139177656 | A | T | 1 | a0001c0001t0003g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1070-558A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177656 | |||||||
| chr7:139177686 | AAAATT | A | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.1070-524_1070-520d others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177686 | ||||||
| chr7:139177932 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1070-282C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177932 | |||||||
| chr7:139178011 | C | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0229 |
2 | NA18953.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1070-203C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139178011 | |||||||
| chr7:139178084 | A | G | 1 | a0001c0001t0017g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1070-130A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139178084 | |||||||
| chr7:139178682 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | NA18946.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1242+84G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178682 | |||||||
| chr7:139178720 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242+122C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178720 | |||||||
| chr7:139178771 | A | G | 1 | a0001c0002t0004g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1242+173A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178771 | |||||||
| chr7:139178774 | T | C | 1 | a0003c0006t0003g0265 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1242+176T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178774 | |||||||
| chr7:139178898 | TA | T | 8 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0002g0212 others(5): Show |
10 | HG00323.hp2 HG01361.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1242+312delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 139178898 | ||||||
| chr7:139178917 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1242+319T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178917 | |||||||
| chr7:139179105 | C | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1243-469C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179105 | |||||||
| chr7:139179112 | G | T | 1 | a0001c0001t0003g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243-462G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179112 | |||||||
| chr7:139179176 | G | C | 1 | a0002c0005t0001g0083 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1243-398G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179176 | |||||||
| chr7:139179465 | G | A | 2 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1243-109G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179465 | |||||||
| chr7:139179883 | C | G | 21 | a0001c0002t0004g0011 a0001c0002t0004g0028 a0001c0002t0004g0029 others(18): Show |
22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.1312+240C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139179883 | |||||||
| chr7:139179971 | C | T | 1 | a0001c0002t0002g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1312+328C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139179971 | |||||||
| chr7:139180065 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1312+422C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180065 | |||||||
| chr7:139180134 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1312+491G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180134 | |||||||
| chr7:139180162 | C | T | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+519C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180162 | |||||||
| chr7:139180221 | C | T | 1 | a0001c0001t0017g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312+578C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180221 | |||||||
| chr7:139180268 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0003g0026 |
3 | HG01074.hp1 NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1312+625C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180268 | |||||||
| chr7:139180362 | C | T | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312+719C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180362 | |||||||
| chr7:139180366 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1312+723G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180366 | |||||||
| chr7:139180446 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1313-646A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180446 | |||||||
| chr7:139180587 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(269): Show |
327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.1313-505A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180587 | |||||||
| chr7:139180664 | G | A | 1 | a0001c0001t0007g0204 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1313-428G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180664 | |||||||
| chr7:139180708 | C | CA | 67 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0002g0025 others(64): Show |
77 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1313-371dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139180708 | ||||||
| chr7:139180731 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1313-361T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180731 | |||||||
| chr7:139180737 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1313-355A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180737 | |||||||
| chr7:139180794 | C | T | 1 | a0001c0001t0003g0263 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1313-298C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180794 | |||||||
| chr7:139181659 | C | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0003g0240 others(1): Show |
6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+461C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139181659 | |||||||
| chr7:139182088 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1419+890G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182088 | |||||||
| chr7:139182106 | G | A | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1419+908G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182106 | |||||||
| chr7:139182161 | A | G | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1419+963A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182161 | |||||||
| chr7:139182179 | A | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0155 |
2 | HG01106.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1419+981A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182179 | |||||||
| chr7:139182187 | C | T | 3 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0002t0001g0142 |
3 | HG02622.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1419+989C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182187 | |||||||
| chr7:139182316 | C | CA | 9 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1419+1125dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139182316 | ||||||
| chr7:139182713 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1419+1515T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182713 | |||||||
| chr7:139183201 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+2003G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183201 | |||||||
| chr7:139183215 | GA | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(10): Show |
16 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1419+2019delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139183215 | ||||||
| chr7:139183311 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1419+2113G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183311 | |||||||
| chr7:139183325 | T | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0051 others(19): Show |
27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1419+2127T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183325 | |||||||
| chr7:139183330 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1419+2132C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183330 | |||||||
| chr7:139183346 | A | T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1419+2148A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183346 | |||||||
| chr7:139183517 | A | T | 1 | a0001c0001t0006g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1419+2319A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183517 | |||||||
| chr7:139183594 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1419+2396G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183594 | |||||||
| chr7:139183680 | A | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0051 others(19): Show |
27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1419+2482A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183680 | |||||||
| chr7:139183931 | A | C | 9 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1419+2733A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183931 | |||||||
| chr7:139184066 | G | A | 1 | a0001c0002t0004g0038 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1419+2868G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184066 | |||||||
| chr7:139184288 | T | A | 15 | a0001c0002t0004g0030 a0001c0002t0004g0031 a0001c0002t0004g0032 others(12): Show |
15 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.1419+3090T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184288 | |||||||
| chr7:139184340 | T | C | 7 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1420-3066T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184340 | |||||||
| chr7:139184501 | TTA | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0149 a0001c0001t0006g0153 |
3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-2903_1420-290 others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139184501 | ||||||
| chr7:139184506 | G | A | 3 | a0001c0001t0006g0148 a0001c0001t0006g0149 a0001c0001t0006g0153 |
3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-2900G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184506 | |||||||
| chr7:139184546 | G | A | 1 | a0001c0001t0018g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1420-2860G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184546 | |||||||
| chr7:139184589 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0157 a0001c0002t0004g0011 others(20): Show |
26 | HG00621.hp1 HG02015.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1420-2817A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184589 | |||||||
| chr7:139184636 | C | T | 5 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-2770C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184636 | |||||||
| chr7:139184637 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1420-2769G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184637 | |||||||
| chr7:139184776 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1420-2630C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184776 | |||||||
| chr7:139184780 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
109 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1420-2626C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184780 | |||||||
| chr7:139184792 | TGCCTGTA others(1366): Show |
T | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1420-2601_1420-122 others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139184792 | ||||||
| chr7:139184804 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2602C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184804 | |||||||
| chr7:139184819 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2587C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184819 | |||||||
| chr7:139184820 | T | C | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2586T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184820 | |||||||
| chr7:139184829 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2577C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184829 | |||||||
| chr7:139184836 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2570C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184836 | |||||||
| chr7:139184837 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2569A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184837 | |||||||
| chr7:139184850 | C | G | 6 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0003t0009g0108 others(3): Show |
6 | HG02280.hp2 HG02615.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-2556C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184850 | |||||||
| chr7:139184864 | T | C | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2542T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184864 | |||||||
| chr7:139184871 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2535A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184871 | |||||||
| chr7:139184993 | G | A | 2 | a0001c0001t0010g0151 a0001c0001t0010g0152 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1420-2413G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184993 | |||||||
| chr7:139185018 | C | T | 2 | a0001c0001t0003g0241 a0001c0001t0003g0242 |
2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1420-2388C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185018 | |||||||
| chr7:139185053 | C | CA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1420-2337dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185053 | ||||||
| chr7:139185053 | C | CAAA | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1420-2339_1420-233 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185053 | ||||||
| chr7:139185114 | T | C | 5 | a0001c0001t0003g0010 a0001c0001t0003g0260 a0001c0001t0003g0266 others(2): Show |
7 | HG00438.hp2 NA18961.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-2292T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185114 | |||||||
| chr7:139185201 | CAA | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(84): Show |
110 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1420-2197_1420-219 others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185201 | ||||||
| chr7:139185242 | T | C | 16 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(13): Show |
16 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1420-2164T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185242 | |||||||
| chr7:139185243 | G | A | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-2163G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185243 | |||||||
| chr7:139185298 | C | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2108C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185298 | |||||||
| chr7:139185406 | T | C | 1 | a0001c0001t0017g0169 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1420-2000T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185406 | |||||||
| chr7:139185878 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0018g0047 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1420-1528G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185878 | |||||||
| chr7:139186156 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0051 others(19): Show |
27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1420-1250G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186156 | |||||||
| chr7:139186361 | G | A | 2 | a0001c0001t0011g0143 a0001c0001t0011g0144 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1420-1045G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186361 | |||||||
| chr7:139186406 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1420-1000A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186406 | |||||||
| chr7:139186532 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1420-874C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186532 | |||||||
| chr7:139186656 | G | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0003g0240 others(1): Show |
6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-750G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186656 | |||||||
| chr7:139186676 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-730A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186676 | |||||||
| chr7:139186816 | C | T | 3 | a0001c0001t0006g0148 a0001c0001t0006g0149 a0001c0001t0006g0153 |
3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-590C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186816 | |||||||
| chr7:139186833 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1420-573G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186833 | |||||||
| chr7:139186860 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1420-546T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186860 | |||||||
| chr7:139186864 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1420-542A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186864 | |||||||
| chr7:139186890 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1420-516C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186890 | |||||||
| chr7:139186891 | G | A | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-515G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186891 | |||||||
| chr7:139186955 | G | A | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1420-451G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186955 | |||||||
| chr7:139186983 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-423A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186983 | |||||||
| chr7:139187064 | G | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-342G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187064 | |||||||
| chr7:139187075 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1420-331T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187075 | |||||||
| chr7:139187100 | C | CA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(127): Show |
152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1420-283dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | ||||||
| chr7:139187100 | C | CAA | 19 | a0001c0001t0001g0015 a0001c0001t0001g0060 a0001c0001t0001g0061 others(16): Show |
20 | HG00408.hp2 HG01891.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1420-284_1420-283d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | ||||||
| chr7:139187100 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1420-292_1420-283d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | ||||||
| chr7:139187192 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1420-214A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187192 | |||||||
| chr7:139187213 | A | C | 1 | a0001c0001t0005g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1420-193A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187213 | |||||||
| chr7:139187301 | C | T | 16 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0052 others(13): Show |
16 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1420-105C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187301 | |||||||
| chr7:139187321 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1420-85T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187321 | |||||||
| chr7:139187548 | A | G | 9 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+9A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187548 | |||||||
| chr7:139187599 | C | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(140): Show |
167 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1553+60C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187599 | |||||||
| chr7:139187922 | C | G | 1 | a0001c0002t0004g0041 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+383C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187922 | |||||||
| chr7:139188097 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1553+558C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188097 | |||||||
| chr7:139188098 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1553+559T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188098 | |||||||
| chr7:139188099 | T | G | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1553+560T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188099 | |||||||
| chr7:139188109 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
113 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1553+570T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188109 | |||||||
| chr7:139188141 | C | T | 7 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0053 others(4): Show |
7 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1553+602C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188141 | |||||||
| chr7:139188147 | C | G | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1553+608C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188147 | |||||||
| chr7:139188459 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1554-862C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188459 | |||||||
| chr7:139188900 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1554-421C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188900 | |||||||
| chr7:139189028 | G | T | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554-293G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139189028 | |||||||
| chr7:139189190 | A | G | 4 | a0001c0003t0009g0108 a0001c0003t0009g0109 a0001c0003t0009g0111 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554-131A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139189190 | |||||||
| chr7:139189255 | GTTTAT | G | 7 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1554-57_1554-53del others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139189255 |