Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 138255 |
| ensemblid | ENSG00000204711.9 |
| hgncid | 31422 |
| symbol | CFAP95 |
| name | cilia and flagella associated protein 95 |
| refseq_nuc | NM_001010940.3 |
| refseq_prot | NP_001010940.1 |
| ensembl_nuc | ENST00000377197.8 |
| ensembl_prot | ENSP00000366402.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 69820817 |
| end | 69906227 |
| strand | + |
| ver | v1.2 |
| region | chr9:69820817-69906227 |
| region5000 | chr9:69815817-69911227 |
| regionname0 | CFAP95_chr9_69820817_69906227 |
| regionname5000 | CFAP95_chr9_69815817_69911227 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 229 | 363 | 86 | 62 | 155 | 16 | 42 | 119 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0002 | 0/0 | 229 | 7 | 0 | 0 | 7 | 0 | 0 | 5 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0003 | 0/0 | 229 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0004 | 0/0 | 229 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0005 | 0/0 | 229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0006 | 0/0 | 229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0007 | 0/0 | 229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| a0008 | 0/0 | 229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | MDSLD others(224): Show |
chr9 | 69815817 | 69911227 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 687 | 283 | 75 | 47 | 118 | 10 | 31 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0001c0002 | 0/0 | 687 | 75 | 6 | 15 | 37 | 6 | 11 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0001c0005 | 0/0 | 687 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0001c0007 | 0/0 | 687 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0001c0013 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0002c0003 | 0/0 | 687 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0002c0008 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0003c0004 | 0/0 | 687 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0003c0012 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0004c0006 | 0/0 | 687 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0005c0010 | 0/0 | 687 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0006c0011 | 0/0 | 687 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0007c0009 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 | ||
| a0008c0014 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | ATGGA others(682): Show |
chr9 | 69815817 | 69911227 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 844 | 281 | 73 | 47 | 118 | 10 | 31 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0001t0002 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0001t0003 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0002t0001 | 0/0 | 844 | 74 | 6 | 15 | 36 | 6 | 11 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0002t0004 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0005t0001 | 0/0 | 844 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0007t0001 | 0/0 | 844 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0001c0013t0001 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0002c0003t0001 | 0/0 | 844 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0002c0008t0001 | 0/0 | 844 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0003c0004t0001 | 0/0 | 844 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0003c0012t0001 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0004c0006t0001 | 0/0 | 844 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0005c0010t0001 | 0/0 | 844 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0006c0011t0001 | 0/0 | 844 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0007c0009t0001 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| a0008c0014t0001 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | GTTCC others(839): Show |
chr9 | 69815817 | 69911227 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0001t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0007t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0001c0013t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0002c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0003c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0003c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0003c0012t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0004c0006t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0004c0006t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0005c0010t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0006c0011t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0007c0009t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| a0008c0014t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0333 | EUR | GBR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0353 | EUR | FIN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0267 | EUR | FIN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00639 | hp2 | a0005 | c0010 | t0001 | g0020 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00738 | hp2 | a0004 | c0006 | t0001 | g0085 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG00741 | hp2 | a0006 | c0011 | t0001 | g0256 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01070 | hp1 | a0004 | c0006 | t0001 | g0337 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0311 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0278 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0372 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0338 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0174 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0321 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0250 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | CDX | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02257 | hp2 | a0003 | c0004 | t0001 | g0089 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02258 | hp2 | a0003 | c0004 | t0001 | g0090 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0339 | AMR | PEL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0141 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0360 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02818 | hp1 | a0007 | c0009 | t0001 | g0324 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0370 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03225 | hp1 | a0001 | c0013 | t0001 | g0152 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03225 | hp2 | a0008 | c0014 | t0001 | g0173 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0348 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03516 | hp1 | a0003 | c0012 | t0001 | g0094 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03516 | hp2 | a0001 | c0007 | t0001 | g0154 | AFR | ESN | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0274 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0344 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0340 | SAS | PJL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0345 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0291 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18988 | hp1 | a0002 | c0008 | t0001 | g0176 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19000 | hp1 | a0002 | c0008 | t0001 | g0177 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | LWK | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | YRI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ASW | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0251 | EUR | TSI | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | GIH | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0235 | AFR | ACB | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | USA | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0120 | REF | REF | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0137 | REF | REF | CFAP95_chr9_69815817_69911227 | CFAP95 | chr9 | 69815817 | 69911227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69820916 | G | T | 1 | a0008 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.37G>T | p.Asp13Tyr | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/6 | 100/844 | 37/690 | 13/229 | chr9 | 69820916 | |||
| chr9:69820968 | A | C | 1 | a0002 | 7 | HG00673.hp1 HG02083.hp1 NA18979.hp1 others(4): Show |
missense_variant | MODERATE | c.89A>C | p.Lys30Thr | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/6 | 152/844 | 89/690 | 30/229 | chr9 | 69820968 | |||
| chr9:69844521 | C | T | 1 | a0003 | 4 | HG02257.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
missense_variant | MODERATE | c.157C>T | p.Arg53Cys | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/6 | 220/844 | 157/690 | 53/229 | chr9 | 69844521 | |||
| chr9:69856669 | G | A | 1 | a0007 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.376G>A | p.Glu126Lys | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/6 | 439/844 | 376/690 | 126/229 | chr9 | 69856669 | |||
| chr9:69886864 | A | G | 1 | a0006 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.476A>G | p.Asp159Gly | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/6 | 539/844 | 476/690 | 159/229 | chr9 | 69886864 | |||
| chr9:69886875 | C | T | 1 | a0005 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.487C>T | p.Pro163Ser | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/6 | 550/844 | 487/690 | 163/229 | chr9 | 69886875 | |||
| chr9:69906012 | C | T | 1 | a0004 | 2 | HG00738.hp2 HG01070.hp1 |
missense_variant | MODERATE | c.566C>T | p.Thr189Met | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 6/6 | 629/844 | 566/690 | 189/229 | chr9 | 69906012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69820972 | C | G | 1 | a0001c0013 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.93C>G | p.Gly31Gly | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/6 | 156/844 | 93/690 | 31/229 | chr9 | 69820972 | |||
| chr9:69856659 | C | T | 2 | a0001c0007 a0003c0012 |
3 | HG01884.hp1 HG03516.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.366C>T | p.Ser122Ser | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/6 | 429/844 | 366/690 | 122/229 | chr9 | 69856659 | |||
| chr9:69857915 | C | T | 4 | a0001c0002 a0002c0003 a0004c0006 others(1): Show |
83 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(80): Show |
synonymous_variant | LOW | c.387C>T | p.Thr129Thr | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/6 | 450/844 | 387/690 | 129/229 | chr9 | 69857915 | |||
| chr9:69906013 | G | A | 1 | a0001c0005 | 2 | HG02559.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.567G>A | p.Thr189Thr | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 6/6 | 630/844 | 567/690 | 189/229 | chr9 | 69906013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69820867 | C | G | 1 | a0001c0002t0004 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-13C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/6 | 13 | chr9 | 69820867 | ||||||
| chr9:69820876 | T | C | 1 | a0001c0001t0002 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/6 | 4 | chr9 | 69820876 | ||||||
| chr9:69906182 | T | A | 1 | a0001c0001t0003 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*46T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 6/6 | 46 | chr9 | 69906182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69821081 | A | G | 18 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+50A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821081 | |||||||
| chr9:69821308 | G | C | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+277G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821308 | |||||||
| chr9:69821432 | C | CA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
87 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.152+402dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69821432 | ||||||
| chr9:69821454 | G | C | 1 | a0004c0006t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.152+423G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821454 | |||||||
| chr9:69821533 | C | T | 2 | a0001c0001t0001g0353 a0001c0001t0001g0354 |
2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.152+502C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821533 | |||||||
| chr9:69821630 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.152+599G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821630 | |||||||
| chr9:69821741 | CT | C | 46 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0091 others(43): Show |
46 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.152+723delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69821741 | ||||||
| chr9:69821777 | T | G | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.152+746T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821777 | |||||||
| chr9:69821973 | G | T | 201 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.152+942G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69821973 | |||||||
| chr9:69822000 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+969C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822000 | |||||||
| chr9:69822085 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.152+1054T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822085 | |||||||
| chr9:69822102 | T | C | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+1071T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822102 | |||||||
| chr9:69822159 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152+1128T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822159 | |||||||
| chr9:69822182 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.152+1151A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822182 | |||||||
| chr9:69822199 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.152+1168A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822199 | |||||||
| chr9:69822271 | T | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+1240T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822271 | |||||||
| chr9:69822489 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152+1458C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822489 | |||||||
| chr9:69822585 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.152+1554C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822585 | |||||||
| chr9:69822776 | C | T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+1745C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822776 | |||||||
| chr9:69822906 | A | G | 6 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(3): Show |
6 | HG00544.hp2 NA18945.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+1875A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822906 | |||||||
| chr9:69822914 | G | T | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.152+1883G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69822914 | |||||||
| chr9:69823008 | A | G | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | HG00438.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.152+1977A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823008 | |||||||
| chr9:69823128 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.152+2097C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823128 | |||||||
| chr9:69823213 | G | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+2182G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823213 | |||||||
| chr9:69823257 | G | GAGA | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+2227_152+2228i others(5): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69823257 | ||||||
| chr9:69823316 | A | G | 84 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(81): Show |
85 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.152+2285A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823316 | |||||||
| chr9:69823374 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.152+2343C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823374 | |||||||
| chr9:69823584 | A | G | 3 | a0001c0001t0001g0088 a0003c0004t0001g0089 a0003c0004t0001g0090 |
3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.152+2553A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823584 | |||||||
| chr9:69823644 | C | T | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+2613C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823644 | |||||||
| chr9:69823846 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.152+2815C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823846 | |||||||
| chr9:69823967 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+2936C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823967 | |||||||
| chr9:69823969 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0005t0001g0159 |
3 | HG02572.hp1 HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.152+2938A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823969 | |||||||
| chr9:69823982 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.152+2951C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823982 | |||||||
| chr9:69823994 | C | T | 18 | a0001c0001t0001g0135 a0001c0001t0001g0356 a0001c0001t0001g0357 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+2963C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823994 | |||||||
| chr9:69823997 | C | G | 369 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.152+2966C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69823997 | |||||||
| chr9:69824008 | C | G | 98 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0133 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.152+2977C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824008 | |||||||
| chr9:69824009 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.152+2978T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824009 | |||||||
| chr9:69824021 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152+2990C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824021 | |||||||
| chr9:69824120 | C | A | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+3089C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824120 | |||||||
| chr9:69824167 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.152+3136G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824167 | |||||||
| chr9:69824269 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | NA18943.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152+3238A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824269 | |||||||
| chr9:69824368 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01255.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.152+3337A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824368 | |||||||
| chr9:69824424 | G | GC | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.152+3393_152+3394i others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824424 | |||||||
| chr9:69824455 | C | T | 83 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(80): Show |
84 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.152+3424C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824455 | |||||||
| chr9:69824493 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+3462C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824493 | |||||||
| chr9:69824558 | C | CT | 9 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0130 others(6): Show |
9 | HG01109.hp2 HG02074.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+3541dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69824558 | ||||||
| chr9:69824558 | CT | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0268 others(8): Show |
11 | HG00642.hp2 HG01175.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+3541delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69824558 | ||||||
| chr9:69824580 | G | A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0160 a0001c0001t0001g0161 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.152+3549G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824580 | |||||||
| chr9:69824598 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152+3567A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824598 | |||||||
| chr9:69824688 | A | T | 1 | a0001c0005t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+3657A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824688 | |||||||
| chr9:69824806 | A | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(96): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.152+3775A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69824806 | |||||||
| chr9:69825010 | G | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.152+3979G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825010 | |||||||
| chr9:69825117 | T | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4086T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825117 | |||||||
| chr9:69825136 | A | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4105A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825136 | |||||||
| chr9:69825304 | A | T | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.152+4273A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825304 | |||||||
| chr9:69825306 | C | A | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4275C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825306 | |||||||
| chr9:69825399 | G | A | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4368G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825399 | |||||||
| chr9:69825414 | C | T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4383C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825414 | |||||||
| chr9:69825424 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.152+4393T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825424 | |||||||
| chr9:69825535 | C | T | 201 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0074 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.152+4504C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825535 | |||||||
| chr9:69825742 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.152+4711C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825742 | |||||||
| chr9:69825824 | A | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+4793A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69825824 | |||||||
| chr9:69826034 | A | G | 18 | a0001c0001t0001g0249 a0001c0002t0001g0244 a0001c0002t0001g0246 others(15): Show |
18 | HG00280.hp2 HG00673.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+5003A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826034 | |||||||
| chr9:69826040 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.152+5009A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826040 | |||||||
| chr9:69826050 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.152+5019G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826050 | |||||||
| chr9:69826145 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152+5114T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826145 | |||||||
| chr9:69826180 | T | C | 1 | a0001c0002t0001g0011 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.152+5149T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826180 | |||||||
| chr9:69826195 | T | A | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.152+5164T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826195 | |||||||
| chr9:69826391 | C | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+5360C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826391 | |||||||
| chr9:69826475 | C | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.152+5444C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826475 | |||||||
| chr9:69826511 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.152+5480G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826511 | |||||||
| chr9:69826631 | A | G | 7 | a0001c0001t0001g0175 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG00741.hp1 HG01515.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+5600A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826631 | |||||||
| chr9:69826702 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152+5671G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826702 | |||||||
| chr9:69826706 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
89 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.152+5675G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826706 | |||||||
| chr9:69826896 | A | G | 1 | a0003c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152+5865A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69826896 | |||||||
| chr9:69827048 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+6017T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827048 | |||||||
| chr9:69827117 | T | C | 1 | a0003c0012t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.152+6086T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827117 | |||||||
| chr9:69827537 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+6506T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827537 | |||||||
| chr9:69827624 | C | T | 207 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(204): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.152+6593C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827624 | |||||||
| chr9:69827644 | C | T | 1 | a0001c0002t0001g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152+6613C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827644 | |||||||
| chr9:69827766 | G | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+6735G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827766 | |||||||
| chr9:69827802 | C | T | 1 | a0001c0007t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.152+6771C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827802 | |||||||
| chr9:69827821 | A | T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+6790A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69827821 | |||||||
| chr9:69828349 | A | G | 2 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.152+7318A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69828349 | |||||||
| chr9:69828926 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+7895T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69828926 | |||||||
| chr9:69828926 | T | C | 354 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(351): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.152+7895T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69828926 | |||||||
| chr9:69828944 | G | C | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+7913G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69828944 | |||||||
| chr9:69829037 | T | C | 263 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.152+8006T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829037 | |||||||
| chr9:69829104 | C | T | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+8073C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829104 | |||||||
| chr9:69829131 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+8100A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829131 | |||||||
| chr9:69829164 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152+8133C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829164 | |||||||
| chr9:69829180 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
88 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.152+8149C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829180 | |||||||
| chr9:69829308 | T | C | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+8277T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829308 | |||||||
| chr9:69829323 | A | C | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.152+8292A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829323 | |||||||
| chr9:69829475 | G | T | 88 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0266 others(85): Show |
89 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.152+8444G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829475 | |||||||
| chr9:69829597 | G | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+8566G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829597 | |||||||
| chr9:69829645 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+8614A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829645 | |||||||
| chr9:69829753 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.152+8722C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829753 | |||||||
| chr9:69829828 | C | G | 3 | a0001c0001t0001g0088 a0003c0004t0001g0089 a0003c0004t0001g0090 |
3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.152+8797C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829828 | |||||||
| chr9:69829932 | A | G | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+8901A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69829932 | |||||||
| chr9:69830172 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+9141T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830172 | |||||||
| chr9:69830247 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152+9216C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830247 | |||||||
| chr9:69830290 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152+9259C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830290 | |||||||
| chr9:69830300 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152+9269T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830300 | |||||||
| chr9:69830335 | C | T | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.152+9304C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830335 | |||||||
| chr9:69830362 | G | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+9331G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830362 | |||||||
| chr9:69830611 | G | T | 1 | a0001c0002t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152+9580G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830611 | |||||||
| chr9:69830772 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
89 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.152+9741C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830772 | |||||||
| chr9:69830788 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+9757T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830788 | |||||||
| chr9:69830897 | C | T | 1 | a0003c0012t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.152+9866C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69830897 | |||||||
| chr9:69831093 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+10062T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831093 | |||||||
| chr9:69831109 | T | C | 1 | a0001c0002t0001g0345 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.152+10078T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831109 | |||||||
| chr9:69831135 | T | C | 56 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.152+10104T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831135 | |||||||
| chr9:69831294 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+10263A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831294 | |||||||
| chr9:69831343 | T | C | 15 | a0001c0001t0001g0088 a0001c0001t0001g0160 a0001c0001t0001g0161 others(12): Show |
15 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+10312T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831343 | |||||||
| chr9:69831383 | A | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.152+10352A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831383 | |||||||
| chr9:69831408 | C | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0133 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.152+10377C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831408 | |||||||
| chr9:69831433 | C | CT | 84 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(81): Show |
85 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.152+10411dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69831433 | ||||||
| chr9:69831433 | CT | C | 24 | a0001c0001t0001g0133 a0001c0001t0001g0179 a0001c0001t0001g0180 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.152+10411delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69831433 | ||||||
| chr9:69831492 | C | G | 1 | a0001c0002t0001g0339 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.152+10461C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831492 | |||||||
| chr9:69831537 | T | A | 1 | a0001c0002t0001g0276 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.152+10506T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831537 | |||||||
| chr9:69831634 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+10603C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831634 | |||||||
| chr9:69831769 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.152+10738G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831769 | |||||||
| chr9:69831828 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+10797G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831828 | |||||||
| chr9:69831867 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | NA18612.hp2 NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.152+10836A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69831867 | |||||||
| chr9:69832045 | C | T | 2 | a0001c0002t0001g0068 a0001c0002t0001g0069 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.152+11014C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832045 | |||||||
| chr9:69832086 | T | G | 1 | a0001c0002t0001g0277 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.152+11055T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832086 | |||||||
| chr9:69832148 | C | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0338 a0004c0006t0001g0337 |
4 | HG01070.hp1 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+11117C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832148 | |||||||
| chr9:69832174 | A | C | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+11143A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832174 | |||||||
| chr9:69832191 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.152+11160C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832191 | |||||||
| chr9:69832273 | C | CA | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.152+11243dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832273 | ||||||
| chr9:69832287 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.152+11256T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832287 | |||||||
| chr9:69832416 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.152+11385G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832416 | |||||||
| chr9:69832418 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+11387G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832418 | |||||||
| chr9:69832601 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.152+11570A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832601 | |||||||
| chr9:69832610 | G | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+11579G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832610 | |||||||
| chr9:69832620 | A | AT | 10 | a0001c0001t0001g0359 a0001c0001t0001g0361 a0001c0001t0001g0362 others(7): Show |
10 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+11615dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTT | 87 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0098 others(84): Show |
88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.152+11613_152+1161 others(7): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTT | 39 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0110 others(36): Show |
39 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.152+11612_152+1161 others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0369 |
2 | HG02109.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.152+11606_152+1161 others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(4): Show |
30 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(27): Show |
30 | HG00544.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.152+11605_152+1161 others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(5): Show |
31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
37 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.152+11604_152+1161 others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0052 others(7): Show |
10 | HG00738.hp1 HG01255.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+11603_152+1161 others(17): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.152+11602_152+1161 others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0355 a0001c0002t0001g0069 |
3 | HG02080.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152+11601_152+1161 others(19): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0370 |
3 | HG00621.hp2 HG02922.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.152+11599_152+1161 others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01243.hp1 HG02027.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+11598_152+1161 others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0372 others(1): Show |
4 | HG01255.hp2 NA18970.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+11597_152+1161 others(23): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | AT | A | 37 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0136 others(34): Show |
37 | HG00597.hp1 HG00741.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.152+11615delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832620 | ATT | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0133 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.152+11614_152+1161 others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832620 | ||||||
| chr9:69832694 | C | CT | 96 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.152+11677dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832694 | ||||||
| chr9:69832694 | CT | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0170 a0001c0001t0001g0369 others(5): Show |
8 | HG01243.hp1 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+11677delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69832694 | ||||||
| chr9:69832739 | A | C | 369 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(366): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.152+11708A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832739 | |||||||
| chr9:69832742 | C | T | 17 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0001g0222 others(14): Show |
17 | HG01433.hp2 HG01934.hp2 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+11711C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832742 | |||||||
| chr9:69832802 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
87 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.153-11715G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832802 | |||||||
| chr9:69832901 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.153-11616T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69832901 | |||||||
| chr9:69833199 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.153-11318G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833199 | |||||||
| chr9:69833242 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153-11275T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833242 | |||||||
| chr9:69833333 | C | T | 1 | a0001c0001t0001g0368 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153-11184C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833333 | |||||||
| chr9:69833511 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.153-11006C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833511 | |||||||
| chr9:69833592 | C | T | 99 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(96): Show |
100 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.153-10925C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833592 | |||||||
| chr9:69833630 | C | T | 1 | a0001c0001t0001g0369 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-10887C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833630 | |||||||
| chr9:69833806 | A | G | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.153-10711A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833806 | |||||||
| chr9:69833821 | C | T | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-10696C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69833821 | |||||||
| chr9:69834042 | G | A | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.153-10475G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834042 | |||||||
| chr9:69834079 | C | T | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-10438C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834079 | |||||||
| chr9:69834235 | C | T | 1 | a0001c0002t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153-10282C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834235 | |||||||
| chr9:69834358 | G | A | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-10159G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834358 | |||||||
| chr9:69834399 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153-10118A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834399 | |||||||
| chr9:69834435 | AG | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-10081delG | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834435 | |||||||
| chr9:69834618 | T | A | 1 | a0001c0002t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153-9899T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834618 | |||||||
| chr9:69834720 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.153-9797A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834720 | |||||||
| chr9:69834820 | C | T | 98 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(95): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.153-9697C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834820 | |||||||
| chr9:69834828 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.153-9689A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834828 | |||||||
| chr9:69834846 | G | A | 1 | a0007c0009t0001g0324 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.153-9671G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834846 | |||||||
| chr9:69834885 | A | G | 5 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
5 | NA18941.hp1 NA18970.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-9632A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834885 | |||||||
| chr9:69834921 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.153-9596T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69834921 | |||||||
| chr9:69835191 | C | A | 44 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.153-9326C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835191 | |||||||
| chr9:69835282 | T | C | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-9235T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835282 | |||||||
| chr9:69835344 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-9173T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835344 | |||||||
| chr9:69835397 | G | A | 13 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(10): Show |
13 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-9120G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835397 | |||||||
| chr9:69835441 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.153-9076G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835441 | |||||||
| chr9:69835518 | G | T | 44 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.153-8999G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835518 | |||||||
| chr9:69835555 | T | C | 2 | a0001c0001t0001g0171 a0001c0002t0001g0172 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.153-8962T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835555 | |||||||
| chr9:69835563 | C | T | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.153-8954C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835563 | |||||||
| chr9:69835576 | C | T | 1 | a0001c0002t0001g0323 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.153-8941C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835576 | |||||||
| chr9:69835784 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-8733T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835784 | |||||||
| chr9:69835786 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.153-8731A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69835786 | |||||||
| chr9:69836111 | T | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0086 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.153-8406T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836111 | |||||||
| chr9:69836201 | C | T | 17 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-8316C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836201 | |||||||
| chr9:69836323 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.153-8194C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836323 | |||||||
| chr9:69836341 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.153-8176T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836341 | |||||||
| chr9:69836359 | A | G | 3 | a0001c0002t0001g0006 a0001c0002t0001g0338 a0004c0006t0001g0337 |
4 | HG01070.hp1 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-8158A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836359 | |||||||
| chr9:69836395 | C | T | 2 | a0001c0001t0001g0170 a0001c0007t0001g0174 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.153-8122C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836395 | |||||||
| chr9:69836437 | A | G | 1 | a0001c0002t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153-8080A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836437 | |||||||
| chr9:69836467 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | NA18943.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.153-8050C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836467 | |||||||
| chr9:69836600 | G | T | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.153-7917G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836600 | |||||||
| chr9:69836641 | A | G | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.153-7876A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836641 | |||||||
| chr9:69836672 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
86 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.153-7845C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836672 | |||||||
| chr9:69836689 | C | CT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.153-7812dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69836689 | ||||||
| chr9:69836689 | C | CTT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(10): Show |
14 | HG00438.hp1 HG01934.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-7813_153-7812d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69836689 | ||||||
| chr9:69836708 | A | G | 1 | a0001c0002t0001g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.153-7809A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836708 | |||||||
| chr9:69836743 | A | G | 85 | a0001c0001t0001g0171 a0001c0001t0001g0266 a0001c0001t0001g0268 others(82): Show |
86 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.153-7774A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836743 | |||||||
| chr9:69836837 | G | A | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.153-7680G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836837 | |||||||
| chr9:69836963 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.153-7554G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836963 | |||||||
| chr9:69836979 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.153-7538T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69836979 | |||||||
| chr9:69837011 | G | T | 13 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(10): Show |
13 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-7506G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837011 | |||||||
| chr9:69837133 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-7384T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837133 | |||||||
| chr9:69837263 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.153-7254G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837263 | |||||||
| chr9:69837387 | C | T | 1 | a0006c0011t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.153-7130C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837387 | |||||||
| chr9:69837427 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-7090C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837427 | |||||||
| chr9:69837439 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.153-7078G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837439 | |||||||
| chr9:69837536 | G | C | 12 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(9): Show |
12 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-6981G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837536 | |||||||
| chr9:69837677 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153-6840A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69837677 | |||||||
| chr9:69838013 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-6504C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838013 | |||||||
| chr9:69838051 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153-6466G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838051 | |||||||
| chr9:69838122 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0002g0134 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-6395T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838122 | |||||||
| chr9:69838127 | G | T | 1 | a0003c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153-6390G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838127 | |||||||
| chr9:69838208 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0265 a0003c0004t0001g0089 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-6309A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838208 | |||||||
| chr9:69838245 | T | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-6272T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838245 | |||||||
| chr9:69838339 | C | T | 81 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(78): Show |
82 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.153-6178C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838339 | |||||||
| chr9:69838340 | G | A | 40 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(37): Show |
40 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.153-6177G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838340 | |||||||
| chr9:69838546 | T | A | 2 | a0001c0001t0001g0140 a0001c0007t0001g0154 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.153-5971T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838546 | |||||||
| chr9:69838597 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
93 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.153-5920C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838597 | |||||||
| chr9:69838666 | T | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.153-5851T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838666 | |||||||
| chr9:69838669 | C | T | 1 | a0001c0002t0001g0339 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.153-5848C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838669 | |||||||
| chr9:69838801 | G | A | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-5716G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838801 | |||||||
| chr9:69838901 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18945.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.153-5616C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838901 | |||||||
| chr9:69838915 | C | T | 1 | a0001c0001t0001g0368 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153-5602C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69838915 | |||||||
| chr9:69838940 | GA | G | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.153-5574delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69838940 | ||||||
| chr9:69839048 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-5469G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839048 | |||||||
| chr9:69839140 | A | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.153-5377A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839140 | |||||||
| chr9:69839146 | T | C | 1 | a0001c0002t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153-5371T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839146 | |||||||
| chr9:69839217 | T | C | 1 | a0001c0002t0001g0326 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.153-5300T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839217 | |||||||
| chr9:69839461 | C | T | 3 | a0001c0001t0001g0088 a0003c0004t0001g0089 a0003c0004t0001g0090 |
3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.153-5056C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839461 | |||||||
| chr9:69839514 | C | T | 80 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(77): Show |
81 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.153-5003C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839514 | |||||||
| chr9:69839581 | C | T | 80 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0269 others(77): Show |
81 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.153-4936C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839581 | |||||||
| chr9:69839616 | C | T | 1 | a0001c0005t0001g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.153-4901C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839616 | |||||||
| chr9:69839716 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0002t0001g0172 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-4801A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839716 | |||||||
| chr9:69839753 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-4764A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839753 | |||||||
| chr9:69839840 | T | C | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.153-4677T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839840 | |||||||
| chr9:69839937 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.153-4580C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69839937 | |||||||
| chr9:69840076 | T | TA | 19 | a0001c0001t0001g0052 a0001c0001t0001g0110 a0001c0001t0001g0160 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.153-4426dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69840076 | ||||||
| chr9:69840076 | TA | T | 90 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0086 others(87): Show |
91 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.153-4426delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69840076 | ||||||
| chr9:69840096 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-4421G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840096 | |||||||
| chr9:69840278 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153-4239G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840278 | |||||||
| chr9:69840443 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153-4074A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840443 | |||||||
| chr9:69840612 | C | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0003c0004t0001g0141 |
3 | HG02451.hp1 HG03209.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.153-3905C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840612 | |||||||
| chr9:69840728 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.153-3789A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840728 | |||||||
| chr9:69840824 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.153-3693C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840824 | |||||||
| chr9:69840900 | C | T | 10 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(7): Show |
10 | HG02486.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-3617C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840900 | |||||||
| chr9:69840913 | G | T | 18 | a0001c0001t0001g0135 a0001c0001t0001g0356 a0001c0001t0001g0357 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.153-3604G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840913 | |||||||
| chr9:69840961 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-3556T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69840961 | |||||||
| chr9:69841124 | T | G | 1 | a0001c0002t0001g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-3393T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841124 | |||||||
| chr9:69841164 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0224 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.153-3353_153-3352i others(19): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841164 | |||||||
| chr9:69841164 | T | TTA | 5 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0164 others(2): Show |
5 | HG01074.hp2 HG01261.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3321_153-3320d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATA | 3 | a0001c0001t0001g0163 a0001c0002t0001g0279 a0001c0002t0001g0336 |
3 | HG01256.hp1 HG01993.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.153-3323_153-3320d others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATA | 14 | a0001c0001t0001g0133 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-3325_153-3320d others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(1): Show |
14 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
14 | HG00741.hp2 HG02083.hp1 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-3327_153-3320d others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(3): Show |
8 | a0001c0001t0001g0182 a0001c0001t0001g0249 a0001c0001t0001g0322 others(5): Show |
8 | HG00673.hp1 HG03041.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-3329_153-3320d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0195 others(3): Show |
6 | HG02056.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-3331_153-3320d others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(7): Show |
19 | a0001c0001t0001g0086 a0001c0001t0001g0211 a0001c0001t0001g0212 others(16): Show |
19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.153-3333_153-3320d others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(9): Show |
16 | a0001c0001t0001g0178 a0001c0001t0001g0218 a0001c0001t0001g0229 others(13): Show |
16 | HG00280.hp2 HG01496.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-3335_153-3320d others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(11): Show |
25 | a0001c0001t0001g0007 a0001c0001t0001g0175 a0001c0001t0001g0209 others(22): Show |
25 | HG00558.hp1 HG00621.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.153-3337_153-3320d others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(13): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0217 others(16): Show |
20 | HG00099.hp2 HG01070.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.153-3339_153-3320d others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(15): Show |
24 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0206 others(21): Show |
24 | HG01069.hp1 HG02300.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.153-3341_153-3320d others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(17): Show |
6 | a0001c0001t0001g0088 a0001c0001t0001g0205 a0001c0001t0001g0220 others(3): Show |
6 | HG00140.hp2 HG01891.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-3343_153-3320d others(26): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(19): Show |
7 | a0001c0001t0001g0201 a0001c0001t0001g0327 a0001c0001t0001g0350 others(4): Show |
7 | HG02647.hp2 HG03041.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-3345_153-3320d others(28): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(21): Show |
5 | a0001c0001t0001g0204 a0001c0002t0001g0006 a0001c0002t0001g0286 others(2): Show |
6 | HG01106.hp2 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-3347_153-3320d others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(23): Show |
6 | a0001c0001t0001g0203 a0001c0001t0001g0239 a0001c0001t0001g0349 others(3): Show |
6 | HG00438.hp2 HG01361.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-3349_153-3320d others(32): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0283 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.153-3320_153-3319i others(38): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTAATAT others(21): Show |
1 | a0001c0001t0001g0095 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.153-3352_153-3351i others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTATATA others(18): Show |
1 | a0001c0001t0001g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.153-3352_153-3351i others(27): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTATATA others(28): Show |
1 | a0001c0001t0001g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153-3352_153-3351i others(37): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTA | 4 | a0001c0001t0001g0013 a0001c0001t0001g0335 a0001c0001t0001g0371 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(3): Show |
1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153-3352_153-3351i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(9): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01943.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.153-3352_153-3351i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(11): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.153-3352_153-3351i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(13): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0125 others(1): Show |
4 | HG01106.hp1 HG01975.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(15): Show |
8 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0123 others(5): Show |
8 | HG01243.hp2 HG01256.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(17): Show |
10 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0110 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(26): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(19): Show |
7 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | HG00423.hp2 HG02004.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(28): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(21): Show |
4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0268 others(1): Show |
4 | HG01099.hp2 HG01978.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(23): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0114 a0001c0001t0001g0315 others(1): Show |
4 | HG00642.hp2 HG02258.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3352_153-3351i others(32): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(25): Show |
2 | a0001c0001t0001g0131 a0001c0001t0001g0314 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.153-3352_153-3351i others(34): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(27): Show |
2 | a0001c0001t0001g0098 a0001c0001t0001g0113 |
2 | HG03942.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.153-3352_153-3351i others(36): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | T | TTTTATAT others(29): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01358.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.153-3352_153-3351i others(38): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTA | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0138 others(16): Show |
19 | HG00140.hp1 HG01099.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.153-3321_153-3320d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATA | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0036 others(11): Show |
14 | HG00738.hp2 HG01074.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-3323_153-3320d others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATATA | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
82 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.153-3325_153-3320d others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00099.hp1 HG00642.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3329_153-3320d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATATAT others(5): Show |
T | 2 | a0001c0001t0001g0367 a0001c0002t0001g0251 |
2 | HG03486.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.153-3331_153-3320d others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3335_153-3320d others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841164 | TTATATAT others(13): Show |
T | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.153-3339_153-3320d others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841164 | ||||||
| chr9:69841168 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0370 others(1): Show |
4 | HG01099.hp1 HG01255.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3349A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841168 | |||||||
| chr9:69841170 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0036 others(2): Show |
5 | HG01361.hp2 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3347A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841170 | |||||||
| chr9:69841172 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
82 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.153-3345A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841172 | |||||||
| chr9:69841189 | T | TATATATA others(11): Show |
1 | a0001c0002t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.153-3320_153-3319i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69841189 | ||||||
| chr9:69841192 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.153-3325A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841192 | |||||||
| chr9:69841197 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0263 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.153-3320_153-3319i others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841197 | |||||||
| chr9:69841197 | T | TATATATA others(14): Show |
2 | a0001c0001t0001g0225 a0007c0009t0001g0324 |
2 | HG02818.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.153-3320_153-3319i others(23): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841197 | |||||||
| chr9:69841342 | G | T | 1 | a0001c0002t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.153-3175G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841342 | |||||||
| chr9:69841387 | G | T | 41 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.153-3130G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841387 | |||||||
| chr9:69841575 | G | A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0133 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.153-2942G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841575 | |||||||
| chr9:69841611 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-2906C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69841611 | |||||||
| chr9:69842130 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-2387G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842130 | |||||||
| chr9:69842132 | G | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0133 others(92): Show |
96 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.153-2385G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842132 | |||||||
| chr9:69842297 | G | C | 3 | a0001c0001t0001g0088 a0003c0004t0001g0089 a0003c0004t0001g0090 |
3 | HG01891.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.153-2220G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842297 | |||||||
| chr9:69842313 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153-2204G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842313 | |||||||
| chr9:69842345 | G | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0322 |
2 | NA18955.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.153-2172G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842345 | |||||||
| chr9:69842452 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.153-2065A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842452 | |||||||
| chr9:69842572 | TA | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0213 others(1): Show |
4 | HG01069.hp2 HG01167.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-1938delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69842572 | ||||||
| chr9:69842860 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.153-1657C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842860 | |||||||
| chr9:69842861 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-1656G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842861 | |||||||
| chr9:69842864 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.153-1653C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842864 | |||||||
| chr9:69842866 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.153-1651A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842866 | |||||||
| chr9:69842867 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.153-1650C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842867 | |||||||
| chr9:69842954 | G | T | 74 | a0001c0001t0001g0171 a0001c0001t0001g0219 a0001c0001t0001g0268 others(71): Show |
75 | HG00140.hp1 HG00558.hp1 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.153-1563G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69842954 | |||||||
| chr9:69843248 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153-1269A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843248 | |||||||
| chr9:69843261 | T | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0369 a0001c0001t0001g0370 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-1256T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843261 | |||||||
| chr9:69843443 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0149 a0001c0001t0001g0170 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-1074C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843443 | |||||||
| chr9:69843451 | T | TC | 7 | a0001c0001t0001g0061 a0001c0001t0001g0114 a0001c0001t0001g0127 others(4): Show |
7 | HG00621.hp2 HG02109.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-1061dupC | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843451 | ||||||
| chr9:69843491 | T | TCCTCCTC others(8): Show |
1 | a0001c0002t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.153-1024_153-1010d others(17): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843491 | ||||||
| chr9:69843491 | T | TCCTCCTC others(23): Show |
1 | a0001c0001t0001g0019 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.153-1001_153-1000i others(32): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843491 | ||||||
| chr9:69843494 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.153-1023T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843494 | |||||||
| chr9:69843494 | T | TCCTCCTC others(7): Show |
1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153-1010_153-1009i others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843494 | ||||||
| chr9:69843500 | T | TCCCCCCC others(10): Show |
1 | a0001c0001t0001g0036 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.153-1010_153-1009i others(19): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843500 | ||||||
| chr9:69843500 | TC | T | 22 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0304 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.153-1010delC | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843500 | ||||||
| chr9:69843502 | C | CCCTCCTC others(8): Show |
1 | a0001c0001t0001g0342 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.153-1013_153-1012i others(17): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843502 | ||||||
| chr9:69843502 | C | CTCCTCCT others(3): Show |
1 | a0001c0001t0001g0266 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.153-1015_153-1014i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843502 | |||||||
| chr9:69843503 | C | CCCCCCTC others(20): Show |
1 | a0001c0002t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.153-1010_153-1009i others(29): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843503 | ||||||
| chr9:69843503 | CCCCCTCC others(13): Show |
C | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-1011_153-992de others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843503 | ||||||
| chr9:69843504 | CCCCTCCT others(3): Show |
C | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.153-1010_153-1001d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843504 | ||||||
| chr9:69843505 | C | CCCCCCCC others(19): Show |
1 | a0001c0001t0001g0314 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153-1010_153-1009i others(28): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | CCCCCCCT others(9): Show |
1 | a0001c0001t0001g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.153-1010_153-1009i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | CCCCCCCT others(12): Show |
1 | a0001c0002t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153-1010_153-1009i others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | CCCCTCCT others(18): Show |
1 | a0002c0003t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.153-1010_153-1009i others(27): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | CCCTCCTC others(5): Show |
2 | a0001c0002t0001g0295 a0001c0002t0001g0308 |
2 | HG01069.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.153-969_153-958dup others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | CCCTCCTC others(8): Show |
4 | a0001c0001t0001g0219 a0001c0002t0001g0303 a0001c0002t0001g0306 others(1): Show |
4 | HG01169.hp1 HG02293.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-972_153-958dup others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | C | T | 33 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0096 others(30): Show |
33 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.153-1012C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843505 | |||||||
| chr9:69843505 | CCCTCCTC others(5): Show |
C | 2 | a0001c0001t0001g0242 a0003c0012t0001g0094 |
2 | HG03516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.153-969_153-958del others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | CCCTCCTC others(8): Show |
C | 2 | a0001c0001t0001g0243 a0004c0006t0001g0085 |
2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.153-972_153-958del others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | CCCTCCTC others(17): Show |
C | 1 | a0003c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153-981_153-958del others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843505 | CCCTCCTC others(26): Show |
C | 1 | a0001c0007t0001g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.153-990_153-958del others(33): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843505 | ||||||
| chr9:69843506 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0221 |
3 | HG00140.hp2 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.153-1011C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843506 | |||||||
| chr9:69843506 | CCT | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
13 | HG01358.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-1009_153-1008d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843506 | CCTCCTCC others(4): Show |
C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0187 a0001c0001t0001g0231 others(2): Show |
5 | HG00280.hp1 HG00423.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-1009_153-999de others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843506 | CCTCCTCC others(7): Show |
C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0002t0001g0234 others(3): Show |
6 | HG03579.hp2 NA18941.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1009_153-996de others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843506 | CCTCCTCC others(10): Show |
C | 1 | a0001c0001t0001g0249 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153-1009_153-993de others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843506 | CCTCCTCC others(13): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.153-1009_153-990de others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843506 | CCTCCTCC others(16): Show |
C | 1 | a0001c0002t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.153-1009_153-987de others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843506 | ||||||
| chr9:69843507 | CT | C | 7 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0001g0230 others(4): Show |
7 | HG02056.hp2 HG02109.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-1009delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843507 | |||||||
| chr9:69843507 | CTCCT | C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0194 others(1): Show |
4 | HG02886.hp2 HG03654.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-1009_153-1006d others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843507 | |||||||
| chr9:69843507 | CTCCTCCT others(3): Show |
C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0180 a0001c0001t0001g0185 others(5): Show |
8 | HG00544.hp1 HG03669.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-1009_153-1000d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843507 | |||||||
| chr9:69843507 | CTCCTCCT others(6): Show |
C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0261 a0001c0002t0001g0252 others(3): Show |
6 | HG00280.hp2 HG00673.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1009_153-997de others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843507 | |||||||
| chr9:69843507 | CTCCTCCT others(12): Show |
C | 1 | a0002c0003t0001g0255 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.153-1009_153-991de others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843507 | |||||||
| chr9:69843508 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0153 others(18): Show |
21 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.153-1009T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843508 | |||||||
| chr9:69843508 | T | C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0149 a0001c0001t0001g0204 others(4): Show |
7 | HG01106.hp2 HG01256.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-1009T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843508 | |||||||
| chr9:69843508 | T | TCCTCCTC others(5): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0028 |
2 | HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843508 | ||||||
| chr9:69843511 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0230 |
2 | HG02055.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.153-1006T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843511 | |||||||
| chr9:69843511 | T | TCCTCCCC others(2): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
12 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-1001_153-1000i others(11): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843511 | ||||||
| chr9:69843511 | T | TCCTCCCC others(3): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0072 |
3 | HG02258.hp1 HG03669.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843511 | ||||||
| chr9:69843511 | T | TCCTCCCC others(4): Show |
1 | a0001c0001t0001g0023 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(13): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843511 | ||||||
| chr9:69843511 | T | TCCTCCCC others(17): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0064 |
2 | HG01993.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(26): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843511 | ||||||
| chr9:69843511 | T | TCCTCCCC others(16): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG02165.hp1 NA18945.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(25): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843511 | ||||||
| chr9:69843514 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0160 a0001c0001t0002g0134 others(2): Show |
5 | HG02055.hp2 HG02074.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-1003T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843514 | |||||||
| chr9:69843514 | T | TCCCCCCC others(3): Show |
1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-1001_153-1000i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(11): Show |
1 | a0001c0001t0001g0063 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(14): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0005c0010t0001g0020 |
3 | HG00639.hp2 HG01255.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(23): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(13): Show |
1 | a0001c0001t0001g0067 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(15): Show |
1 | a0001c0001t0001g0033 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.153-1001_153-1000i others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(9): Show |
1 | a0001c0001t0001g0021 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.153-1001_153-1000i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(12): Show |
1 | a0001c0002t0001g0011 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(13): Show |
1 | a0001c0001t0001g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(22): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(15): Show |
1 | a0001c0001t0001g0058 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.153-1001_153-1000i others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843514 | T | TCCCCCCC others(26): Show |
2 | a0001c0001t0001g0040 a0001c0002t0001g0041 |
2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.153-1001_153-1000i others(35): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843514 | ||||||
| chr9:69843517 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(26): Show |
32 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.153-1000T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843517 | |||||||
| chr9:69843520 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(18): Show |
24 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.153-997T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843520 | |||||||
| chr9:69843520 | T | TCCCCC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(3): Show |
7 | HG00544.hp2 HG01975.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-995_153-994ins others(5): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843520 | ||||||
| chr9:69843523 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0170 others(2): Show |
5 | HG01884.hp1 HG02040.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-994T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843523 | |||||||
| chr9:69843523 | T | TCC | 6 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0054 others(3): Show |
6 | HG00597.hp2 HG01261.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-993_153-992dup others(2): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843523 | ||||||
| chr9:69843523 | T | TCCCCC | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(5): Show |
9 | HG00673.hp2 HG01943.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-992_153-991ins others(5): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843523 | ||||||
| chr9:69843526 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0031 others(9): Show |
12 | HG00597.hp2 HG01261.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-991T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843526 | |||||||
| chr9:69843526 | T | TCCTCCCC others(1): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0050 others(3): Show |
6 | HG00621.hp2 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-986_153-985ins others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843526 | ||||||
| chr9:69843526 | T | TCCTCCTC others(4): Show |
1 | a0001c0001t0001g0055 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.153-983_153-982ins others(11): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843526 | ||||||
| chr9:69843528 | CT | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0084 |
3 | HG01175.hp2 HG04199.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.153-988delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843528 | |||||||
| chr9:69843529 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0042 others(1): Show |
4 | HG03927.hp1 NA18995.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-988T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843529 | |||||||
| chr9:69843529 | T | TCC | 4 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0077 others(1): Show |
4 | HG02523.hp2 NA18612.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-987_153-986dup others(2): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843529 | ||||||
| chr9:69843530 | CCTCCTCC others(35): Show |
C | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153-984_153-943del others(42): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843530 | ||||||
| chr9:69843531 | CT | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 |
4 | HG00438.hp1 HG02080.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-985delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843531 | |||||||
| chr9:69843532 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0032 others(6): Show |
10 | HG01175.hp2 HG02523.hp2 HG04199.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-985T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843532 | |||||||
| chr9:69843533 | CCTCCTCC others(23): Show |
C | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.153-981_153-952del others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843533 | ||||||
| chr9:69843533 | CCTCCTCC others(26): Show |
C | 1 | a0001c0002t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.153-981_153-949del others(33): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843533 | ||||||
| chr9:69843535 | T | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(2): Show |
6 | HG00438.hp1 HG02080.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-982T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843535 | |||||||
| chr9:69843538 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.153-979T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843538 | |||||||
| chr9:69843540 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-977C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843540 | |||||||
| chr9:69843541 | TCCTCCTC others(7): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.153-975_153-962del others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843541 | |||||||
| chr9:69843541 | TCCTCCTC others(13): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153-975_153-956del others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843541 | |||||||
| chr9:69843542 | CCTCCTCC others(14): Show |
C | 2 | a0001c0001t0001g0354 a0002c0003t0001g0245 |
2 | HG00733.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.153-972_153-952del others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843542 | ||||||
| chr9:69843542 | CCTCCTCC others(26): Show |
C | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.153-972_153-940del others(33): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843542 | ||||||
| chr9:69843542 | CCTCCTCC others(41): Show |
C | 2 | a0001c0001t0001g0304 a0001c0013t0001g0152 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.153-972_153-925del others(48): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843542 | ||||||
| chr9:69843542 | CCTCCTCC others(44): Show |
C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0153 |
3 | HG01884.hp2 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.153-972_153-922del others(51): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843542 | ||||||
| chr9:69843543 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-974C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843543 | |||||||
| chr9:69843545 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0001g0198 |
3 | NA19004.hp1 NA19060.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.153-972C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843545 | |||||||
| chr9:69843545 | CCTCCTCC others(14): Show |
C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0189 a0001c0001t0001g0216 others(2): Show |
5 | HG01261.hp1 HG02056.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-969_153-949del others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843545 | ||||||
| chr9:69843545 | CCTCCTCC others(17): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153-969_153-946del others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843545 | ||||||
| chr9:69843545 | CCTCCTCC others(20): Show |
C | 2 | a0001c0001t0001g0220 a0001c0002t0001g0260 |
2 | HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.153-969_153-943del others(27): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843545 | ||||||
| chr9:69843545 | CCTCCTCC others(26): Show |
C | 1 | a0001c0001t0001g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.153-969_153-937del others(33): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843545 | ||||||
| chr9:69843546 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-971C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843546 | |||||||
| chr9:69843547 | TCCTCCTC others(1): Show |
T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0310 |
3 | HG00639.hp1 HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.153-969_153-962del others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843547 | |||||||
| chr9:69843548 | C | CCTTTCTC others(5): Show |
1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.153-967_153-966ins others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843548 | ||||||
| chr9:69843548 | C | T | 11 | a0001c0001t0001g0140 a0001c0001t0001g0161 a0001c0001t0001g0168 others(8): Show |
11 | HG00741.hp1 HG01069.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-969C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843548 | |||||||
| chr9:69843548 | CCTCCTCC others(5): Show |
C | 1 | a0001c0001t0001g0228 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.153-966_153-955del others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843548 | ||||||
| chr9:69843548 | CCTCCTCC others(14): Show |
C | 1 | a0001c0002t0001g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-966_153-946del others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843548 | ||||||
| chr9:69843550 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.153-967T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843550 | |||||||
| chr9:69843550 | TCC | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0160 a0001c0001t0001g0169 |
3 | HG01358.hp1 HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.153-966_153-965del others(2): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843550 | |||||||
| chr9:69843551 | C | T | 18 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0001g0161 others(15): Show |
18 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-966C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843551 | |||||||
| chr9:69843551 | CCTCCTCC others(38): Show |
C | 2 | a0001c0001t0001g0361 a0001c0001t0001g0362 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153-963_153-919del others(45): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843551 | ||||||
| chr9:69843551 | CCTCCTCC others(41): Show |
C | 4 | a0001c0001t0001g0356 a0001c0001t0001g0359 a0001c0001t0001g0363 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-963_153-916del others(48): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843551 | ||||||
| chr9:69843551 | CCTCCTCC others(44): Show |
C | 1 | a0001c0001t0001g0367 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.153-963_153-913del others(51): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843551 | ||||||
| chr9:69843554 | C | CCTTCTT | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0320 |
3 | NA18945.hp1 NA18992.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.153-961_153-960ins others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | C | T | 36 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0001g0139 others(33): Show |
36 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.153-963C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843554 | |||||||
| chr9:69843554 | CCTCCTTC others(5): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0224 |
2 | NA18941.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.153-960_153-949del others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(8): Show |
C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0207 a0001c0001t0001g0221 others(2): Show |
5 | HG00140.hp2 HG01433.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-960_153-946del others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(11): Show |
C | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.153-960_153-943del others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(14): Show |
C | 1 | a0001c0001t0001g0229 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.153-960_153-940del others(21): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(23): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-960_153-931del others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(32): Show |
C | 1 | a0001c0001t0001g0372 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.153-960_153-922del others(39): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(38): Show |
C | 3 | a0001c0001t0001g0355 a0001c0001t0001g0364 a0001c0001t0001g0365 |
3 | HG03453.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.153-960_153-916del others(45): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843554 | CCTCCTTC others(41): Show |
C | 3 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0366 |
3 | HG02818.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.153-960_153-913del others(48): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843554 | ||||||
| chr9:69843556 | TC | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0131 a0001c0001t0001g0160 others(2): Show |
5 | HG00099.hp1 HG01358.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-959delC | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843556 | ||||||
| chr9:69843557 | C | CCTCCTCC others(17): Show |
1 | a0001c0001t0001g0330 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.153-958_153-957ins others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | C | CCTCCTTC others(8): Show |
1 | a0001c0001t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.153-958_153-957ins others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | C | CCTT | 4 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0132 others(1): Show |
4 | HG00558.hp2 HG01243.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-889_153-887dup others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | C | CCTTCTT | 4 | a0001c0001t0001g0107 a0001c0001t0001g0143 a0001c0001t0001g0266 others(1): Show |
4 | HG01943.hp2 HG04204.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-892_153-887dup others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | C | CCTTCTTC others(8): Show |
1 | a0001c0001t0001g0296 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.153-901_153-887dup others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | C | T | 59 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0091 others(56): Show |
59 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.153-960C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843557 | |||||||
| chr9:69843557 | CCTT | C | 10 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0270 others(7): Show |
10 | HG02040.hp2 HG02572.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-889_153-887del others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(23): Show |
27 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.153-892_153-887del others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(2): Show |
C | 11 | a0001c0001t0001g0099 a0001c0001t0001g0210 a0001c0001t0001g0227 others(8): Show |
11 | HG00280.hp1 HG00438.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-895_153-887del others(9): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(5): Show |
C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0263 a0001c0002t0001g0215 others(1): Show |
4 | HG01496.hp1 HG02698.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-898_153-887del others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(8): Show |
C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0171 a0001c0001t0001g0181 others(5): Show |
8 | HG01256.hp1 HG01358.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-901_153-887del others(15): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(11): Show |
C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0001t0001g0203 others(1): Show |
5 | HG00099.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-904_153-887del others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(17): Show |
C | 2 | a0001c0001t0001g0117 a0001c0002t0001g0321 |
2 | HG01934.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.153-910_153-887del others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(20): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.153-913_153-887del others(27): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(23): Show |
C | 1 | a0001c0001t0001g0369 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-916_153-887del others(30): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(29): Show |
C | 1 | a0001c0001t0001g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.153-922_153-887del others(36): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(32): Show |
C | 1 | a0001c0001t0001g0368 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153-925_153-887del others(39): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843557 | CCTTCTTC others(35): Show |
C | 1 | a0001c0001t0001g0371 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153-928_153-887del others(42): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843557 | ||||||
| chr9:69843558 | CT | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0127 others(2): Show |
5 | HG00639.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-957delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843558 | ||||||
| chr9:69843559 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0126 |
2 | HG01106.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.153-958T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843559 | |||||||
| chr9:69843559 | T | TCCTCCTC others(4): Show |
1 | a0001c0002t0001g0288 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.153-958_153-957ins others(11): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843559 | |||||||
| chr9:69843560 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
153 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.153-957T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843560 | |||||||
| chr9:69843562 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0002t0001g0011 others(2): Show |
5 | HG01975.hp1 NA18959.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-955T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843562 | |||||||
| chr9:69843563 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
148 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.153-954T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843563 | |||||||
| chr9:69843565 | T | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0288 a0001c0002t0001g0332 |
3 | NA18959.hp2 NA19010.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.153-952T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843565 | |||||||
| chr9:69843566 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
158 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.153-951T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843566 | |||||||
| chr9:69843568 | T | C | 5 | a0001c0001t0001g0354 a0001c0002t0001g0011 a0001c0002t0001g0288 others(2): Show |
5 | HG00733.hp1 HG03516.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-949T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843568 | |||||||
| chr9:69843569 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
161 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.153-948T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843569 | |||||||
| chr9:69843571 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0353 a0001c0002t0001g0011 others(2): Show |
5 | HG00280.hp1 HG01261.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-946T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843571 | |||||||
| chr9:69843572 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
161 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.153-945T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843572 | |||||||
| chr9:69843574 | T | C | 4 | a0001c0001t0001g0165 a0001c0002t0001g0011 a0001c0002t0001g0288 others(1): Show |
4 | HG02145.hp2 NA18959.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-943T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843574 | |||||||
| chr9:69843575 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
164 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.153-942T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843575 | |||||||
| chr9:69843577 | T | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0288 a0001c0002t0001g0332 |
3 | NA18959.hp2 NA19010.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.153-940T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843577 | |||||||
| chr9:69843578 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
162 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.153-939T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843578 | |||||||
| chr9:69843580 | T | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0288 a0001c0002t0001g0332 |
3 | NA18959.hp2 NA19010.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.153-937T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843580 | |||||||
| chr9:69843581 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.153-936T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843581 | |||||||
| chr9:69843583 | T | C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0288 a0001c0002t0001g0332 |
3 | NA18959.hp2 NA19010.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.153-934T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843583 | |||||||
| chr9:69843584 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
149 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.153-933T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843584 | |||||||
| chr9:69843586 | T | C | 2 | a0001c0002t0001g0288 a0001c0002t0001g0332 |
2 | NA18959.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.153-931T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843586 | |||||||
| chr9:69843587 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
126 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.153-930T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843587 | |||||||
| chr9:69843589 | T | C | 1 | a0001c0002t0001g0332 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.153-928T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843589 | |||||||
| chr9:69843590 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): Show |
87 | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.153-927T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843590 | |||||||
| chr9:69843592 | T | C | 1 | a0001c0002t0001g0332 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.153-925T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843592 | |||||||
| chr9:69843593 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(21): Show |
25 | HG00438.hp1 HG00544.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.153-924T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843593 | |||||||
| chr9:69843596 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0170 others(3): Show |
7 | HG00438.hp1 HG01256.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-921T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843596 | |||||||
| chr9:69843599 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0002t0001g0279 |
4 | HG00438.hp1 HG01256.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-918T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843599 | |||||||
| chr9:69843602 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0010 |
3 | HG00438.hp1 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.153-915T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843602 | |||||||
| chr9:69843607 | TTCTTCTT others(17): Show |
T | 1 | a0001c0002t0001g0049 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.153-907_153-884del others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843607 | ||||||
| chr9:69843616 | T | G | 52 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0133 others(49): Show |
52 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.153-901T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843616 | |||||||
| chr9:69843616 | T | TTCTTCTT others(5): Show |
1 | a0001c0001t0001g0198 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.153-890_153-889ins others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843616 | ||||||
| chr9:69843619 | T | G | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.153-898T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843619 | |||||||
| chr9:69843628 | TTCC | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
205 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.153-875_153-873del others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843628 | ||||||
| chr9:69843628 | TTCCTCC | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0005c0010t0001g0020 |
3 | HG00639.hp2 HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.153-878_153-873del others(6): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 69843628 | ||||||
| chr9:69843631 | C | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0153 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-886C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843631 | |||||||
| chr9:69843632 | T | C | 3 | a0001c0001t0001g0170 a0001c0007t0001g0174 a0008c0014t0001g0173 |
3 | HG01884.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.153-885T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843632 | |||||||
| chr9:69843636 | C | A | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.153-881C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843636 | |||||||
| chr9:69843915 | C | T | 3 | a0001c0001t0001g0170 a0001c0007t0001g0174 a0008c0014t0001g0173 |
3 | HG01884.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.153-602C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843915 | |||||||
| chr9:69843967 | G | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
119 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.153-550G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69843967 | |||||||
| chr9:69844198 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153-319T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69844198 | |||||||
| chr9:69844263 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.153-254G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69844263 | |||||||
| chr9:69844274 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
184 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.153-243G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69844274 | |||||||
| chr9:69844384 | T | C | 3 | a0001c0001t0001g0170 a0001c0007t0001g0174 a0008c0014t0001g0173 |
3 | HG01884.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.153-133T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69844384 | |||||||
| chr9:69844437 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.153-80T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 1/5 | chr9 | 69844437 | |||||||
| chr9:69844651 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
120 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.261+26G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69844651 | |||||||
| chr9:69844724 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
87 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.261+99G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69844724 | |||||||
| chr9:69844783 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261+158T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69844783 | |||||||
| chr9:69845054 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.261+429G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845054 | |||||||
| chr9:69845135 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.261+510T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845135 | |||||||
| chr9:69845181 | C | G | 2 | a0001c0001t0001g0140 a0001c0007t0001g0154 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.261+556C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845181 | |||||||
| chr9:69845203 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.261+578A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845203 | |||||||
| chr9:69845511 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+886C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845511 | |||||||
| chr9:69845552 | T | A | 3 | a0003c0004t0001g0089 a0003c0004t0001g0090 a0003c0004t0001g0141 |
3 | HG02257.hp2 HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.261+927T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845552 | |||||||
| chr9:69845692 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
222 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.261+1067A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845692 | |||||||
| chr9:69845716 | AAC | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0133 a0001c0001t0001g0179 others(56): Show |
59 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.261+1095_261+1096d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 69845716 | ||||||
| chr9:69845745 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.261+1120C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845745 | |||||||
| chr9:69845748 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.261+1123C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845748 | |||||||
| chr9:69845995 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0133 a0001c0001t0001g0179 others(56): Show |
59 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.261+1370A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69845995 | |||||||
| chr9:69846087 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.261+1462T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69846087 | |||||||
| chr9:69846390 | T | C | 60 | a0001c0001t0001g0052 a0001c0001t0001g0133 a0001c0001t0001g0179 others(57): Show |
60 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.261+1765T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69846390 | |||||||
| chr9:69846739 | A | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0355 a0001c0001t0001g0356 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.261+2114A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69846739 | |||||||
| chr9:69846798 | G | T | 3 | a0001c0001t0001g0170 a0001c0007t0001g0174 a0008c0014t0001g0173 |
3 | HG01884.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.261+2173G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69846798 | |||||||
| chr9:69846986 | A | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0163 |
2 | HG01993.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.261+2361A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69846986 | |||||||
| chr9:69847070 | G | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.261+2445G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847070 | |||||||
| chr9:69847143 | T | C | 23 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0001g0111 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.261+2518T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847143 | |||||||
| chr9:69847254 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.261+2629C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847254 | |||||||
| chr9:69847394 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.261+2769A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847394 | |||||||
| chr9:69847617 | G | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0149 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+2992G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847617 | |||||||
| chr9:69847797 | T | C | 1 | a0006c0011t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.261+3172T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847797 | |||||||
| chr9:69847943 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0105 |
2 | NA18964.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.261+3318C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847943 | |||||||
| chr9:69847973 | A | T | 36 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(33): Show |
36 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.261+3348A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69847973 | |||||||
| chr9:69848006 | C | T | 1 | a0001c0005t0001g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.261+3381C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69848006 | |||||||
| chr9:69848105 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.261+3480C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69848105 | |||||||
| chr9:69848451 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | HG01884.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+3826A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69848451 | |||||||
| chr9:69848553 | G | A | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.261+3928G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69848553 | |||||||
| chr9:69848939 | T | G | 1 | a0001c0001t0001g0342 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.261+4314T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69848939 | |||||||
| chr9:69849158 | A | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
221 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.261+4533A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849158 | |||||||
| chr9:69849182 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.261+4557C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849182 | |||||||
| chr9:69849203 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
161 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.261+4578G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849203 | |||||||
| chr9:69849277 | G | A | 1 | a0001c0002t0001g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.261+4652G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849277 | |||||||
| chr9:69849331 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0066 |
2 | NA18975.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.261+4706G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849331 | |||||||
| chr9:69849475 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0236 |
2 | NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.261+4850G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849475 | |||||||
| chr9:69849497 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.261+4872G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849497 | |||||||
| chr9:69849554 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.261+4929G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849554 | |||||||
| chr9:69849879 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0135 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.261+5254G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849879 | |||||||
| chr9:69849990 | A | T | 1 | a0001c0007t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.261+5365A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69849990 | |||||||
| chr9:69850025 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG03486.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.261+5400C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850025 | |||||||
| chr9:69850047 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0005t0001g0159 |
3 | HG02572.hp1 HG02896.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.261+5422A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850047 | |||||||
| chr9:69850164 | G | A | 1 | a0002c0003t0001g0248 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.261+5539G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850164 | |||||||
| chr9:69850613 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.262-5942A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850613 | |||||||
| chr9:69850698 | T | C | 1 | a0003c0012t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.262-5857T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850698 | |||||||
| chr9:69850757 | A | G | 36 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(33): Show |
36 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.262-5798A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850757 | |||||||
| chr9:69850780 | T | C | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-5775T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850780 | |||||||
| chr9:69850781 | C | T | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-5774C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850781 | |||||||
| chr9:69850859 | T | C | 1 | a0001c0002t0001g0286 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.262-5696T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850859 | |||||||
| chr9:69850901 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0214 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.262-5654G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69850901 | |||||||
| chr9:69851070 | A | G | 1 | a0002c0003t0001g0245 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.262-5485A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851070 | |||||||
| chr9:69851097 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-5458T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851097 | |||||||
| chr9:69851141 | A | T | 1 | a0001c0001t0001g0372 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.262-5414A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851141 | |||||||
| chr9:69851217 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.262-5338G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851217 | |||||||
| chr9:69851339 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.262-5216T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851339 | |||||||
| chr9:69851359 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
153 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.262-5196A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851359 | |||||||
| chr9:69851508 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-5047C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851508 | |||||||
| chr9:69851510 | A | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0029 others(3): Show |
7 | HG00639.hp2 HG00673.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-5045A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851510 | |||||||
| chr9:69851510 | A | G | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(360): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.262-5045A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851510 | |||||||
| chr9:69851575 | C | A | 1 | a0001c0005t0001g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262-4980C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851575 | |||||||
| chr9:69851686 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.262-4869A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851686 | |||||||
| chr9:69851717 | C | T | 22 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0135 others(19): Show |
22 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-4838C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851717 | |||||||
| chr9:69851876 | G | GA | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
217 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.262-4667dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 69851876 | ||||||
| chr9:69851981 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
88 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.262-4574C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69851981 | |||||||
| chr9:69852164 | TA | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0146 others(39): Show |
43 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.262-4390delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852164 | |||||||
| chr9:69852166 | T | TA | 3 | a0001c0001t0001g0007 a0001c0002t0001g0274 a0001c0002t0001g0278 |
3 | HG01167.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.262-4389_262-4388i others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852166 | |||||||
| chr9:69852167 | T | A | 24 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0139 others(21): Show |
24 | HG01243.hp1 HG01255.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.262-4388T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852167 | |||||||
| chr9:69852169 | T | A | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0371 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-4386T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852169 | |||||||
| chr9:69852307 | T | C | 1 | a0003c0012t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.262-4248T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852307 | |||||||
| chr9:69852414 | T | A | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-4141T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852414 | |||||||
| chr9:69852415 | G | T | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-4140G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852415 | |||||||
| chr9:69852498 | C | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0029 others(3): Show |
7 | HG00639.hp2 HG00673.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-4057C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852498 | |||||||
| chr9:69852679 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.262-3876C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852679 | |||||||
| chr9:69852957 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0073 |
3 | HG00673.hp2 NA18967.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.262-3598C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852957 | |||||||
| chr9:69852989 | A | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-3566A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69852989 | |||||||
| chr9:69853006 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0151 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.262-3549A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853006 | |||||||
| chr9:69853049 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
11 | HG00597.hp2 HG02132.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.262-3506C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853049 | |||||||
| chr9:69853188 | C | G | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.262-3367C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853188 | |||||||
| chr9:69853260 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.262-3295A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853260 | |||||||
| chr9:69853294 | C | A | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-3261C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853294 | |||||||
| chr9:69853295 | T | C | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-3260T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853295 | |||||||
| chr9:69853297 | C | T | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262-3258C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853297 | |||||||
| chr9:69853470 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.262-3085T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853470 | |||||||
| chr9:69853783 | T | G | 1 | a0001c0002t0001g0326 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.262-2772T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853783 | |||||||
| chr9:69853793 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262-2762G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69853793 | |||||||
| chr9:69854118 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0151 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.262-2437C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854118 | |||||||
| chr9:69854119 | G | A | 4 | a0001c0001t0001g0369 a0001c0001t0001g0370 a0001c0001t0001g0371 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-2436G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854119 | |||||||
| chr9:69854124 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.262-2431T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854124 | |||||||
| chr9:69854356 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-2199C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854356 | |||||||
| chr9:69854429 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-2126G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854429 | |||||||
| chr9:69854453 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-2102G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854453 | |||||||
| chr9:69854846 | G | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0135 a0001c0001t0001g0151 others(18): Show |
21 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-1709G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854846 | |||||||
| chr9:69854927 | A | T | 60 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0052 others(57): Show |
60 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.262-1628A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69854927 | |||||||
| chr9:69855022 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.262-1533A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855022 | |||||||
| chr9:69855235 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.262-1320T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855235 | |||||||
| chr9:69855257 | T | C | 1 | a0001c0002t0001g0252 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.262-1298T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855257 | |||||||
| chr9:69855373 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.262-1182A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855373 | |||||||
| chr9:69855400 | A | G | 19 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0171 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.262-1155A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855400 | |||||||
| chr9:69855402 | C | T | 8 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0239 others(5): Show |
8 | HG00741.hp1 HG01515.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-1153C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855402 | |||||||
| chr9:69855427 | C | G | 1 | a0001c0001t0001g0371 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.262-1128C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855427 | |||||||
| chr9:69855491 | C | T | 7 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-1064C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855491 | |||||||
| chr9:69855531 | G | A | 1 | a0001c0005t0001g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262-1024G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855531 | |||||||
| chr9:69855545 | G | A | 6 | a0001c0002t0001g0035 a0001c0002t0001g0274 a0001c0002t0001g0278 others(3): Show |
6 | HG01167.hp1 HG01256.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-1010G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855545 | |||||||
| chr9:69855561 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.262-994C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855561 | |||||||
| chr9:69855578 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0203 a0001c0001t0001g0233 others(1): Show |
5 | HG00099.hp2 HG01358.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-977G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855578 | |||||||
| chr9:69855633 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.262-922G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855633 | |||||||
| chr9:69855661 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.262-894G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855661 | |||||||
| chr9:69855858 | G | C | 1 | a0003c0004t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262-697G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69855858 | |||||||
| chr9:69856151 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0155 a0001c0007t0001g0174 |
3 | HG01099.hp1 HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.262-404C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69856151 | |||||||
| chr9:69856236 | G | T | 1 | a0003c0012t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.262-319G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69856236 | |||||||
| chr9:69856377 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.262-178A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69856377 | |||||||
| chr9:69856425 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0114 |
3 | NA18940.hp1 NA18954.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.262-130A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 2/5 | chr9 | 69856425 | |||||||
| chr9:69856830 | C | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0091 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.380+157C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856830 | |||||||
| chr9:69856850 | G | A | 1 | a0001c0001t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380+177G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856850 | |||||||
| chr9:69856888 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.380+215C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856888 | |||||||
| chr9:69856916 | A | G | 1 | a0001c0002t0001g0281 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.380+243A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856916 | |||||||
| chr9:69856920 | G | GT | 65 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0078 others(62): Show |
65 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.380+265dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69856920 | ||||||
| chr9:69856920 | G | GTT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
175 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.380+264_380+265dup others(2): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69856920 | ||||||
| chr9:69856920 | G | GTTT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0039 others(11): Show |
14 | HG00621.hp2 HG01175.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+263_380+265dup others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69856920 | ||||||
| chr9:69856920 | GT | G | 27 | a0001c0001t0001g0087 a0001c0001t0001g0135 a0001c0001t0001g0140 others(24): Show |
27 | HG01243.hp1 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.380+265delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69856920 | ||||||
| chr9:69856946 | A | T | 6 | a0001c0002t0001g0022 a0001c0002t0001g0285 a0001c0002t0001g0293 others(3): Show |
6 | HG01069.hp1 HG01261.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+273A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856946 | |||||||
| chr9:69856976 | G | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0040 |
4 | NA18944.hp2 NA18960.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+303G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856976 | |||||||
| chr9:69856991 | G | A | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+318G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69856991 | |||||||
| chr9:69857115 | A | G | 1 | a0001c0002t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.380+442A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857115 | |||||||
| chr9:69857136 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.380+463A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857136 | |||||||
| chr9:69857150 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.380+477C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857150 | |||||||
| chr9:69857174 | T | C | 12 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0265 others(9): Show |
12 | HG01496.hp2 HG01884.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.380+501T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857174 | |||||||
| chr9:69857175 | G | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+502G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857175 | |||||||
| chr9:69857332 | C | A | 1 | a0001c0001t0001g0371 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.381-577C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857332 | |||||||
| chr9:69857368 | C | CTGT | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | NA18747.hp1 NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.381-540_381-538dup others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69857368 | ||||||
| chr9:69857585 | C | T | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.381-324C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857585 | |||||||
| chr9:69857586 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.381-323G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857586 | |||||||
| chr9:69857616 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.381-293T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857616 | |||||||
| chr9:69857650 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381-259G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857650 | |||||||
| chr9:69857661 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-248G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857661 | |||||||
| chr9:69857686 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.381-223G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857686 | |||||||
| chr9:69857759 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.381-150C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857759 | |||||||
| chr9:69857760 | G | T | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.381-149G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857760 | |||||||
| chr9:69857827 | C | T | 8 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0239 others(5): Show |
8 | HG00741.hp1 HG01515.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.381-82C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857827 | |||||||
| chr9:69857830 | TA | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
255 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.381-76delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 69857830 | ||||||
| chr9:69857831 | A | T | 1 | a0001c0002t0001g0281 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.381-78A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857831 | |||||||
| chr9:69857855 | A | T | 1 | a0001c0002t0001g0281 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.381-54A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 3/5 | chr9 | 69857855 | |||||||
| chr9:69858137 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
276 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.449+160T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858137 | |||||||
| chr9:69858138 | G | A | 146 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0088 others(143): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.449+161G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858138 | |||||||
| chr9:69858145 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.449+168A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858145 | |||||||
| chr9:69858155 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.449+178G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858155 | |||||||
| chr9:69858256 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.449+279G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858256 | |||||||
| chr9:69858267 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.449+290A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858267 | |||||||
| chr9:69858331 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0151 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.449+354A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858331 | |||||||
| chr9:69858501 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
276 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.449+524T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858501 | |||||||
| chr9:69858617 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.449+640T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858617 | |||||||
| chr9:69858708 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0151 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.449+731C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858708 | |||||||
| chr9:69858721 | A | G | 2 | a0001c0001t0001g0349 a0001c0001t0001g0350 |
2 | HG00438.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.449+744A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69858721 | |||||||
| chr9:69859080 | C | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.449+1103C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859080 | |||||||
| chr9:69859297 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.449+1320C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859297 | |||||||
| chr9:69859370 | T | G | 1 | a0001c0002t0001g0345 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.449+1393T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859370 | |||||||
| chr9:69859469 | C | G | 1 | a0002c0003t0001g0245 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.449+1492C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859469 | |||||||
| chr9:69859730 | G | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+1753G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859730 | |||||||
| chr9:69859923 | A | G | 3 | a0001c0007t0001g0154 a0001c0007t0001g0174 a0003c0012t0001g0094 |
3 | HG01884.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.449+1946A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859923 | |||||||
| chr9:69859982 | G | A | 1 | a0002c0003t0001g0255 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.449+2005G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859982 | |||||||
| chr9:69859990 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0203 a0001c0001t0001g0233 others(1): Show |
5 | HG00099.hp2 HG01358.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+2013C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69859990 | |||||||
| chr9:69860094 | G | A | 14 | a0001c0002t0001g0035 a0001c0002t0001g0208 a0001c0002t0001g0274 others(11): Show |
14 | HG01167.hp1 HG01256.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.449+2117G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860094 | |||||||
| chr9:69860276 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0304 a0001c0013t0001g0152 |
3 | HG02922.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449+2299C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860276 | |||||||
| chr9:69860409 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.449+2432G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860409 | |||||||
| chr9:69860543 | G | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+2566G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860543 | |||||||
| chr9:69860573 | C | T | 1 | a0001c0002t0001g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.449+2596C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860573 | |||||||
| chr9:69860604 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0210 |
2 | NA18965.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.449+2627C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860604 | |||||||
| chr9:69860604 | CT | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.449+2642delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69860604 | ||||||
| chr9:69860604 | CTT | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0140 others(11): Show |
14 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.449+2641_449+2642d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69860604 | ||||||
| chr9:69860632 | CT | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+2659delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69860632 | ||||||
| chr9:69860657 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.449+2680G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860657 | |||||||
| chr9:69860803 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0341 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.449+2826C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69860803 | |||||||
| chr9:69861016 | G | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(5): Show |
8 | HG01070.hp1 HG01496.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+3039G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861016 | |||||||
| chr9:69861022 | C | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
312 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.449+3045C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861022 | |||||||
| chr9:69861099 | C | T | 27 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(24): Show |
27 | HG00609.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.449+3122C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861099 | |||||||
| chr9:69861150 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
77 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.449+3173C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861150 | |||||||
| chr9:69861192 | G | A | 10 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.449+3215G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861192 | |||||||
| chr9:69861547 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.449+3570C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861547 | |||||||
| chr9:69861595 | C | G | 1 | a0001c0001t0001g0363 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.449+3618C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861595 | |||||||
| chr9:69861597 | C | G | 1 | a0001c0002t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.449+3620C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861597 | |||||||
| chr9:69861706 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.449+3729C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861706 | |||||||
| chr9:69861730 | C | CA | 49 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0026 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.449+3776dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861730 | ||||||
| chr9:69861730 | C | CAA | 12 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0131 others(9): Show |
12 | HG01074.hp2 HG01978.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.449+3775_449+3776d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861730 | ||||||
| chr9:69861730 | CA | C | 107 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0039 others(104): Show |
108 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.449+3776delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861730 | ||||||
| chr9:69861730 | CAA | C | 28 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0054 others(25): Show |
28 | HG00597.hp1 HG00733.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.449+3775_449+3776d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861730 | ||||||
| chr9:69861730 | CAAA | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0185 a0001c0001t0001g0216 others(4): Show |
7 | HG01496.hp1 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.449+3774_449+3776d others(5): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861730 | ||||||
| chr9:69861742 | A | C | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.449+3765A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861742 | |||||||
| chr9:69861749 | A | AC | 15 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0219 others(12): Show |
15 | HG01255.hp2 HG02451.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.449+3772_449+3773i others(3): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861749 | |||||||
| chr9:69861749 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
75 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.449+3772A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861749 | |||||||
| chr9:69861753 | A | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG01516.hp2 HG01517.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.449+3776A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861753 | |||||||
| chr9:69861753 | A | G | 1 | a0001c0001t0001g0365 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.449+3776A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861753 | |||||||
| chr9:69861761 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
311 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.449+3784T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861761 | |||||||
| chr9:69861852 | CAG | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
257 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.449+3879_449+3880d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69861852 | ||||||
| chr9:69861853 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+3876A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861853 | |||||||
| chr9:69861855 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
257 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.449+3878A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69861855 | |||||||
| chr9:69862033 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0356 a0001c0001t0001g0361 others(1): Show |
4 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+4056C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862033 | |||||||
| chr9:69862096 | A | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG00140.hp2 HG01106.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.449+4119A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862096 | |||||||
| chr9:69862203 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+4226T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862203 | |||||||
| chr9:69862390 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+4413C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862390 | |||||||
| chr9:69862512 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0218 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+4535A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862512 | |||||||
| chr9:69862597 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+4620G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862597 | |||||||
| chr9:69862695 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.449+4718G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862695 | |||||||
| chr9:69862771 | C | T | 33 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(30): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.449+4794C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862771 | |||||||
| chr9:69862864 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.449+4887A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862864 | |||||||
| chr9:69862996 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
273 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.449+5019A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69862996 | |||||||
| chr9:69863113 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449+5136G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863113 | |||||||
| chr9:69863184 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.449+5207A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863184 | |||||||
| chr9:69863277 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.449+5300G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863277 | |||||||
| chr9:69863674 | C | T | 3 | a0001c0002t0001g0280 a0001c0002t0001g0299 a0001c0002t0001g0329 |
3 | HG02040.hp2 NA18966.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.449+5697C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863674 | |||||||
| chr9:69863726 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0031 others(3): Show |
9 | HG00597.hp2 HG03927.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.449+5749G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863726 | |||||||
| chr9:69863751 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.449+5774T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863751 | |||||||
| chr9:69863776 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0171 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.449+5799T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863776 | |||||||
| chr9:69863851 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+5874C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863851 | |||||||
| chr9:69863852 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.449+5875G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863852 | |||||||
| chr9:69863888 | A | C | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.449+5911A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863888 | |||||||
| chr9:69863921 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
254 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.449+5944T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69863921 | |||||||
| chr9:69864024 | G | C | 14 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(11): Show |
14 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.449+6047G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864024 | |||||||
| chr9:69864084 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.449+6107C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864084 | |||||||
| chr9:69864130 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.449+6153G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864130 | |||||||
| chr9:69864256 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.449+6279A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864256 | |||||||
| chr9:69864393 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.449+6416G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864393 | |||||||
| chr9:69864440 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
310 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.449+6463T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864440 | |||||||
| chr9:69864495 | G | C | 2 | a0001c0007t0001g0154 a0001c0007t0001g0174 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.449+6518G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864495 | |||||||
| chr9:69864668 | G | T | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+6691G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864668 | |||||||
| chr9:69864675 | T | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.449+6698T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864675 | |||||||
| chr9:69864747 | T | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
276 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.449+6770T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864747 | |||||||
| chr9:69864828 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
92 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.449+6851C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69864828 | |||||||
| chr9:69865073 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
272 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.449+7096A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865073 | |||||||
| chr9:69865123 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.449+7146A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865123 | |||||||
| chr9:69865524 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
254 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.449+7547G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865524 | |||||||
| chr9:69865551 | C | T | 2 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.449+7574C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865551 | |||||||
| chr9:69865562 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+7585G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865562 | |||||||
| chr9:69865754 | A | G | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.449+7777A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865754 | |||||||
| chr9:69865755 | G | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+7778G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865755 | |||||||
| chr9:69865845 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.449+7868A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69865845 | |||||||
| chr9:69866137 | A | T | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+8160A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866137 | |||||||
| chr9:69866395 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.449+8418G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866395 | |||||||
| chr9:69866550 | G | A | 81 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0022 others(78): Show |
82 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.449+8573G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866550 | |||||||
| chr9:69866585 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.449+8608A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866585 | |||||||
| chr9:69866631 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.449+8654G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866631 | |||||||
| chr9:69866831 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+8854G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866831 | |||||||
| chr9:69866862 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+8885G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866862 | |||||||
| chr9:69866892 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+8915G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866892 | |||||||
| chr9:69866996 | G | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+9019G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866996 | |||||||
| chr9:69866997 | C | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+9020C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866997 | |||||||
| chr9:69866998 | G | A | 1 | a0001c0007t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.449+9021G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69866998 | |||||||
| chr9:69867111 | T | C | 2 | a0001c0001t0001g0327 a0007c0009t0001g0324 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.449+9134T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867111 | |||||||
| chr9:69867119 | G | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+9142G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867119 | |||||||
| chr9:69867164 | G | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
254 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.449+9187G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867164 | |||||||
| chr9:69867191 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG01261.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.449+9214C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867191 | |||||||
| chr9:69867315 | C | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+9338C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867315 | |||||||
| chr9:69867597 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449+9620A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867597 | |||||||
| chr9:69867683 | A | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | NA18989.hp1 NA18998.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.449+9706A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867683 | |||||||
| chr9:69867835 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+9858T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867835 | |||||||
| chr9:69867926 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
271 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.449+9949G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69867926 | |||||||
| chr9:69868114 | C | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
275 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.449+10137C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868114 | |||||||
| chr9:69868185 | A | G | 38 | a0001c0001t0001g0086 a0001c0001t0001g0097 a0001c0001t0001g0116 others(35): Show |
38 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.449+10208A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868185 | |||||||
| chr9:69868275 | A | AT | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
253 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.449+10305dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69868275 | ||||||
| chr9:69868346 | C | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.449+10369C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868346 | |||||||
| chr9:69868350 | C | CA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
275 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.449+10381dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69868350 | ||||||
| chr9:69868427 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
253 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.449+10450G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868427 | |||||||
| chr9:69868482 | A | G | 5 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
5 | NA18941.hp1 NA18970.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+10505A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868482 | |||||||
| chr9:69868552 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+10575G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868552 | |||||||
| chr9:69868571 | T | C | 1 | a0001c0002t0001g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.449+10594T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868571 | |||||||
| chr9:69868598 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.449+10621C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868598 | |||||||
| chr9:69868662 | C | CA | 38 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0030 others(35): Show |
38 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.449+10700dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69868662 | ||||||
| chr9:69868662 | CA | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
231 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.449+10700delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69868662 | ||||||
| chr9:69868684 | A | C | 42 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(39): Show |
42 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.449+10707A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868684 | |||||||
| chr9:69868731 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
75 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.449+10754A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868731 | |||||||
| chr9:69868805 | GA | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
107 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.449+10841delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69868805 | ||||||
| chr9:69868809 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.449+10832A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868809 | |||||||
| chr9:69868870 | T | C | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+10893T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868870 | |||||||
| chr9:69868897 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0218 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.449+10920G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868897 | |||||||
| chr9:69868919 | CA | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+10943delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868919 | |||||||
| chr9:69868989 | C | T | 1 | a0001c0007t0001g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.449+11012C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69868989 | |||||||
| chr9:69869001 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.449+11024G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869001 | |||||||
| chr9:69869022 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
309 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.449+11045C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869022 | |||||||
| chr9:69869386 | G | A | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.449+11409G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869386 | |||||||
| chr9:69869515 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
75 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.449+11538G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869515 | |||||||
| chr9:69869551 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.449+11574G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869551 | |||||||
| chr9:69869611 | G | T | 1 | a0003c0004t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449+11634G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869611 | |||||||
| chr9:69869691 | C | T | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+11714C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869691 | |||||||
| chr9:69869709 | G | A | 2 | a0002c0008t0001g0176 a0002c0008t0001g0177 |
2 | NA18988.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.449+11732G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869709 | |||||||
| chr9:69869742 | T | TA | 368 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(365): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.449+11774dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69869742 | ||||||
| chr9:69869781 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
92 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.449+11804A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69869781 | |||||||
| chr9:69870076 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+12099T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870076 | |||||||
| chr9:69870182 | TA | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+12207delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69870182 | ||||||
| chr9:69870258 | A | G | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+12281A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870258 | |||||||
| chr9:69870334 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0171 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.449+12357T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870334 | |||||||
| chr9:69870459 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(4): Show |
8 | HG00438.hp1 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+12482C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870459 | |||||||
| chr9:69870509 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.449+12532T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870509 | |||||||
| chr9:69870524 | C | T | 1 | a0001c0001t0001g0361 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.449+12547C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870524 | |||||||
| chr9:69870545 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.449+12568A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870545 | |||||||
| chr9:69870581 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+12604C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870581 | |||||||
| chr9:69870707 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.449+12730G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870707 | |||||||
| chr9:69870775 | G | A | 1 | a0001c0002t0001g0323 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.449+12798G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870775 | |||||||
| chr9:69870820 | T | C | 2 | a0001c0002t0001g0103 a0001c0002t0001g0251 |
2 | HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.449+12843T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69870820 | |||||||
| chr9:69871016 | C | T | 1 | a0001c0001t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.449+13039C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871016 | |||||||
| chr9:69871132 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(19): Show |
22 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.449+13155C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871132 | |||||||
| chr9:69871270 | T | C | 1 | a0001c0002t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.449+13293T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871270 | |||||||
| chr9:69871291 | C | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(15): Show |
18 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+13314C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871291 | |||||||
| chr9:69871297 | A | G | 2 | a0001c0007t0001g0154 a0001c0007t0001g0174 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.449+13320A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871297 | |||||||
| chr9:69871419 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.449+13442G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871419 | |||||||
| chr9:69871557 | G | A | 1 | a0001c0002t0001g0253 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.449+13580G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871557 | |||||||
| chr9:69871574 | T | TA | 7 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0218 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+13611dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69871574 | ||||||
| chr9:69871584 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0171 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.449+13607A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871584 | |||||||
| chr9:69871624 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.449+13647C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871624 | |||||||
| chr9:69871640 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.449+13663T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871640 | |||||||
| chr9:69871988 | C | T | 118 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0088 others(115): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.449+14011C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69871988 | |||||||
| chr9:69872017 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+14040T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872017 | |||||||
| chr9:69872281 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.449+14304G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872281 | |||||||
| chr9:69872351 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.449+14374A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872351 | |||||||
| chr9:69872362 | A | C | 1 | a0001c0002t0001g0299 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.449+14385A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872362 | |||||||
| chr9:69872436 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-14402T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872436 | |||||||
| chr9:69872678 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.450-14160T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872678 | |||||||
| chr9:69872732 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-14106C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872732 | |||||||
| chr9:69872787 | C | G | 1 | a0001c0002t0001g0295 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.450-14051C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872787 | |||||||
| chr9:69872852 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.450-13986A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69872852 | |||||||
| chr9:69873066 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(14): Show |
17 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.450-13772G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873066 | |||||||
| chr9:69873099 | C | T | 1 | a0001c0002t0001g0281 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.450-13739C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873099 | |||||||
| chr9:69873129 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450-13709C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873129 | |||||||
| chr9:69873223 | A | T | 1 | a0001c0001t0001g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.450-13615A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873223 | |||||||
| chr9:69873232 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.450-13606A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873232 | |||||||
| chr9:69873261 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.450-13577T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873261 | |||||||
| chr9:69873285 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.450-13553C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873285 | |||||||
| chr9:69873312 | T | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-13526T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873312 | |||||||
| chr9:69873323 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.450-13515T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873323 | |||||||
| chr9:69873414 | TTTTG | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-13400_450-1339 others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69873414 | ||||||
| chr9:69873501 | C | T | 29 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0091 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.450-13337C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873501 | |||||||
| chr9:69873502 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0319 |
2 | HG01496.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.450-13336G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873502 | |||||||
| chr9:69873522 | C | T | 1 | a0003c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450-13316C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873522 | |||||||
| chr9:69873526 | G | A | 26 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(23): Show |
26 | HG00609.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.450-13312G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873526 | |||||||
| chr9:69873555 | C | T | 24 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0091 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.450-13283C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873555 | |||||||
| chr9:69873613 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG03491.hp2 HG04184.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-13225G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873613 | |||||||
| chr9:69873660 | A | G | 8 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0239 others(5): Show |
8 | HG00741.hp1 HG01515.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-13178A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873660 | |||||||
| chr9:69873706 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-13132T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873706 | |||||||
| chr9:69873717 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0237 |
2 | HG01934.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.450-13121C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873717 | |||||||
| chr9:69873929 | A | G | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-12909A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873929 | |||||||
| chr9:69873944 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.450-12894C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69873944 | |||||||
| chr9:69874015 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-12823A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874015 | |||||||
| chr9:69874038 | C | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-12800C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874038 | |||||||
| chr9:69874090 | G | A | 31 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0133 others(28): Show |
31 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.450-12748G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874090 | |||||||
| chr9:69874191 | A | AT | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.450-12646dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69874191 | ||||||
| chr9:69874204 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01261.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.450-12634C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874204 | |||||||
| chr9:69874205 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.450-12633G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874205 | |||||||
| chr9:69874257 | G | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0221 |
3 | HG00140.hp2 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.450-12581G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874257 | |||||||
| chr9:69874258 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0221 |
3 | HG00140.hp2 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.450-12580A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874258 | |||||||
| chr9:69874285 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0331 |
3 | NA18945.hp1 NA19005.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.450-12553C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874285 | |||||||
| chr9:69874518 | A | G | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.450-12320A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874518 | |||||||
| chr9:69874608 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.450-12230G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874608 | |||||||
| chr9:69874630 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.450-12208T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874630 | |||||||
| chr9:69874713 | C | T | 4 | a0001c0001t0001g0119 a0001c0002t0001g0297 a0001c0002t0001g0302 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-12125C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874713 | |||||||
| chr9:69874724 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.450-12114T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874724 | |||||||
| chr9:69874892 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.450-11946C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874892 | |||||||
| chr9:69874909 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.450-11929A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69874909 | |||||||
| chr9:69875139 | C | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-11699C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875139 | |||||||
| chr9:69875187 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.450-11651A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875187 | |||||||
| chr9:69875230 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-11608T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875230 | |||||||
| chr9:69875442 | A | G | 1 | a0003c0004t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.450-11396A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875442 | |||||||
| chr9:69875624 | G | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-11214G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875624 | |||||||
| chr9:69875912 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.450-10926A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875912 | |||||||
| chr9:69875971 | T | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0161 a0001c0001t0001g0164 others(5): Show |
8 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-10867T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69875971 | |||||||
| chr9:69876010 | C | T | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-10828C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876010 | |||||||
| chr9:69876011 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.450-10827G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876011 | |||||||
| chr9:69876063 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-10775A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876063 | |||||||
| chr9:69876099 | C | T | 6 | a0001c0002t0001g0022 a0001c0002t0001g0285 a0001c0002t0001g0293 others(3): Show |
6 | HG01069.hp1 HG01261.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-10739C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876099 | |||||||
| chr9:69876124 | A | G | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-10714A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876124 | |||||||
| chr9:69876203 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-10635T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876203 | |||||||
| chr9:69876557 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450-10281A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876557 | |||||||
| chr9:69876784 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.450-10054G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876784 | |||||||
| chr9:69876915 | A | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.450-9923A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69876915 | |||||||
| chr9:69877108 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-9730C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877108 | |||||||
| chr9:69877113 | T | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.450-9725T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877113 | |||||||
| chr9:69877198 | A | G | 1 | a0001c0002t0001g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.450-9640A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877198 | |||||||
| chr9:69877459 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0372 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.450-9379C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877459 | |||||||
| chr9:69877496 | A | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-9342A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877496 | |||||||
| chr9:69877681 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.450-9157A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877681 | |||||||
| chr9:69877707 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.450-9131A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877707 | |||||||
| chr9:69877735 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.450-9103T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877735 | |||||||
| chr9:69877833 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.450-9005T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877833 | |||||||
| chr9:69877861 | G | A | 1 | a0004c0006t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450-8977G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877861 | |||||||
| chr9:69877880 | G | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-8958G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877880 | |||||||
| chr9:69877893 | A | T | 1 | a0001c0001t0001g0014 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.450-8945A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69877893 | |||||||
| chr9:69878043 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.450-8795A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878043 | |||||||
| chr9:69878330 | T | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-8508T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878330 | |||||||
| chr9:69878332 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-8506G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878332 | |||||||
| chr9:69878362 | G | A | 1 | a0004c0006t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450-8476G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878362 | |||||||
| chr9:69878394 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.450-8444T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878394 | |||||||
| chr9:69878582 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.450-8256T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878582 | |||||||
| chr9:69878807 | T | C | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-8031T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878807 | |||||||
| chr9:69878923 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0214 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.450-7915C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878923 | |||||||
| chr9:69878967 | G | A | 1 | a0001c0001t0001g0359 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.450-7871G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878967 | |||||||
| chr9:69878995 | G | A | 1 | a0001c0002t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.450-7843G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69878995 | |||||||
| chr9:69879019 | C | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-7819C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879019 | |||||||
| chr9:69879051 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-7787A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879051 | |||||||
| chr9:69879386 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.450-7452A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879386 | |||||||
| chr9:69879416 | G | A | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-7422G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879416 | |||||||
| chr9:69879471 | A | C | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450-7367A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879471 | |||||||
| chr9:69879480 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-7358G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879480 | |||||||
| chr9:69879496 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450-7342C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879496 | |||||||
| chr9:69879579 | TTAACA | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-7257_450-7253d others(7): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69879579 | ||||||
| chr9:69879606 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.450-7232C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879606 | |||||||
| chr9:69879876 | GT | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.450-6952delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69879876 | ||||||
| chr9:69879915 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.450-6923G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69879915 | |||||||
| chr9:69880051 | G | GAT | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-6786_450-6785d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69880051 | ||||||
| chr9:69880078 | A | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0171 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.450-6760A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880078 | |||||||
| chr9:69880286 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.450-6552T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880286 | |||||||
| chr9:69880366 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | NA18747.hp2 NA18994.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-6472G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880366 | |||||||
| chr9:69880515 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-6323G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880515 | |||||||
| chr9:69880517 | T | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-6321T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880517 | |||||||
| chr9:69880584 | A | G | 1 | a0001c0007t0001g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.450-6254A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880584 | |||||||
| chr9:69880721 | T | C | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-6117T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880721 | |||||||
| chr9:69880805 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-6033A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880805 | |||||||
| chr9:69880936 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.450-5902C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69880936 | |||||||
| chr9:69881004 | A | G | 1 | a0001c0002t0001g0345 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.450-5834A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881004 | |||||||
| chr9:69881230 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-5608G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881230 | |||||||
| chr9:69881265 | C | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-5573C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881265 | |||||||
| chr9:69881359 | G | A | 4 | a0001c0001t0001g0294 a0001c0001t0001g0327 a0001c0001t0001g0341 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-5479G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881359 | |||||||
| chr9:69881413 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-5425A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881413 | |||||||
| chr9:69881461 | A | G | 1 | a0001c0002t0001g0281 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.450-5377A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881461 | |||||||
| chr9:69881478 | G | A | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-5360G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881478 | |||||||
| chr9:69881517 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0220 a0001c0001t0001g0364 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-5321G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881517 | |||||||
| chr9:69881616 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.450-5222C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881616 | |||||||
| chr9:69881663 | A | G | 1 | a0001c0002t0001g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.450-5175A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881663 | |||||||
| chr9:69881746 | G | T | 2 | a0001c0007t0001g0154 a0001c0007t0001g0174 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.450-5092G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881746 | |||||||
| chr9:69881747 | C | T | 2 | a0001c0007t0001g0154 a0001c0007t0001g0174 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.450-5091C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881747 | |||||||
| chr9:69881756 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-5082A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881756 | |||||||
| chr9:69881790 | C | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0054 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.450-5048C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881790 | |||||||
| chr9:69881823 | G | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.450-5015G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69881823 | |||||||
| chr9:69881990 | C | CT | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.450-4836dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69881990 | ||||||
| chr9:69881990 | C | CTT | 9 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0265 others(6): Show |
9 | HG01934.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.450-4837_450-4836d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69881990 | ||||||
| chr9:69882066 | G | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-4772G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69882066 | |||||||
| chr9:69882427 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.450-4411A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69882427 | |||||||
| chr9:69882555 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-4283T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69882555 | |||||||
| chr9:69882918 | A | G | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450-3920A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69882918 | |||||||
| chr9:69883134 | G | C | 1 | a0001c0002t0001g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.450-3704G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883134 | |||||||
| chr9:69883226 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.450-3612G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883226 | |||||||
| chr9:69883233 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0218 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-3605G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883233 | |||||||
| chr9:69883240 | G | C | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.450-3598G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883240 | |||||||
| chr9:69883251 | T | C | 1 | a0001c0002t0001g0307 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.450-3587T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883251 | |||||||
| chr9:69883439 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.450-3399T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883439 | |||||||
| chr9:69883441 | A | T | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-3397A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883441 | |||||||
| chr9:69883553 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
274 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.450-3285C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883553 | |||||||
| chr9:69883597 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.450-3241C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883597 | |||||||
| chr9:69883598 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.450-3240A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883598 | |||||||
| chr9:69883675 | A | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.450-3163A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883675 | |||||||
| chr9:69883822 | T | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0151 a0001c0002t0001g0306 |
3 | HG01169.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.450-3016T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883822 | |||||||
| chr9:69883822 | TA | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
17 | HG00558.hp2 HG01099.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.450-3007delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69883822 | ||||||
| chr9:69883823 | A | T | 1 | a0001c0002t0001g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.450-3015A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883823 | |||||||
| chr9:69883830 | AAC | A | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-3006_450-3005d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69883830 | ||||||
| chr9:69883831 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-3007A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883831 | |||||||
| chr9:69883836 | TA | T | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(348): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.450-2993delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69883836 | ||||||
| chr9:69883836 | TAA | T | 13 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0114 others(10): Show |
13 | HG01243.hp1 HG01496.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.450-2994_450-2993d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69883836 | ||||||
| chr9:69883880 | C | A | 1 | a0002c0003t0001g0245 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.450-2958C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883880 | |||||||
| chr9:69883966 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.450-2872A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883966 | |||||||
| chr9:69883990 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
93 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.450-2848A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69883990 | |||||||
| chr9:69884144 | T | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-2694T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884144 | |||||||
| chr9:69884340 | G | A | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-2498G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884340 | |||||||
| chr9:69884360 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-2478T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884360 | |||||||
| chr9:69884363 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-2475A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884363 | |||||||
| chr9:69884474 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450-2364C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884474 | |||||||
| chr9:69884641 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0304 a0001c0013t0001g0152 |
3 | HG02922.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450-2197C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884641 | |||||||
| chr9:69884660 | G | GT | 181 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(178): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.450-2168dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69884660 | ||||||
| chr9:69884660 | G | GTT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
95 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.450-2169_450-2168d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69884660 | ||||||
| chr9:69884679 | T | C | 1 | a0001c0002t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.450-2159T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884679 | |||||||
| chr9:69884723 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-2115C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69884723 | |||||||
| chr9:69884855 | C | CT | 150 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0052 others(147): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.450-1980dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69884855 | ||||||
| chr9:69884858 | T | TA | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.450-1971dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69884858 | ||||||
| chr9:69885005 | T | C | 1 | a0004c0006t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450-1833T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885005 | |||||||
| chr9:69885026 | A | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.450-1812A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885026 | |||||||
| chr9:69885289 | TAATATTG others(5): Show |
T | 118 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0088 others(115): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.450-1545_450-1534d others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 69885289 | ||||||
| chr9:69885292 | T | C | 1 | a0001c0007t0001g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.450-1546T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885292 | |||||||
| chr9:69885463 | T | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0220 a0001c0001t0001g0364 others(1): Show |
4 | HG01891.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-1375T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885463 | |||||||
| chr9:69885547 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-1291A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885547 | |||||||
| chr9:69885655 | C | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
13 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.450-1183C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885655 | |||||||
| chr9:69885693 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.450-1145T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885693 | |||||||
| chr9:69885739 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0093 others(27): Show |
31 | HG00099.hp2 HG00609.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.450-1099C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885739 | |||||||
| chr9:69885740 | G | A | 2 | a0001c0002t0001g0147 a0001c0002t0001g0148 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.450-1098G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885740 | |||||||
| chr9:69885790 | G | T | 1 | a0001c0001t0001g0341 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.450-1048G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885790 | |||||||
| chr9:69885991 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.450-847T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69885991 | |||||||
| chr9:69886019 | C | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
274 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.450-819C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886019 | |||||||
| chr9:69886040 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.450-798T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886040 | |||||||
| chr9:69886229 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.450-609G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886229 | |||||||
| chr9:69886348 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.450-490G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886348 | |||||||
| chr9:69886461 | T | C | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.450-377T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886461 | |||||||
| chr9:69886529 | G | A | 146 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0088 others(143): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.450-309G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886529 | |||||||
| chr9:69886539 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
94 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.450-299A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886539 | |||||||
| chr9:69886543 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.450-295G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886543 | |||||||
| chr9:69886675 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.450-163C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886675 | |||||||
| chr9:69886744 | A | T | 1 | a0001c0001t0001g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.450-94A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886744 | |||||||
| chr9:69886782 | G | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
306 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.450-56G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886782 | |||||||
| chr9:69886822 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.450-16G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 4/5 | chr9 | 69886822 | |||||||
| chr9:69886959 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.507+64A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69886959 | |||||||
| chr9:69887046 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+151T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887046 | |||||||
| chr9:69887108 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.507+213C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887108 | |||||||
| chr9:69887192 | C | A | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.507+297C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887192 | |||||||
| chr9:69887416 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.507+521T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887416 | |||||||
| chr9:69887532 | T | C | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.507+637T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887532 | |||||||
| chr9:69887569 | C | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+674C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887569 | |||||||
| chr9:69887860 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+965G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887860 | |||||||
| chr9:69887937 | G | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+1042G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69887937 | |||||||
| chr9:69888061 | G | A | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+1166G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888061 | |||||||
| chr9:69888153 | G | T | 31 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.507+1258G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888153 | |||||||
| chr9:69888165 | A | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+1270A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888165 | |||||||
| chr9:69888516 | C | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.507+1621C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888516 | |||||||
| chr9:69888589 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+1694C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888589 | |||||||
| chr9:69888667 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+1772G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888667 | |||||||
| chr9:69888695 | G | A | 1 | a0003c0004t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.507+1800G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888695 | |||||||
| chr9:69888885 | G | GA | 171 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0039 others(168): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.507+2002dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69888885 | ||||||
| chr9:69888885 | G | GAA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
103 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.507+2001_507+2002d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69888885 | ||||||
| chr9:69888958 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2063A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69888958 | |||||||
| chr9:69889187 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+2292T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889187 | |||||||
| chr9:69889232 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.507+2337C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889232 | |||||||
| chr9:69889483 | C | T | 2 | a0001c0001t0001g0087 a0003c0004t0001g0089 |
2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.507+2588C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889483 | |||||||
| chr9:69889526 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
253 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.507+2631T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889526 | |||||||
| chr9:69889566 | C | G | 1 | a0003c0004t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.507+2671C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889566 | |||||||
| chr9:69889609 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+2714G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69889609 | |||||||
| chr9:69890123 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+3228T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890123 | |||||||
| chr9:69890135 | G | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.507+3240G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890135 | |||||||
| chr9:69890150 | A | C | 1 | a0001c0005t0001g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.507+3255A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890150 | |||||||
| chr9:69890434 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
107 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.507+3539T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890434 | |||||||
| chr9:69890443 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.507+3548C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890443 | |||||||
| chr9:69890668 | C | T | 48 | a0001c0001t0001g0086 a0001c0001t0001g0097 a0001c0001t0001g0116 others(45): Show |
48 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.507+3773C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890668 | |||||||
| chr9:69890669 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+3774G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890669 | |||||||
| chr9:69890789 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+3894G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890789 | |||||||
| chr9:69890859 | C | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
13 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+3964C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890859 | |||||||
| chr9:69890894 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 |
3 | HG01099.hp1 HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.507+3999A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890894 | |||||||
| chr9:69890897 | A | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+4002A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890897 | |||||||
| chr9:69890948 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.507+4053C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69890948 | |||||||
| chr9:69891018 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.507+4123C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891018 | |||||||
| chr9:69891035 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4140T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891035 | |||||||
| chr9:69891064 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(19): Show |
22 | HG01099.hp1 HG01361.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.507+4169G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891064 | |||||||
| chr9:69891081 | G | A | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.507+4186G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891081 | |||||||
| chr9:69891150 | A | G | 1 | a0001c0005t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+4255A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891150 | |||||||
| chr9:69891168 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.507+4273G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891168 | |||||||
| chr9:69891213 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+4318C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891213 | |||||||
| chr9:69891334 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.507+4439C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891334 | |||||||
| chr9:69891346 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.507+4451G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891346 | |||||||
| chr9:69891370 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.507+4475C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891370 | |||||||
| chr9:69891384 | G | A | 145 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0088 others(142): Show |
146 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.507+4489G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891384 | |||||||
| chr9:69891428 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
308 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.507+4533G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891428 | |||||||
| chr9:69891500 | C | CT | 34 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(31): Show |
34 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.507+4618dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69891500 | ||||||
| chr9:69891500 | CT | C | 123 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0077 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.507+4618delT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69891500 | ||||||
| chr9:69891672 | T | C | 1 | a0001c0001t0001g0359 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.507+4777T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891672 | |||||||
| chr9:69891982 | G | A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0218 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+5087G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69891982 | |||||||
| chr9:69892143 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
274 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.507+5248G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892143 | |||||||
| chr9:69892329 | G | A | 1 | a0002c0003t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.507+5434G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892329 | |||||||
| chr9:69892356 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0364 a0001c0001t0001g0365 |
3 | HG01891.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.507+5461T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892356 | |||||||
| chr9:69892405 | G | A | 1 | a0001c0002t0001g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.507+5510G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892405 | |||||||
| chr9:69892583 | G | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0054 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.507+5688G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892583 | |||||||
| chr9:69892625 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.507+5730T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892625 | |||||||
| chr9:69892745 | A | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.507+5850A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892745 | |||||||
| chr9:69892745 | A | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0150 a0001c0001t0001g0171 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+5850A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892745 | |||||||
| chr9:69892765 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.507+5870T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892765 | |||||||
| chr9:69892796 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
94 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.507+5901A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892796 | |||||||
| chr9:69892947 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.507+6052A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69892947 | |||||||
| chr9:69893080 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.507+6185T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893080 | |||||||
| chr9:69893177 | A | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+6282A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893177 | |||||||
| chr9:69893217 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+6322A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893217 | |||||||
| chr9:69893386 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+6491A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893386 | |||||||
| chr9:69893464 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+6569T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893464 | |||||||
| chr9:69893495 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+6600T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893495 | |||||||
| chr9:69893513 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(2): Show |
5 | HG01496.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+6618G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893513 | |||||||
| chr9:69893637 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.507+6742A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893637 | |||||||
| chr9:69893682 | A | C | 1 | a0001c0001t0001g0370 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+6787A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893682 | |||||||
| chr9:69893830 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+6935C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893830 | |||||||
| chr9:69893866 | C | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
13 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+6971C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69893866 | |||||||
| chr9:69894048 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.507+7153A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69894048 | |||||||
| chr9:69894212 | A | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+7317A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69894212 | |||||||
| chr9:69894607 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(5): Show |
8 | HG01099.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+7712A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69894607 | |||||||
| chr9:69894650 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.507+7755G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69894650 | |||||||
| chr9:69894990 | CA | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
265 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.507+8104delA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69894990 | ||||||
| chr9:69894998 | AAG | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(36): Show |
39 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.507+8105_507+8106d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69894998 | ||||||
| chr9:69894999 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0219 a0001c0001t0001g0318 |
3 | HG02965.hp1 HG06807.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.507+8104A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69894999 | |||||||
| chr9:69895000 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0219 a0001c0001t0001g0315 others(1): Show |
4 | HG02965.hp1 HG06807.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+8105G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895000 | |||||||
| chr9:69895001 | A | G | 39 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(36): Show |
39 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.507+8106A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895001 | |||||||
| chr9:69895119 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.507+8224T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895119 | |||||||
| chr9:69895275 | A | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.507+8380A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895275 | |||||||
| chr9:69895335 | G | GTC | 12 | a0001c0001t0001g0201 a0001c0001t0001g0222 a0001c0001t0001g0223 others(9): Show |
12 | HG00621.hp1 HG01175.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.507+8474_507+8475d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | G | GTCTCTC | 36 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0097 others(33): Show |
37 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.507+8470_507+8475d others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | G | GTCTCTCT others(1): Show |
4 | a0001c0001t0001g0181 a0001c0001t0001g0214 a0001c0001t0001g0264 others(1): Show |
4 | HG03225.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+8468_507+8475d others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | G | GTCTCTCT others(3): Show |
4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0271 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+8466_507+8475d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | GTC | G | 5 | a0001c0001t0001g0231 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02109.hp1 HG02976.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+8474_507+8475d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | GTCTCTC | G | 29 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+8470_507+8475d others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895335 | GTCTCTCT others(1): Show |
G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+8468_507+8475d others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895335 | ||||||
| chr9:69895361 | C | CTGTGTG | 6 | a0001c0001t0001g0007 a0001c0001t0001g0356 a0001c0001t0001g0359 others(3): Show |
6 | HG02257.hp1 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+8467_507+8468i others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895361 | ||||||
| chr9:69895361 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.507+8467_507+8468i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895361 | ||||||
| chr9:69895361 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.507+8466C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895361 | |||||||
| chr9:69895363 | C | CTGTGTG | 4 | a0001c0001t0003g0360 a0001c0002t0001g0290 a0001c0002t0001g0328 others(1): Show |
4 | HG02056.hp1 HG02717.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+8469_507+8470i others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895363 | ||||||
| chr9:69895363 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0366 others(2): Show |
5 | HG02074.hp1 HG02132.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+8469_507+8470i others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895363 | ||||||
| chr9:69895363 | C | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0110 a0001c0001t0001g0150 others(11): Show |
14 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.507+8468C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895363 | |||||||
| chr9:69895365 | C | CTGTGTG | 7 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0076 others(4): Show |
7 | HG01175.hp2 HG01255.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+8471_507+8472i others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895365 | ||||||
| chr9:69895365 | C | CTGTGTGT others(1): Show |
48 | a0001c0001t0001g0088 a0001c0001t0001g0119 a0001c0001t0001g0364 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.507+8471_507+8472i others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895365 | ||||||
| chr9:69895365 | C | CTGTGTGT others(3): Show |
15 | a0001c0002t0001g0011 a0001c0002t0001g0252 a0001c0002t0001g0253 others(12): Show |
15 | HG02523.hp1 HG03831.hp1 NA18941.hp1 others(12): Show |
intron_variant | MODIFIER | c.507+8471_507+8472i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895365 | ||||||
| chr9:69895365 | C | CTGTGTGT others(5): Show |
1 | a0001c0002t0001g0326 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.507+8471_507+8472i others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895365 | ||||||
| chr9:69895365 | C | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(21): Show |
24 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.507+8470C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895365 | |||||||
| chr9:69895367 | C | CTGTGTGT others(1): Show |
20 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(17): Show |
20 | HG01243.hp2 HG01943.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.507+8473_507+8474i others(10): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895367 | ||||||
| chr9:69895367 | C | CTGTGTGT others(3): Show |
2 | a0001c0002t0001g0301 a0001c0002t0001g0305 |
2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.507+8473_507+8474i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895367 | ||||||
| chr9:69895367 | C | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0043 others(98): Show |
102 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.507+8472C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895367 | |||||||
| chr9:69895369 | C | CTCTCTCT others(9): Show |
1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.507+8475_507+8476i others(24): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.507+8475_507+8476i others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0001g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.507+8475_507+8476i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(9): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0179 a0001c0001t0001g0185 others(2): Show |
5 | HG03942.hp1 HG04184.hp1 NA19090.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+8475_507+8476i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTG | 3 | a0001c0001t0001g0206 a0001c0001t0001g0210 a0001c0001t0001g0342 |
3 | NA18965.hp2 NA18989.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.507+8475_507+8476i others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTGT others(5): Show |
1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.507+8475_507+8476i others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTGT others(7): Show |
19 | a0001c0001t0001g0133 a0001c0001t0001g0180 a0001c0001t0001g0182 others(16): Show |
19 | HG00544.hp1 HG00597.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.507+8475_507+8476i others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTCTGT others(9): Show |
13 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+8475_507+8476i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTGTGT others(3): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0042 others(2): Show |
8 | HG03927.hp1 NA18965.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+8475_507+8476i others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTGTGT others(5): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0348 a0001c0002t0001g0103 |
3 | HG01256.hp2 HG02132.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.507+8475_507+8476i others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTGTGT others(7): Show |
1 | a0001c0001t0001g0327 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTGTGT others(9): Show |
1 | a0001c0002t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(18): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTCTGTGT others(11): Show |
1 | a0001c0002t0001g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+8475_507+8476i others(20): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTGTGTGT others(3): Show |
69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
72 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.507+8492_507+8501d others(12): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTGTGTGT others(5): Show |
6 | a0001c0001t0001g0220 a0001c0002t0001g0145 a0001c0002t0001g0147 others(3): Show |
6 | HG00738.hp2 HG01074.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+8490_507+8501d others(14): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0197 |
2 | HG01361.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.507+8488_507+8501d others(16): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895369 | C | G | 150 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0021 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.507+8474C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895369 | |||||||
| chr9:69895369 | CTGTGTG | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0304 others(1): Show |
4 | HG01496.hp2 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+8496_507+8501d others(8): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69895369 | ||||||
| chr9:69895371 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(3): Show |
6 | HG01099.hp1 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+8476G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895371 | |||||||
| chr9:69895373 | G | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0008c0014t0001g0173 |
3 | HG02055.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.507+8478G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895373 | |||||||
| chr9:69895481 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.507+8586T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895481 | |||||||
| chr9:69895727 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.507+8832G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895727 | |||||||
| chr9:69895750 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.507+8855C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895750 | |||||||
| chr9:69895841 | A | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0046 others(18): Show |
21 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+8946A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895841 | |||||||
| chr9:69895953 | G | C | 31 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.507+9058G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69895953 | |||||||
| chr9:69896077 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.507+9182A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896077 | |||||||
| chr9:69896090 | G | A | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.507+9195G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896090 | |||||||
| chr9:69896225 | C | T | 1 | a0001c0002t0001g0339 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.507+9330C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896225 | |||||||
| chr9:69896226 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0135 others(17): Show |
20 | HG01496.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+9331G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896226 | |||||||
| chr9:69896401 | T | A | 1 | a0001c0005t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+9506T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896401 | |||||||
| chr9:69896545 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-9409C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896545 | |||||||
| chr9:69896762 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.508-9192C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896762 | |||||||
| chr9:69896984 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(5): Show |
9 | HG00438.hp1 HG02040.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-8970T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69896984 | |||||||
| chr9:69897066 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.508-8888A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897066 | |||||||
| chr9:69897100 | G | A | 1 | a0006c0011t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.508-8854G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897100 | |||||||
| chr9:69897282 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0347 |
3 | HG02976.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.508-8672G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897282 | |||||||
| chr9:69897300 | G | T | 33 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(30): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.508-8654G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897300 | |||||||
| chr9:69897376 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0074 others(40): Show |
43 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.508-8578T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897376 | |||||||
| chr9:69897421 | G | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0029 others(2): Show |
6 | HG00639.hp2 HG00673.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-8533G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897421 | |||||||
| chr9:69897600 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.508-8354G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897600 | |||||||
| chr9:69897741 | G | C | 1 | a0004c0006t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.508-8213G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897741 | |||||||
| chr9:69897749 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0347 others(1): Show |
4 | HG02976.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-8205A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897749 | |||||||
| chr9:69897761 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0031 others(2): Show |
8 | HG00597.hp2 NA18965.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.508-8193G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897761 | |||||||
| chr9:69897982 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.508-7972A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69897982 | |||||||
| chr9:69898119 | G | GA | 84 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0033 others(81): Show |
85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-7831dupA | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69898119 | ||||||
| chr9:69898217 | G | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0239 others(4): Show |
7 | HG00741.hp1 HG01074.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-7737G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898217 | |||||||
| chr9:69898324 | A | G | 33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(30): Show |
33 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.508-7630A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898324 | |||||||
| chr9:69898365 | C | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0304 a0001c0002t0001g0172 others(5): Show |
8 | HG01496.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.508-7589C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898365 | |||||||
| chr9:69898417 | C | G | 1 | a0001c0001t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-7537C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898417 | |||||||
| chr9:69898462 | G | A | 1 | a0001c0001t0001g0355 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-7492G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898462 | |||||||
| chr9:69898676 | C | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-7278C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898676 | |||||||
| chr9:69898689 | C | T | 100 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0028 others(97): Show |
100 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.508-7265C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898689 | |||||||
| chr9:69898703 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0294 a0001c0001t0001g0327 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-7251A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898703 | |||||||
| chr9:69898708 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-7246G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898708 | |||||||
| chr9:69898870 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.508-7084C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898870 | |||||||
| chr9:69898971 | C | G | 1 | a0001c0001t0001g0346 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508-6983C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69898971 | |||||||
| chr9:69899194 | T | C | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.508-6760T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899194 | |||||||
| chr9:69899261 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.508-6693A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899261 | |||||||
| chr9:69899395 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.508-6559A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899395 | |||||||
| chr9:69899516 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.508-6438T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899516 | |||||||
| chr9:69899564 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0219 a0003c0004t0001g0141 |
3 | HG02451.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.508-6390C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899564 | |||||||
| chr9:69899603 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0102 others(5): Show |
9 | HG00099.hp1 HG00099.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-6351A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899603 | |||||||
| chr9:69899617 | C | A | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-6337C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899617 | |||||||
| chr9:69899775 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0002c0003t0001g0248 |
3 | HG00673.hp1 HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.508-6179A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899775 | |||||||
| chr9:69899968 | A | T | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-5986A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69899968 | |||||||
| chr9:69900004 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.508-5950C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900004 | |||||||
| chr9:69900020 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.508-5934A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900020 | |||||||
| chr9:69900162 | C | A | 205 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(202): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.508-5792C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900162 | |||||||
| chr9:69900187 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0149 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-5767A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900187 | |||||||
| chr9:69900237 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.508-5717C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900237 | |||||||
| chr9:69900356 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0149 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-5598A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900356 | |||||||
| chr9:69900425 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.508-5529C>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900425 | |||||||
| chr9:69900474 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.508-5480T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900474 | |||||||
| chr9:69900686 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.508-5268T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69900686 | |||||||
| chr9:69901012 | C | T | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-4942C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901012 | |||||||
| chr9:69901018 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(36): Show |
40 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.508-4936C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901018 | |||||||
| chr9:69901072 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.508-4882T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901072 | |||||||
| chr9:69901142 | G | GT | 31 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.508-4799dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69901142 | ||||||
| chr9:69901142 | G | GTT | 7 | a0001c0001t0001g0030 a0001c0001t0001g0149 a0001c0001t0001g0155 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-4800_508-4799d others(4): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69901142 | ||||||
| chr9:69901177 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG02486.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-4777G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901177 | |||||||
| chr9:69901218 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(65): Show |
74 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.508-4736A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901218 | |||||||
| chr9:69901239 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG03209.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.508-4715G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901239 | |||||||
| chr9:69901246 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.508-4708T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901246 | |||||||
| chr9:69901262 | C | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0347 |
3 | HG02976.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.508-4692C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901262 | |||||||
| chr9:69901304 | A | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-4650A>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901304 | |||||||
| chr9:69901313 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0005c0010t0001g0020 |
3 | HG00639.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.508-4641A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901313 | |||||||
| chr9:69901372 | C | T | 7 | a0001c0001t0001g0294 a0001c0001t0001g0327 a0001c0001t0001g0341 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-4582C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901372 | |||||||
| chr9:69901426 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(158): Show |
163 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.508-4528C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901426 | |||||||
| chr9:69901437 | G | A | 2 | a0001c0001t0001g0219 a0003c0004t0001g0141 |
2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.508-4517G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901437 | |||||||
| chr9:69901459 | C | T | 7 | a0001c0001t0001g0294 a0001c0001t0001g0327 a0001c0001t0001g0341 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-4495C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901459 | |||||||
| chr9:69901521 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0149 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-4433C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901521 | |||||||
| chr9:69901525 | C | CT | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-4424dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69901525 | ||||||
| chr9:69901527 | T | TTTTATGG others(42): Show |
1 | a0001c0001t0001g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.508-4425_508-4377d others(51): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69901527 | ||||||
| chr9:69901556 | A | G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(17): Show |
20 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-4398A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901556 | |||||||
| chr9:69901631 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
62 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.508-4323A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901631 | |||||||
| chr9:69901769 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0187 |
2 | HG00423.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.508-4185C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901769 | |||||||
| chr9:69901818 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.508-4136G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901818 | |||||||
| chr9:69901877 | C | A | 2 | a0001c0001t0001g0140 a0003c0004t0001g0090 |
2 | HG01496.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.508-4077C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901877 | |||||||
| chr9:69901886 | T | C | 126 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0045 others(123): Show |
127 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.508-4068T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901886 | |||||||
| chr9:69901921 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0136 |
2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.508-4033A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901921 | |||||||
| chr9:69901943 | T | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0033 others(51): Show |
54 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.508-4011T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901943 | |||||||
| chr9:69901957 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.508-3997T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69901957 | |||||||
| chr9:69902127 | A | G | 1 | a0002c0008t0001g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.508-3827A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902127 | |||||||
| chr9:69902246 | T | C | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-3708T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902246 | |||||||
| chr9:69902254 | G | C | 2 | a0001c0002t0001g0232 a0001c0002t0001g0234 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.508-3700G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902254 | |||||||
| chr9:69902305 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.508-3649T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902305 | |||||||
| chr9:69902329 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.508-3625A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902329 | |||||||
| chr9:69902352 | C | T | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3602C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902352 | |||||||
| chr9:69902377 | G | T | 27 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.508-3577G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902377 | |||||||
| chr9:69902454 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.508-3500G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902454 | |||||||
| chr9:69902546 | T | G | 1 | a0001c0002t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508-3408T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902546 | |||||||
| chr9:69902554 | C | T | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3400C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902554 | |||||||
| chr9:69902615 | A | G | 4 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0001c0001t0001g0222 others(1): Show |
4 | HG00558.hp1 NA18950.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3339A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902615 | |||||||
| chr9:69902679 | G | GT | 7 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0179 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-3264dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69902679 | ||||||
| chr9:69902763 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.508-3191C>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902763 | |||||||
| chr9:69902812 | CTCCTATT others(42): Show |
C | 1 | a0001c0001t0001g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.508-3141_508-3093d others(51): Show |
CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902812 | |||||||
| chr9:69902949 | C | T | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-3005C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902949 | |||||||
| chr9:69902970 | G | C | 4 | a0001c0001t0001g0327 a0001c0001t0001g0359 a0001c0001t0001g0369 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-2984G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69902970 | |||||||
| chr9:69903008 | G | A | 2 | a0001c0001t0001g0140 a0003c0004t0001g0090 |
2 | HG01496.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.508-2946G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903008 | |||||||
| chr9:69903050 | T | C | 1 | a0008c0014t0001g0173 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508-2904T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903050 | |||||||
| chr9:69903411 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.508-2543C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903411 | |||||||
| chr9:69903455 | C | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0239 a0001c0001t0001g0242 others(4): Show |
7 | HG00738.hp2 HG01070.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-2499C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903455 | |||||||
| chr9:69903564 | T | C | 1 | a0001c0002t0001g0333 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.508-2390T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903564 | |||||||
| chr9:69903671 | C | T | 27 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.508-2283C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903671 | |||||||
| chr9:69903719 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.508-2235A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903719 | |||||||
| chr9:69903850 | A | C | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-2104A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903850 | |||||||
| chr9:69903868 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.508-2086A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903868 | |||||||
| chr9:69903874 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.508-2080G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903874 | |||||||
| chr9:69903876 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.508-2078G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903876 | |||||||
| chr9:69903915 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508-2039G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903915 | |||||||
| chr9:69903963 | A | C | 6 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0121 others(3): Show |
6 | HG00639.hp1 HG01358.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-1991A>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69903963 | |||||||
| chr9:69904004 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.508-1950G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904004 | |||||||
| chr9:69904081 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.508-1873C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904081 | |||||||
| chr9:69904173 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-1781C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904173 | |||||||
| chr9:69904196 | C | T | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1758C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904196 | |||||||
| chr9:69904197 | A | G | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1757A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904197 | |||||||
| chr9:69904255 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.508-1699G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904255 | |||||||
| chr9:69904256 | T | C | 27 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0091 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.508-1698T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904256 | |||||||
| chr9:69904415 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.508-1539C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904415 | |||||||
| chr9:69904503 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-1451T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904503 | |||||||
| chr9:69904546 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.508-1408G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904546 | |||||||
| chr9:69904614 | A | G | 1 | a0001c0002t0001g0345 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.508-1340A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904614 | |||||||
| chr9:69904635 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
63 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.508-1319C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904635 | |||||||
| chr9:69904787 | G | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(160): Show |
165 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.508-1167G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904787 | |||||||
| chr9:69904826 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508-1128A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904826 | |||||||
| chr9:69904997 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508-957A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69904997 | |||||||
| chr9:69905160 | T | A | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-794T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905160 | |||||||
| chr9:69905232 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.508-722C>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905232 | |||||||
| chr9:69905289 | G | T | 1 | a0001c0001t0001g0348 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.508-665G>T | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905289 | |||||||
| chr9:69905333 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.508-621G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905333 | |||||||
| chr9:69905354 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
166 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.508-600G>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905354 | |||||||
| chr9:69905354 | G | C | 1 | a0003c0004t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.508-600G>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905354 | |||||||
| chr9:69905509 | T | A | 2 | a0001c0002t0001g0068 a0001c0002t0001g0069 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.508-445T>A | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905509 | |||||||
| chr9:69905613 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.508-341T>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905613 | |||||||
| chr9:69905622 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG03486.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.508-332A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905622 | |||||||
| chr9:69905640 | C | CT | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-313dupT | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 69905640 | ||||||
| chr9:69905654 | A | G | 28 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.508-300A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905654 | |||||||
| chr9:69905709 | T | C | 35 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0048 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.508-245T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905709 | |||||||
| chr9:69905907 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.508-47T>C | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905907 | |||||||
| chr9:69905922 | A | G | 3 | a0001c0001t0001g0355 a0001c0002t0001g0232 a0001c0002t0001g0234 |
3 | HG02615.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-32A>G | CFAP95 | ENSG00000204711.9 | transcript | ENST00000377197.8 | protein_coding | 5/5 | chr9 | 69905922 |