Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154313 |
| ensemblid | ENSG00000272514.6 |
| hgncid | 21405 |
| symbol | CFAP206 |
| name | cilia and flagella associated protein 206 |
| refseq_nuc | NM_001031743.3 |
| refseq_prot | NP_001026913.1 |
| ensembl_nuc | ENST00000369562.9 |
| ensembl_prot | ENSP00000358575.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 87407972 |
| end | 87464465 |
| strand | + |
| ver | v1.2 |
| region | chr6:87407972-87464465 |
| region5000 | chr6:87402972-87469465 |
| regionname0 | CFAP206_chr6_87407972_87464465 |
| regionname5000 | CFAP206_chr6_87402972_87469465 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 622 | 317 | 70 | 65 | 136 | 16 | 29 | 105 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0002 | 0/1 | 622 | 35 | 7 | 7 | 17 | 1 | 2 | 14 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0003 | 0/0 | 622 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0004 | 0/0 | 622 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0005 | 0/0 | 622 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0006 | 0/0 | 622 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0007 | 0/0 | 622 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0008 | 0/0 | 622 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0009 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0010 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0011 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0012 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| a0013 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | MPPTQ others(617): Show |
chr6 | 87402972 | 87469465 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1866 | 289 | 64 | 64 | 119 | 14 | 27 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0001c0003 | 0/0 | 1866 | 22 | 0 | 1 | 17 | 2 | 2 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0001c0007 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0001c0008 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0001c0014 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0002c0002 | 0/1 | 1866 | 35 | 7 | 7 | 17 | 1 | 2 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0003c0004 | 0/0 | 1866 | 5 | 3 | 2 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0004c0005 | 0/0 | 1866 | 4 | 0 | 1 | 0 | 0 | 3 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0005c0006 | 0/0 | 1866 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0006c0009 | 0/0 | 1866 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0007c0011 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0008c0010 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0009c0013 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0010c0012 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0011c0016 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0012c0017 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 | ||
| a0013c0015 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | ATGCC others(1861): Show |
chr6 | 87402972 | 87469465 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2207 | 176 | 44 | 36 | 70 | 10 | 15 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0001t0002 | 0/0 | 2207 | 100 | 8 | 27 | 49 | 4 | 12 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0001t0003 | 0/0 | 2207 | 9 | 9 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0001t0004 | 0/0 | 2207 | 4 | 3 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0003t0001 | 0/0 | 2207 | 22 | 0 | 1 | 17 | 2 | 2 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0007t0001 | 0/0 | 2207 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0008t0002 | 0/0 | 2207 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0001c0014t0002 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0002c0002t0001 | 0/0 | 2207 | 33 | 6 | 7 | 17 | 1 | 2 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0002c0002t0002 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0002c0002t0005 | 0/1 | 2207 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0003c0004t0001 | 0/0 | 2207 | 5 | 3 | 2 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0004c0005t0001 | 0/0 | 2207 | 4 | 0 | 1 | 0 | 0 | 3 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0005c0006t0002 | 0/0 | 2207 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0006c0009t0002 | 0/0 | 2207 | 2 | 0 | 1 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0007c0011t0001 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0007c0011t0002 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0008c0010t0001 | 0/0 | 2207 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0009c0013t0001 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0010c0012t0002 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0011c0016t0001 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0012c0017t0001 | 0/0 | 2207 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| a0013c0015t0001 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | CTTCC others(2202): Show |
chr6 | 87402972 | 87469465 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0007t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0007t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0008t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0008t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0001c0014t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0002c0002t0005g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0003c0004t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0003c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0003c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0003c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0004c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0004c0005t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0004c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0004c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0005c0006t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0005c0006t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0005c0006t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0005c0006t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0006c0009t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0006c0009t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0007c0011t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0007c0011t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0008c0010t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0008c0010t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0009c0013t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0010c0012t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0011c0016t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0012c0017t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| a0013c0015t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00099 | hp2 | a0006 | c0009 | t0002 | g0104 | EUR | GBR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0265 | EUR | FIN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | FIN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00438 | hp1 | a0009 | c0013 | t0001 | g0126 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0020 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01243 | hp1 | a0006 | c0009 | t0002 | g0069 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01358 | hp2 | a0003 | c0004 | t0001 | g0245 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0121 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01884 | hp1 | a0007 | c0011 | t0002 | g0227 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01934 | hp1 | a0004 | c0005 | t0001 | g0261 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02145 | hp2 | a0008 | c0010 | t0001 | g0255 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | CDX | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CDX | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02257 | hp1 | a0001 | c0007 | t0001 | g0240 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02523 | hp1 | a0010 | c0012 | t0002 | g0108 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | KHV | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02622 | hp1 | a0001 | c0007 | t0001 | g0246 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0254 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02738 | hp2 | a0004 | c0005 | t0001 | g0260 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0239 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0257 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02965 | hp2 | a0003 | c0004 | t0001 | g0020 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02970 | hp1 | a0007 | c0011 | t0001 | g0228 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03041 | hp2 | a0011 | c0016 | t0001 | g0327 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03195 | hp2 | a0001 | c0014 | t0002 | g0025 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03579 | hp1 | a0012 | c0017 | t0001 | g0340 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0262 | SAS | PJL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03927 | hp2 | a0004 | c0005 | t0001 | g0263 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0274 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | STU | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18949 | hp1 | a0005 | c0006 | t0002 | g0055 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18966 | hp1 | a0005 | c0006 | t0002 | g0032 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19005 | hp2 | a0013 | c0015 | t0001 | g0219 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19006 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19043 | hp2 | a0001 | c0008 | t0002 | g0247 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19070 | hp2 | a0005 | c0006 | t0002 | g0059 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19075 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19086 | hp1 | a0005 | c0006 | t0002 | g0068 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0244 | AFR | YRI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20129 | hp1 | a0008 | c0010 | t0001 | g0256 | AFR | ASW | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ASW | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0196 | EUR | TSI | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0171 | SAS | GIH | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0243 | AFR | ACB | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20300 | hp1 | a0001 | c0008 | t0002 | g0026 | AFR | USA | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | USA | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | LWK | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0005 | g0248 | REF | REF | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0138 | REF | REF | CFAP206_chr6_87402972_87469465 | CFAP206 | chr6 | 87402972 | 87469465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87413831 | G | A | 1 | a0006 | 2 | HG00099.hp2 HG01243.hp1 |
missense_variant | MODERATE | c.214G>A | p.Asp72Asn | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/13 | 337/2207 | 214/1869 | 72/622 | chr6 | 87413831 | |||
| chr6:87415824 | G | A | 3 | a0002 a0004 a0008 |
40 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
missense_variant | MODERATE | c.422G>A | p.Arg141His | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/13 | 545/2207 | 422/1869 | 141/622 | chr6 | 87415824 | |||
| chr6:87415863 | G | A | 1 | a0003 | 5 | HG00741.hp1 HG01358.hp2 HG02559.hp2 others(2): Show |
missense_variant | MODERATE | c.461G>A | p.Arg154Lys | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/13 | 584/2207 | 461/1869 | 154/622 | chr6 | 87415863 | |||
| chr6:87416705 | G | C | 2 | a0002 a0004 |
38 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
missense_variant | MODERATE | c.509G>C | p.Gly170Ala | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/13 | 632/2207 | 509/1869 | 170/622 | chr6 | 87416705 | |||
| chr6:87416740 | C | T | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.544C>T | p.Arg182Cys | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/13 | 667/2207 | 544/1869 | 182/622 | chr6 | 87416740 | |||
| chr6:87418264 | C | T | 1 | a0011 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.688C>T | p.Leu230Phe | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/13 | 811/2207 | 688/1869 | 230/622 | chr6 | 87418264 | |||
| chr6:87418277 | G | A | 1 | a0010 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.701G>A | p.Arg234Gln | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/13 | 824/2207 | 701/1869 | 234/622 | chr6 | 87418277 | |||
| chr6:87418336 | A | G | 1 | a0005 | 4 | NA18949.hp1 NA18966.hp1 NA19070.hp2 others(1): Show |
missense_variant | MODERATE | c.760A>G | p.Arg254Gly | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/13 | 883/2207 | 760/1869 | 254/622 | chr6 | 87418336 | |||
| chr6:87418379 | A | G | 1 | a0007 | 2 | HG01884.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.803A>G | p.Asn268Ser | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/13 | 926/2207 | 803/1869 | 268/622 | chr6 | 87418379 | |||
| chr6:87426556 | G | A | 1 | a0009 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.871G>A | p.Glu291Lys | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/13 | 994/2207 | 871/1869 | 291/622 | chr6 | 87426556 | |||
| chr6:87426587 | T | G | 1 | a0009 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.902T>G | p.Leu301Arg | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/13 | 1025/2207 | 902/1869 | 301/622 | chr6 | 87426587 | |||
| chr6:87428641 | C | T | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.976C>T | p.Leu326Phe | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/13 | 1099/2207 | 976/1869 | 326/622 | chr6 | 87428641 | |||
| chr6:87431093 | C | A | 1 | a0004 | 4 | HG01934.hp1 HG02738.hp2 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.1220C>A | p.Ala407Glu | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/13 | 1343/2207 | 1220/1869 | 407/622 | chr6 | 87431093 | |||
| chr6:87461042 | T | A | 1 | a0013 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.1515T>A | p.His505Gln | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/13 | 1638/2207 | 1515/1869 | 505/622 | chr6 | 87461042 | |||
| chr6:87464131 | A | T | 1 | a0008 | 2 | HG02145.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1750A>T | p.Arg584Trp | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 13/13 | 1873/2207 | 1750/1869 | 584/622 | chr6 | 87464131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87409845 | T | G | 1 | a0001c0008 | 2 | NA19043.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.6T>G | p.Pro2Pro | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/13 | 129/2207 | 6/1869 | 2/622 | chr6 | 87409845 | |||
| chr6:87418371 | G | A | 2 | a0001c0007 a0003c0004 |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
synonymous_variant | LOW | c.795G>A | p.Ala265Ala | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/13 | 918/2207 | 795/1869 | 265/622 | chr6 | 87418371 | |||
| chr6:87426606 | C | T | 2 | a0001c0003 a0013c0015 |
23 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(20): Show |
synonymous_variant | LOW | c.921C>T | p.Thr307Thr | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/13 | 1044/2207 | 921/1869 | 307/622 | chr6 | 87426606 | |||
| chr6:87428736 | C | T | 1 | a0001c0014 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1071C>T | p.His357His | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/13 | 1194/2207 | 1071/1869 | 357/622 | chr6 | 87428736 | |||
| chr6:87461126 | G | A | 1 | a0001c0008 | 2 | NA19043.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1599G>A | p.Glu533Glu | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/13 | 1722/2207 | 1599/1869 | 533/622 | chr6 | 87461126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87408021 | C | G | 1 | a0001c0001t0004 | 4 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-74C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/13 | 1819 | chr6 | 87408021 | ||||||
| chr6:87408060 | A | G | 1 | a0001c0001t0003 | 9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-35A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/13 | 1780 | chr6 | 87408060 | ||||||
| chr6:87408061 | C | A | 1 | a0001c0001t0003 | 9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-34C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/13 | 1779 | chr6 | 87408061 | ||||||
| chr6:87464384 | C | G | 8 | a0001c0001t0002 a0001c0008t0002 a0001c0014t0002 others(5): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*134C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 13/13 | 134 | chr6 | 87464384 | ||||||
| chr6:87464396 | C | A | 8 | a0001c0001t0002 a0001c0008t0002 a0001c0014t0002 others(5): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 13/13 | 146 | chr6 | 87464396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87408100 | T | G | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6+11T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408100 | |||||||
| chr6:87408229 | T | C | 1 | a0001c0008t0002g0026 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-6+140T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408229 | |||||||
| chr6:87408238 | C | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0325 others(15): Show |
20 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-6+149C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408238 | |||||||
| chr6:87408262 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+173C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408262 | |||||||
| chr6:87408346 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+257T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408346 | |||||||
| chr6:87408363 | C | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+274C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408363 | |||||||
| chr6:87408443 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+354C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408443 | |||||||
| chr6:87408455 | T | TGCGCACA others(12): Show |
33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0185 others(30): Show |
37 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-6+503_-6+521dupCA others(17): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(31): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0203 others(21): Show |
30 | HG00438.hp2 HG00558.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-6+484_-6+521dupCA others(36): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(50): Show |
8 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(5): Show |
8 | HG01884.hp1 HG02486.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+465_-6+521dupCA others(55): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(69): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0329 others(4): Show |
9 | HG02109.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6+446_-6+521dupCA others(74): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(88): Show |
8 | a0001c0001t0001g0229 a0001c0001t0001g0335 a0001c0001t0001g0336 others(5): Show |
8 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6+427_-6+521dupCA others(93): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(107): Show |
2 | a0001c0001t0004g0018 a0001c0001t0004g0230 |
3 | HG02615.hp1 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6+408_-6+521dupCA others(112): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | T | TGCGCACA others(126): Show |
1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6+389_-6+521dupCA others(131): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | TGCGCACA others(12): Show |
T | 62 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0087 others(59): Show |
70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-6+503_-6+521delCA others(17): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | TGCGCACA others(31): Show |
T | 3 | a0001c0001t0001g0324 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | HG03225.hp1 NA18906.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-6+484_-6+521delCA others(36): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | TGCGCACA others(50): Show |
T | 1 | a0001c0001t0001g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+465_-6+521delCA others(55): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408455 | TGCGCACA others(126): Show |
T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+389_-6+521del | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408455 | ||||||
| chr6:87408543 | T | TCCGGAGC others(31): Show |
1 | a0001c0001t0001g0136 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-6+491_-6+492insCC others(36): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408543 | ||||||
| chr6:87408672 | A | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+583A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408672 | |||||||
| chr6:87408676 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-6+587G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408676 | |||||||
| chr6:87408726 | C | CAT | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+638_-6+639insTA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87408726 | ||||||
| chr6:87408798 | G | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(7): Show |
15 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-6+709G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408798 | |||||||
| chr6:87408891 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+802A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408891 | |||||||
| chr6:87408931 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-6+842A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87408931 | |||||||
| chr6:87409023 | T | TTTATG | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-810_-5-809insAT others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87409023 | ||||||
| chr6:87409119 | C | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-716C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409119 | |||||||
| chr6:87409120 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-715T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409120 | |||||||
| chr6:87409227 | C | CT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
111 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5-595dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87409227 | ||||||
| chr6:87409241 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-594C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409241 | |||||||
| chr6:87409283 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
105 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.-5-552A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409283 | |||||||
| chr6:87409295 | C | A | 99 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(96): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5-540C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409295 | |||||||
| chr6:87409307 | G | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-528G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409307 | |||||||
| chr6:87409358 | C | T | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5-477C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409358 | |||||||
| chr6:87409375 | G | A | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-5-460G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409375 | |||||||
| chr6:87409397 | G | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5-438G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409397 | |||||||
| chr6:87409521 | CT | C | 114 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0058 others(111): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-5-299delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87409521 | ||||||
| chr6:87409536 | T | A | 40 | a0001c0008t0002g0026 a0001c0008t0002g0247 a0002c0002t0001g0021 others(37): Show |
42 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-5-299T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409536 | |||||||
| chr6:87409536 | T | TA | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
63 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5-297dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87409536 | ||||||
| chr6:87409536 | T | TTA | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5-299_-5-298insTA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409536 | |||||||
| chr6:87409810 | TA | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
114 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.-5-17delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 87409810 | ||||||
| chr6:87409811 | A | T | 3 | a0001c0001t0002g0067 a0001c0001t0004g0018 a0001c0001t0004g0230 |
4 | HG02615.hp1 HG02622.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-24A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409811 | |||||||
| chr6:87409812 | A | T | 1 | a0002c0002t0001g0283 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5-23A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 1/12 | chr6 | 87409812 | |||||||
| chr6:87409975 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.108+28G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87409975 | |||||||
| chr6:87410018 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.108+71T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410018 | |||||||
| chr6:87410065 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0230 a0001c0001t0004g0231 |
4 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+118C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410065 | |||||||
| chr6:87410179 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.108+232G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410179 | |||||||
| chr6:87410194 | A | T | 1 | a0001c0001t0001g0323 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.108+247A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410194 | |||||||
| chr6:87410262 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.108+315G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410262 | |||||||
| chr6:87410303 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.109-282G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410303 | |||||||
| chr6:87410389 | T | C | 1 | a0002c0002t0001g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109-196T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410389 | |||||||
| chr6:87410416 | A | T | 1 | a0002c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.109-169A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 2/12 | chr6 | 87410416 | |||||||
| chr6:87410698 | A | G | 24 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0241 others(21): Show |
26 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+30A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87410698 | |||||||
| chr6:87410794 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.192+126A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87410794 | |||||||
| chr6:87410940 | C | A | 1 | a0001c0001t0001g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+272C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87410940 | |||||||
| chr6:87411060 | AT | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.192+395delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 87411060 | ||||||
| chr6:87411123 | T | C | 4 | a0003c0004t0001g0020 a0003c0004t0001g0243 a0003c0004t0001g0244 others(1): Show |
5 | HG00741.hp1 HG01358.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+455T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411123 | |||||||
| chr6:87411202 | G | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
105 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.192+534G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411202 | |||||||
| chr6:87411225 | AGTTC | A | 3 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 |
3 | HG01358.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192+560_192+563del others(4): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 87411225 | ||||||
| chr6:87411229 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
110 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.192+561C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411229 | |||||||
| chr6:87411276 | C | G | 38 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0241 others(35): Show |
40 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.192+608C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411276 | |||||||
| chr6:87411318 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.192+650C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411318 | |||||||
| chr6:87411501 | A | G | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+833A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411501 | |||||||
| chr6:87411505 | ATT | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
113 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.192+840_192+841del others(2): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 87411505 | ||||||
| chr6:87411575 | G | A | 95 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(92): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.192+907G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411575 | |||||||
| chr6:87411615 | GT | G | 5 | a0001c0001t0002g0010 a0001c0001t0002g0030 a0001c0001t0002g0088 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+954delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 87411615 | ||||||
| chr6:87411962 | G | A | 4 | a0002c0002t0001g0249 a0002c0002t0001g0264 a0002c0002t0001g0265 others(1): Show |
4 | HG00280.hp1 HG00639.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1294G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87411962 | |||||||
| chr6:87412214 | G | C | 14 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0001g0285 others(11): Show |
14 | HG00597.hp2 NA18945.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+1546G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412214 | |||||||
| chr6:87412215 | C | A | 14 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0001g0285 others(11): Show |
14 | HG00597.hp2 NA18945.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+1547C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412215 | |||||||
| chr6:87412302 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-1508A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412302 | |||||||
| chr6:87412340 | A | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01943.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.193-1470A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412340 | |||||||
| chr6:87412373 | A | C | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193-1437A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412373 | |||||||
| chr6:87412512 | A | C | 3 | a0001c0001t0004g0018 a0001c0001t0004g0230 a0001c0001t0004g0231 |
4 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-1298A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412512 | |||||||
| chr6:87412713 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0230 a0001c0001t0004g0231 |
4 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-1097C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412713 | |||||||
| chr6:87412886 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0328 others(11): Show |
16 | HG02109.hp2 HG02615.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.193-924C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412886 | |||||||
| chr6:87412963 | C | T | 1 | a0001c0003t0001g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.193-847C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87412963 | |||||||
| chr6:87413024 | A | G | 1 | a0012c0017t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.193-786A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413024 | |||||||
| chr6:87413035 | G | GT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(14): Show |
19 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.193-771dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 87413035 | ||||||
| chr6:87413065 | C | T | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193-745C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413065 | |||||||
| chr6:87413161 | A | G | 7 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(4): Show |
7 | HG01081.hp1 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-649A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413161 | |||||||
| chr6:87413286 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
135 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.193-524T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413286 | |||||||
| chr6:87413329 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.193-481A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413329 | |||||||
| chr6:87413455 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.193-355T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413455 | |||||||
| chr6:87413567 | G | A | 1 | a0005c0006t0002g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.193-243G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413567 | |||||||
| chr6:87413676 | A | T | 1 | a0001c0001t0002g0080 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.193-134A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413676 | |||||||
| chr6:87413685 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.193-125G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413685 | |||||||
| chr6:87413741 | T | G | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193-69T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 3/12 | chr6 | 87413741 | |||||||
| chr6:87414009 | T | C | 2 | a0002c0002t0001g0253 a0002c0002t0001g0254 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283+109T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414009 | |||||||
| chr6:87414043 | C | CAAT | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.283+143_283+144ins others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414043 | |||||||
| chr6:87414262 | T | G | 1 | a0001c0001t0002g0089 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283+362T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414262 | |||||||
| chr6:87414495 | A | G | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+595A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414495 | |||||||
| chr6:87414665 | A | C | 1 | a0004c0005t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283+765A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414665 | |||||||
| chr6:87414673 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283+773A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414673 | |||||||
| chr6:87414760 | A | G | 3 | a0001c0001t0004g0018 a0001c0001t0004g0230 a0001c0001t0004g0231 |
4 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+860A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414760 | |||||||
| chr6:87414773 | G | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+873G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414773 | |||||||
| chr6:87414799 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.284-887C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414799 | |||||||
| chr6:87414820 | T | G | 2 | a0001c0001t0001g0326 a0011c0016t0001g0327 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.284-866T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414820 | |||||||
| chr6:87414966 | G | C | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.284-720G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414966 | |||||||
| chr6:87414980 | G | T | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-706G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87414980 | |||||||
| chr6:87415142 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.284-544G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415142 | |||||||
| chr6:87415153 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-533G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415153 | |||||||
| chr6:87415209 | C | T | 1 | a0002c0002t0001g0281 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.284-477C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415209 | |||||||
| chr6:87415312 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-374G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415312 | |||||||
| chr6:87415506 | C | T | 3 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 |
3 | HG02257.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.284-180C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415506 | |||||||
| chr6:87415527 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01192.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.284-159A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415527 | |||||||
| chr6:87415528 | C | T | 1 | a0003c0004t0001g0020 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-158C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415528 | |||||||
| chr6:87415529 | A | G | 8 | a0001c0001t0001g0173 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-157A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 4/12 | chr6 | 87415529 | |||||||
| chr6:87415953 | G | C | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.472+79G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87415953 | |||||||
| chr6:87415983 | G | GA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0297 others(4): Show |
8 | HG01433.hp2 HG03492.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+124dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 87415983 | ||||||
| chr6:87415983 | GA | G | 26 | a0001c0001t0001g0315 a0001c0001t0001g0324 a0001c0001t0001g0326 others(23): Show |
29 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.472+124delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 87415983 | ||||||
| chr6:87415983 | GAAA | G | 6 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(3): Show |
6 | HG01358.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+122_472+124del others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 87415983 | ||||||
| chr6:87416092 | T | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.472+218T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416092 | |||||||
| chr6:87416205 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.472+331A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416205 | |||||||
| chr6:87416240 | T | C | 1 | a0002c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.472+366T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416240 | |||||||
| chr6:87416413 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.473-256A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416413 | |||||||
| chr6:87416416 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.473-253C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416416 | |||||||
| chr6:87416449 | T | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.473-220T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 5/12 | chr6 | 87416449 | |||||||
| chr6:87417056 | A | G | 1 | a0012c0017t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.631+229A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417056 | |||||||
| chr6:87417205 | A | G | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | NA18953.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.631+378A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417205 | |||||||
| chr6:87417239 | A | G | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+412A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417239 | |||||||
| chr6:87417312 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.631+485G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417312 | |||||||
| chr6:87417383 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(35): Show |
46 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.631+556G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417383 | |||||||
| chr6:87417553 | C | CT | 37 | a0001c0003t0001g0172 a0001c0014t0002g0025 a0002c0002t0001g0021 others(34): Show |
39 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.632-639dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 87417553 | ||||||
| chr6:87417755 | C | CT | 82 | a0001c0001t0001g0007 a0001c0001t0001g0164 a0001c0001t0001g0218 others(79): Show |
88 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.632-436dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 87417755 | ||||||
| chr6:87417755 | C | CTT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
68 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.632-437_632-436dup others(2): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 87417755 | ||||||
| chr6:87417776 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.632-432A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417776 | |||||||
| chr6:87417817 | G | A | 2 | a0001c0001t0002g0091 a0001c0001t0002g0176 |
2 | NA19000.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.632-391G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417817 | |||||||
| chr6:87417889 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.632-319G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417889 | |||||||
| chr6:87417985 | G | A | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.632-223G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87417985 | |||||||
| chr6:87418085 | T | A | 1 | a0001c0001t0002g0035 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.632-123T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87418085 | |||||||
| chr6:87418087 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.632-121C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87418087 | |||||||
| chr6:87418101 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-107G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87418101 | |||||||
| chr6:87418103 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.632-105G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 6/12 | chr6 | 87418103 | |||||||
| chr6:87418549 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.840+133A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418549 | |||||||
| chr6:87418724 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.840+308T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418724 | |||||||
| chr6:87418806 | A | T | 3 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 |
3 | HG02257.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.840+390A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418806 | |||||||
| chr6:87418820 | G | GT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
63 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.840+410dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87418820 | ||||||
| chr6:87418887 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.840+471A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418887 | |||||||
| chr6:87418900 | C | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+484C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418900 | |||||||
| chr6:87418968 | C | T | 2 | a0001c0001t0001g0162 a0001c0007t0001g0240 |
2 | HG02257.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.840+552C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418968 | |||||||
| chr6:87418999 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(14): Show |
19 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.840+583C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87418999 | |||||||
| chr6:87419080 | C | CTGGCATG others(2): Show |
117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
131 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.840+666_840+667ins others(9): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87419080 | ||||||
| chr6:87419118 | TTTG | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+705_840+707del others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87419118 | ||||||
| chr6:87419121 | G | GT | 10 | a0001c0001t0001g0096 a0001c0001t0001g0143 a0001c0001t0002g0002 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.840+716dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87419121 | ||||||
| chr6:87419205 | A | G | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+789A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419205 | |||||||
| chr6:87419246 | A | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
131 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.840+830A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419246 | |||||||
| chr6:87419382 | A | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+966A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419382 | |||||||
| chr6:87419473 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.840+1057T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419473 | |||||||
| chr6:87419554 | C | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+1138C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419554 | |||||||
| chr6:87419596 | T | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.840+1180T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419596 | |||||||
| chr6:87419795 | C | G | 5 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+1379C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419795 | |||||||
| chr6:87419940 | G | A | 7 | a0001c0001t0003g0003 a0001c0001t0003g0083 a0001c0001t0003g0084 others(4): Show |
9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+1524G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419940 | |||||||
| chr6:87419948 | T | C | 2 | a0001c0003t0001g0121 a0001c0003t0001g0163 |
2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.840+1532T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87419948 | |||||||
| chr6:87420032 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+1616A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420032 | |||||||
| chr6:87420202 | A | C | 3 | a0004c0005t0001g0260 a0004c0005t0001g0261 a0004c0005t0001g0262 |
3 | HG01934.hp1 HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.840+1786A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420202 | |||||||
| chr6:87420223 | A | T | 3 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 |
3 | HG02257.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.840+1807A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420223 | |||||||
| chr6:87420372 | G | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.840+1956G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420372 | |||||||
| chr6:87420396 | T | A | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.840+1980T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420396 | |||||||
| chr6:87420505 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+2089G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420505 | |||||||
| chr6:87420607 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0298 a0001c0001t0001g0299 |
5 | HG02559.hp1 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+2191T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420607 | |||||||
| chr6:87420873 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.840+2457A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87420873 | |||||||
| chr6:87421084 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.840+2668A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421084 | |||||||
| chr6:87421314 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.840+2898C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421314 | |||||||
| chr6:87421343 | G | C | 3 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02922.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.840+2927G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421343 | |||||||
| chr6:87421350 | G | T | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.840+2934G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421350 | |||||||
| chr6:87421434 | T | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+3018T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421434 | |||||||
| chr6:87421491 | G | GA | 9 | a0002c0002t0001g0021 a0002c0002t0001g0241 a0002c0002t0001g0267 others(6): Show |
10 | HG02056.hp1 HG02132.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.840+3085dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87421491 | ||||||
| chr6:87421503 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.840+3087C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421503 | |||||||
| chr6:87421671 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.840+3255G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421671 | |||||||
| chr6:87421895 | A | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.840+3479A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421895 | |||||||
| chr6:87421963 | G | A | 3 | a0004c0005t0001g0260 a0004c0005t0001g0261 a0004c0005t0001g0262 |
3 | HG01934.hp1 HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.840+3547G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87421963 | |||||||
| chr6:87422033 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.840+3617T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422033 | |||||||
| chr6:87422150 | A | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
103 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.840+3734A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422150 | |||||||
| chr6:87422157 | A | C | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.840+3741A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422157 | |||||||
| chr6:87422171 | G | A | 4 | a0003c0004t0001g0020 a0003c0004t0001g0243 a0003c0004t0001g0244 others(1): Show |
5 | HG00741.hp1 HG01358.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+3755G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422171 | |||||||
| chr6:87422203 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.840+3787C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422203 | |||||||
| chr6:87422343 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0090 |
2 | HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.840+3927G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422343 | |||||||
| chr6:87422392 | A | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
131 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.840+3976A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422392 | |||||||
| chr6:87422399 | A | G | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+3983A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422399 | |||||||
| chr6:87422451 | G | GA | 37 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(34): Show |
37 | HG00438.hp1 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.840+4053dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87422451 | ||||||
| chr6:87422451 | GA | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0161 a0001c0001t0001g0314 others(15): Show |
20 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.840+4053delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87422451 | ||||||
| chr6:87422479 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0002g0334 |
5 | HG02109.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-4047C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422479 | |||||||
| chr6:87422480 | G | A | 2 | a0001c0007t0001g0239 a0001c0007t0001g0240 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.841-4046G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422480 | |||||||
| chr6:87422485 | CTCACGCC others(5): Show |
C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0002g0334 |
5 | HG02109.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-4038_841-4027d others(14): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87422485 | ||||||
| chr6:87422608 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.841-3918C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422608 | |||||||
| chr6:87422652 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.841-3874G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422652 | |||||||
| chr6:87422750 | C | CA | 22 | a0001c0001t0001g0007 a0001c0001t0001g0131 a0001c0001t0001g0204 others(19): Show |
24 | HG02040.hp2 HG02109.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.841-3763dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87422750 | ||||||
| chr6:87422750 | CA | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-3763delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87422750 | ||||||
| chr6:87422759 | A | AC | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
102 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.841-3767_841-3766i others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422759 | |||||||
| chr6:87422759 | A | C | 1 | a0001c0001t0001g0232 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.841-3767A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422759 | |||||||
| chr6:87422760 | A | AC | 3 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02922.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.841-3766_841-3765i others(3): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422760 | |||||||
| chr6:87422774 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0001g0135 a0001c0001t0001g0160 others(2): Show |
5 | HG00323.hp1 HG01433.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-3752A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422774 | |||||||
| chr6:87422830 | G | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-3696G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422830 | |||||||
| chr6:87422953 | C | T | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.841-3573C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422953 | |||||||
| chr6:87422992 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.841-3534G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87422992 | |||||||
| chr6:87423123 | T | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.841-3403T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423123 | |||||||
| chr6:87423240 | AT | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.841-3279delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87423240 | ||||||
| chr6:87423349 | C | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-3177C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423349 | |||||||
| chr6:87423381 | T | A | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-3145T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423381 | |||||||
| chr6:87423396 | C | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
105 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.841-3130C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423396 | |||||||
| chr6:87423404 | A | G | 2 | a0002c0002t0001g0241 a0002c0002t0001g0272 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.841-3122A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423404 | |||||||
| chr6:87423407 | T | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-3119T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423407 | |||||||
| chr6:87423427 | C | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.841-3099C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423427 | |||||||
| chr6:87423435 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
6 | HG01175.hp2 HG01257.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-3091A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423435 | |||||||
| chr6:87423519 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.841-3007G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423519 | |||||||
| chr6:87423554 | T | A | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.841-2972T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423554 | |||||||
| chr6:87423597 | G | A | 235 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.841-2929G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423597 | |||||||
| chr6:87423622 | G | A | 1 | a0002c0002t0001g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.841-2904G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423622 | |||||||
| chr6:87423741 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.841-2785T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423741 | |||||||
| chr6:87423785 | A | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
105 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.841-2741A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423785 | |||||||
| chr6:87423799 | CAGG | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-2718_841-2716d others(5): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 87423799 | ||||||
| chr6:87423854 | G | T | 1 | a0001c0001t0002g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.841-2672G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423854 | |||||||
| chr6:87423867 | AT | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0324 a0001c0001t0001g0326 others(13): Show |
18 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.841-2658delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423867 | |||||||
| chr6:87423947 | T | C | 1 | a0003c0004t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.841-2579T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87423947 | |||||||
| chr6:87424036 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.841-2490A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424036 | |||||||
| chr6:87424149 | C | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-2377C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424149 | |||||||
| chr6:87424299 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-2227G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424299 | |||||||
| chr6:87424311 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.841-2215G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424311 | |||||||
| chr6:87424697 | G | A | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.841-1829G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424697 | |||||||
| chr6:87424788 | T | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0218 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.841-1738T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424788 | |||||||
| chr6:87424793 | T | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.841-1733T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424793 | |||||||
| chr6:87424927 | A | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.841-1599A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424927 | |||||||
| chr6:87424987 | A | G | 2 | a0001c0007t0001g0239 a0001c0007t0001g0240 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.841-1539A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87424987 | |||||||
| chr6:87425008 | C | T | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.841-1518C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425008 | |||||||
| chr6:87425238 | A | C | 4 | a0003c0004t0001g0020 a0003c0004t0001g0243 a0003c0004t0001g0244 others(1): Show |
5 | HG00741.hp1 HG01358.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-1288A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425238 | |||||||
| chr6:87425265 | C | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-1261C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425265 | |||||||
| chr6:87425513 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-1013G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425513 | |||||||
| chr6:87425763 | C | T | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.841-763C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425763 | |||||||
| chr6:87425990 | A | G | 101 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(98): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.841-536A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87425990 | |||||||
| chr6:87426102 | G | A | 10 | a0001c0001t0002g0036 a0001c0001t0002g0043 a0001c0001t0002g0044 others(7): Show |
10 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.841-424G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87426102 | |||||||
| chr6:87426210 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0110 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.841-316A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87426210 | |||||||
| chr6:87426225 | C | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-301C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87426225 | |||||||
| chr6:87426306 | C | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-220C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87426306 | |||||||
| chr6:87426439 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0218 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.841-87A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 7/12 | chr6 | 87426439 | |||||||
| chr6:87426792 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+147G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87426792 | |||||||
| chr6:87426836 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+191G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87426836 | |||||||
| chr6:87426852 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.960+207G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87426852 | |||||||
| chr6:87427207 | G | A | 1 | a0002c0002t0001g0274 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.960+562G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427207 | |||||||
| chr6:87427251 | G | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+606G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427251 | |||||||
| chr6:87427374 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.960+729C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427374 | |||||||
| chr6:87427383 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0160 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.960+738C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427383 | |||||||
| chr6:87427430 | C | T | 21 | a0001c0003t0001g0016 a0001c0003t0001g0119 a0001c0003t0001g0121 others(18): Show |
22 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.960+785C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427430 | |||||||
| chr6:87427511 | A | C | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.960+866A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427511 | |||||||
| chr6:87427549 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.960+904G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427549 | |||||||
| chr6:87427727 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.961-899G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427727 | |||||||
| chr6:87427790 | T | C | 5 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-836T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427790 | |||||||
| chr6:87427841 | T | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0208 |
2 | NA19058.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.961-785T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87427841 | |||||||
| chr6:87427982 | C | CT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
106 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.961-622dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 87427982 | ||||||
| chr6:87427982 | C | CTT | 7 | a0001c0001t0001g0159 a0001c0014t0002g0025 a0002c0002t0001g0267 others(4): Show |
7 | HG00642.hp1 HG02145.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-623_961-622dup others(2): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 87427982 | ||||||
| chr6:87427982 | CT | C | 11 | a0001c0001t0001g0096 a0001c0001t0001g0335 a0001c0001t0002g0051 others(8): Show |
11 | HG00280.hp2 HG01516.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.961-622delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 87427982 | ||||||
| chr6:87427982 | CTT | C | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-623_961-622del others(2): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 87427982 | ||||||
| chr6:87428145 | G | A | 1 | a0002c0002t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.961-481G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428145 | |||||||
| chr6:87428214 | C | G | 1 | a0004c0005t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.961-412C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428214 | |||||||
| chr6:87428217 | C | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.961-409C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428217 | |||||||
| chr6:87428265 | G | A | 2 | a0001c0001t0001g0326 a0011c0016t0001g0327 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.961-361G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428265 | |||||||
| chr6:87428287 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.961-339C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428287 | |||||||
| chr6:87428290 | AT | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
105 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.961-323delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 87428290 | ||||||
| chr6:87428384 | A | G | 36 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0241 others(33): Show |
38 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.961-242A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428384 | |||||||
| chr6:87428409 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-217G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428409 | |||||||
| chr6:87428423 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.961-203T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 8/12 | chr6 | 87428423 | |||||||
| chr6:87428886 | C | T | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1159+62C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87428886 | |||||||
| chr6:87428962 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1159+138C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87428962 | |||||||
| chr6:87429019 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1159+195T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429019 | |||||||
| chr6:87429038 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | NA18954.hp2 NA18985.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+214C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429038 | |||||||
| chr6:87429220 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1159+396C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429220 | |||||||
| chr6:87429232 | G | GA | 14 | a0001c0001t0001g0133 a0001c0001t0001g0210 a0001c0001t0001g0287 others(11): Show |
15 | HG00741.hp1 HG01358.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1159+423dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 87429232 | ||||||
| chr6:87429498 | T | C | 1 | a0001c0007t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1159+674T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429498 | |||||||
| chr6:87429507 | A | T | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+683A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429507 | |||||||
| chr6:87429584 | T | G | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+760T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429584 | |||||||
| chr6:87429636 | C | A | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1159+812C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429636 | |||||||
| chr6:87429656 | T | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.1159+832T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429656 | |||||||
| chr6:87429830 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1159+1006A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429830 | |||||||
| chr6:87429838 | T | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.1159+1014T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429838 | |||||||
| chr6:87429900 | G | A | 7 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 others(4): Show |
8 | HG00741.hp1 HG01358.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1076G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87429900 | |||||||
| chr6:87429929 | GTAAGCAA others(3): Show |
G | 2 | a0002c0002t0001g0259 a0002c0002t0002g0257 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1160-1102_1160-109 others(14): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 87429929 | ||||||
| chr6:87430019 | C | A | 1 | a0001c0001t0002g0053 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1160-1014C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430019 | |||||||
| chr6:87430026 | G | T | 1 | a0001c0003t0001g0172 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1160-1007G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430026 | |||||||
| chr6:87430157 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1160-876G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430157 | |||||||
| chr6:87430160 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01192.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1160-873A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430160 | |||||||
| chr6:87430327 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1160-706A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430327 | |||||||
| chr6:87430515 | G | T | 2 | a0002c0002t0001g0274 a0002c0002t0001g0279 |
2 | HG04204.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1160-518G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430515 | |||||||
| chr6:87430825 | G | A | 3 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02922.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1160-208G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430825 | |||||||
| chr6:87430903 | C | A | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-130C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430903 | |||||||
| chr6:87430914 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0158 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1160-119C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430914 | |||||||
| chr6:87430925 | A | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1160-108A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430925 | |||||||
| chr6:87430966 | G | A | 2 | a0001c0001t0001g0326 a0011c0016t0001g0327 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1160-67G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430966 | |||||||
| chr6:87430993 | C | A | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1160-40C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 9/12 | chr6 | 87430993 | |||||||
| chr6:87431266 | T | A | 2 | a0007c0011t0001g0228 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1300+93T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431266 | |||||||
| chr6:87431296 | G | T | 3 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 |
3 | HG01358.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1300+123G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431296 | |||||||
| chr6:87431346 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
106 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1300+173A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431346 | |||||||
| chr6:87431377 | T | G | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1300+204T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431377 | |||||||
| chr6:87431403 | T | C | 2 | a0001c0007t0001g0239 a0001c0007t0001g0240 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1300+230T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431403 | |||||||
| chr6:87431439 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0235 a0001c0001t0001g0236 |
5 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+266G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431439 | |||||||
| chr6:87431503 | C | T | 3 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 |
3 | HG02257.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1300+330C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431503 | |||||||
| chr6:87431690 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+517C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431690 | |||||||
| chr6:87431909 | TTC | T | 9 | a0001c0003t0001g0016 a0001c0003t0001g0194 a0001c0003t0001g0197 others(6): Show |
10 | HG00423.hp1 HG00558.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1300+740_1300+741d others(4): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87431909 | ||||||
| chr6:87431921 | C | T | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+748C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431921 | |||||||
| chr6:87431940 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1300+767A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87431940 | |||||||
| chr6:87432056 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1300+883G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432056 | |||||||
| chr6:87432072 | G | A | 3 | a0001c0007t0001g0239 a0001c0007t0001g0240 a0001c0007t0001g0246 |
3 | HG02257.hp1 HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1300+899G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432072 | |||||||
| chr6:87432244 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1300+1071G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432244 | |||||||
| chr6:87432274 | A | G | 1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1300+1101A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432274 | |||||||
| chr6:87432339 | C | CTGAGGCC others(3): Show |
1 | a0001c0001t0002g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1300+1172_1300+118 others(14): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87432339 | ||||||
| chr6:87432373 | A | C | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+1200A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432373 | |||||||
| chr6:87432470 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1300+1297C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432470 | |||||||
| chr6:87432556 | CA | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1300+1385delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87432556 | ||||||
| chr6:87432656 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1300+1483G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432656 | |||||||
| chr6:87432751 | G | A | 1 | a0001c0003t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1300+1578G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432751 | |||||||
| chr6:87432856 | T | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0088 |
3 | HG01070.hp2 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1300+1683T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432856 | |||||||
| chr6:87432967 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0328 a0001c0001t0001g0329 others(7): Show |
12 | HG02109.hp2 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1300+1794A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87432967 | |||||||
| chr6:87433047 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1301-1813T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433047 | |||||||
| chr6:87433256 | A | G | 5 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0001c0001t0001g0330 others(2): Show |
5 | HG02486.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1301-1604A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433256 | |||||||
| chr6:87433261 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
104 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1301-1599A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433261 | |||||||
| chr6:87433318 | T | G | 4 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-1542T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433318 | |||||||
| chr6:87433633 | C | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1301-1227C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433633 | |||||||
| chr6:87433697 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1301-1163A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433697 | |||||||
| chr6:87433700 | T | G | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1301-1160T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433700 | |||||||
| chr6:87433916 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1301-944T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433916 | |||||||
| chr6:87433929 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1301-931G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433929 | |||||||
| chr6:87433952 | T | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1301-908T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87433952 | |||||||
| chr6:87434099 | C | CA | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
115 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1301-751dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434099 | ||||||
| chr6:87434350 | T | G | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1301-510T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87434350 | |||||||
| chr6:87434418 | C | CA | 10 | a0001c0001t0001g0136 a0001c0001t0001g0188 a0001c0001t0001g0286 others(7): Show |
10 | HG02486.hp2 HG02922.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1301-427dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434418 | ||||||
| chr6:87434418 | CA | C | 108 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(105): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1301-427delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434418 | ||||||
| chr6:87434502 | C | CT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
87 | HG00280.hp1 HG00597.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1301-343dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434502 | ||||||
| chr6:87434502 | CT | C | 112 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(109): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1301-343delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434502 | ||||||
| chr6:87434686 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
104 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1301-174C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | chr6 | 87434686 | |||||||
| chr6:87434757 | C | CAAAGTGC others(12): Show |
1 | a0001c0003t0001g0221 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1301-102_1301-84du others(20): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 87434757 | ||||||
| chr6:87435402 | C | T | 4 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+349C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435402 | |||||||
| chr6:87435585 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1494+532C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435585 | |||||||
| chr6:87435620 | A | C | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+567A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435620 | |||||||
| chr6:87435630 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1494+577C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435630 | |||||||
| chr6:87435834 | A | T | 1 | a0001c0003t0001g0221 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1494+781A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435834 | |||||||
| chr6:87435857 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1494+804G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87435857 | |||||||
| chr6:87436024 | T | C | 1 | a0001c0003t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1494+971T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436024 | |||||||
| chr6:87436084 | C | CT | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
58 | HG00280.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1494+1052dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87436084 | ||||||
| chr6:87436084 | CT | C | 12 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0311 others(9): Show |
12 | HG00544.hp2 HG01167.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1494+1052delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87436084 | ||||||
| chr6:87436084 | CTT | C | 99 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(96): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1494+1051_1494+105 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87436084 | ||||||
| chr6:87436247 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1494+1194G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436247 | |||||||
| chr6:87436352 | C | T | 1 | a0001c0001t0004g0231 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1494+1299C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436352 | |||||||
| chr6:87436365 | C | T | 2 | a0001c0014t0002g0025 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1494+1312C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436365 | |||||||
| chr6:87436534 | A | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(333): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1494+1481A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436534 | |||||||
| chr6:87436677 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1494+1624G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436677 | |||||||
| chr6:87436883 | T | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+1830T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436883 | |||||||
| chr6:87436911 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1494+1858G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436911 | |||||||
| chr6:87436964 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1494+1911C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87436964 | |||||||
| chr6:87437101 | C | G | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | NA18953.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1494+2048C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437101 | |||||||
| chr6:87437102 | T | G | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | NA18953.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1494+2049T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437102 | |||||||
| chr6:87437363 | T | A | 1 | a0002c0002t0001g0269 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1494+2310T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437363 | |||||||
| chr6:87437376 | G | GT | 115 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(112): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1494+2332dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87437376 | ||||||
| chr6:87437377 | T | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+2324T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437377 | |||||||
| chr6:87437488 | C | G | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+2435C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437488 | |||||||
| chr6:87437493 | C | A | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+2440C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437493 | |||||||
| chr6:87437546 | T | C | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+2493T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437546 | |||||||
| chr6:87437596 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1494+2543T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437596 | |||||||
| chr6:87437825 | A | AT | 69 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0123 others(66): Show |
72 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1494+2798dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87437825 | ||||||
| chr6:87437825 | A | ATT | 12 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0148 others(9): Show |
12 | HG00408.hp1 HG01175.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1494+2797_1494+279 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87437825 | ||||||
| chr6:87437825 | AT | A | 19 | a0001c0001t0001g0124 a0001c0001t0001g0152 a0001c0001t0001g0284 others(16): Show |
19 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1494+2798delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87437825 | ||||||
| chr6:87437859 | G | A | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+2806G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437859 | |||||||
| chr6:87437861 | T | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+2808T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437861 | |||||||
| chr6:87437872 | C | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0133 others(4): Show |
7 | HG00733.hp2 HG00735.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1494+2819C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87437872 | |||||||
| chr6:87438084 | A | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
104 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1494+3031A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438084 | |||||||
| chr6:87438258 | C | T | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+3205C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438258 | |||||||
| chr6:87438294 | C | G | 1 | a0002c0002t0001g0277 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1494+3241C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438294 | |||||||
| chr6:87438457 | T | C | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+3404T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438457 | |||||||
| chr6:87438460 | C | CA | 26 | a0001c0001t0001g0118 a0001c0001t0001g0164 a0001c0001t0001g0187 others(23): Show |
29 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1494+3426dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87438460 | ||||||
| chr6:87438460 | C | CAA | 32 | a0001c0001t0001g0206 a0001c0001t0002g0049 a0002c0002t0001g0021 others(29): Show |
34 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1494+3425_1494+342 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87438460 | ||||||
| chr6:87438460 | C | CAAA | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1494+3424_1494+342 others(7): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87438460 | ||||||
| chr6:87438460 | C | CAAAA | 21 | a0001c0001t0001g0054 a0001c0001t0001g0235 a0001c0001t0001g0242 others(18): Show |
21 | HG00544.hp1 HG00642.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1494+3423_1494+342 others(8): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87438460 | ||||||
| chr6:87438605 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1494+3552T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438605 | |||||||
| chr6:87438649 | C | T | 4 | a0001c0003t0001g0165 a0001c0003t0001g0167 a0001c0003t0001g0170 others(1): Show |
4 | NA18963.hp2 NA18966.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+3596C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438649 | |||||||
| chr6:87438699 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1494+3646C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438699 | |||||||
| chr6:87438723 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1494+3670C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438723 | |||||||
| chr6:87438860 | G | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+3807G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87438860 | |||||||
| chr6:87439065 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1494+4012A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439065 | |||||||
| chr6:87439140 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1494+4087G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439140 | |||||||
| chr6:87439177 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1494+4124A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439177 | |||||||
| chr6:87439215 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0302 a0001c0001t0001g0304 others(3): Show |
6 | HG00733.hp1 HG00741.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1494+4162C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439215 | |||||||
| chr6:87439451 | A | AT | 15 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0001g0285 others(12): Show |
15 | HG00597.hp2 NA18945.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.1494+4402dupT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87439451 | ||||||
| chr6:87439458 | T | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1494+4405T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439458 | |||||||
| chr6:87439504 | G | T | 1 | a0001c0003t0001g0197 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1494+4451G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439504 | |||||||
| chr6:87439691 | A | G | 5 | a0001c0001t0001g0297 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
5 | HG00323.hp2 HG01256.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+4638A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439691 | |||||||
| chr6:87439879 | T | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+4826T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439879 | |||||||
| chr6:87439880 | A | T | 4 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+4827A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87439880 | |||||||
| chr6:87440105 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1494+5052A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87440105 | |||||||
| chr6:87440206 | T | G | 1 | a0001c0003t0001g0223 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1494+5153T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87440206 | |||||||
| chr6:87440237 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1494+5184C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87440237 | |||||||
| chr6:87440465 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1494+5412C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87440465 | |||||||
| chr6:87440531 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1494+5478T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87440531 | |||||||
| chr6:87441064 | A | G | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1494+6011A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441064 | |||||||
| chr6:87441093 | G | C | 1 | a0001c0003t0001g0221 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1494+6040G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441093 | |||||||
| chr6:87441098 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1494+6045A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441098 | |||||||
| chr6:87441123 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1494+6070C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441123 | |||||||
| chr6:87441366 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1494+6313A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441366 | |||||||
| chr6:87441413 | G | A | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1494+6360G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441413 | |||||||
| chr6:87441425 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0058 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1494+6372G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441425 | |||||||
| chr6:87441441 | G | A | 1 | a0003c0004t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1494+6388G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441441 | |||||||
| chr6:87441467 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1494+6414T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441467 | |||||||
| chr6:87441487 | C | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
62 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1494+6434C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441487 | |||||||
| chr6:87441521 | A | G | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+6468A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441521 | |||||||
| chr6:87441627 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1494+6574C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441627 | |||||||
| chr6:87441822 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1494+6769A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441822 | |||||||
| chr6:87441846 | C | T | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1494+6793C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441846 | |||||||
| chr6:87441949 | CT | C | 7 | a0001c0001t0003g0003 a0001c0001t0003g0083 a0001c0001t0003g0084 others(4): Show |
9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494+6897delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87441949 | |||||||
| chr6:87442148 | A | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0218 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1494+7095A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442148 | |||||||
| chr6:87442267 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1494+7214T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442267 | |||||||
| chr6:87442319 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1494+7266C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442319 | |||||||
| chr6:87442389 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1494+7336C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442389 | |||||||
| chr6:87442564 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1494+7511T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442564 | |||||||
| chr6:87442739 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1494+7686G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442739 | |||||||
| chr6:87442745 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1494+7692C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442745 | |||||||
| chr6:87442817 | C | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1494+7764C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442817 | |||||||
| chr6:87442924 | T | C | 102 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(99): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1494+7871T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442924 | |||||||
| chr6:87442949 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1494+7896G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442949 | |||||||
| chr6:87442955 | C | T | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1494+7902C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442955 | |||||||
| chr6:87442963 | A | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1494+7910A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442963 | |||||||
| chr6:87442972 | A | C | 1 | a0004c0005t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1494+7919A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87442972 | |||||||
| chr6:87443124 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1494+8071A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443124 | |||||||
| chr6:87443312 | C | G | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1494+8259C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443312 | |||||||
| chr6:87443336 | T | C | 3 | a0002c0002t0001g0253 a0002c0002t0001g0254 a0002c0002t0001g0259 |
3 | HG01884.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1494+8283T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443336 | |||||||
| chr6:87443481 | A | G | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+8428A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443481 | |||||||
| chr6:87443585 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0088 |
3 | HG01070.hp2 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1494+8532A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443585 | |||||||
| chr6:87443589 | TA | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(35): Show |
46 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1494+8537delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443589 | |||||||
| chr6:87443608 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1494+8555A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443608 | |||||||
| chr6:87443890 | C | T | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+8837C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443890 | |||||||
| chr6:87443975 | G | T | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+8922G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87443975 | |||||||
| chr6:87444213 | A | C | 1 | a0001c0001t0001g0309 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1494+9160A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444213 | |||||||
| chr6:87444265 | G | C | 206 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1494+9212G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444265 | |||||||
| chr6:87444387 | G | A | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1494+9334G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444387 | |||||||
| chr6:87444455 | T | G | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9402T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444455 | |||||||
| chr6:87444526 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1494+9473G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444526 | |||||||
| chr6:87444602 | A | G | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9549A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444602 | |||||||
| chr6:87444608 | A | T | 6 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0001c0001t0001g0330 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1494+9555A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444608 | |||||||
| chr6:87444619 | T | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9566T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444619 | |||||||
| chr6:87444715 | T | A | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1494+9662T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444715 | |||||||
| chr6:87444716 | C | A | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1494+9663C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444716 | |||||||
| chr6:87444879 | G | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9826G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444879 | |||||||
| chr6:87444896 | G | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9843G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444896 | |||||||
| chr6:87444962 | T | C | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+9909T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444962 | |||||||
| chr6:87444973 | A | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+9920A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87444973 | |||||||
| chr6:87445082 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0158 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1494+10029C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445082 | |||||||
| chr6:87445153 | G | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+10100G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445153 | |||||||
| chr6:87445427 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1494+10374G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445427 | |||||||
| chr6:87445438 | T | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0060 a0005c0006t0002g0032 others(3): Show |
7 | HG00408.hp2 NA18747.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1494+10385T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445438 | |||||||
| chr6:87445621 | A | G | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+10568A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445621 | |||||||
| chr6:87445781 | T | C | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+10728T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445781 | |||||||
| chr6:87445892 | C | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+10839C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445892 | |||||||
| chr6:87445951 | A | G | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+10898A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87445951 | |||||||
| chr6:87446162 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1494+11109C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446162 | |||||||
| chr6:87446186 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1494+11133C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446186 | |||||||
| chr6:87446235 | T | C | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1494+11182T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446235 | |||||||
| chr6:87446333 | A | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+11280A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446333 | |||||||
| chr6:87446388 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1494+11335T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446388 | |||||||
| chr6:87446596 | T | C | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1494+11543T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446596 | |||||||
| chr6:87446672 | A | G | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+11619A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446672 | |||||||
| chr6:87446682 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0058 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1494+11629T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446682 | |||||||
| chr6:87446814 | C | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+11761C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446814 | |||||||
| chr6:87446850 | G | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+11797G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446850 | |||||||
| chr6:87446898 | A | G | 2 | a0001c0001t0002g0091 a0001c0001t0002g0176 |
2 | NA19000.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1494+11845A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87446898 | |||||||
| chr6:87447002 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1494+11949C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447002 | |||||||
| chr6:87447163 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(35): Show |
46 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1494+12110A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447163 | |||||||
| chr6:87447178 | A | C | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+12125A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447178 | |||||||
| chr6:87447413 | G | A | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1494+12360G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447413 | |||||||
| chr6:87447464 | G | C | 102 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(99): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1494+12411G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447464 | |||||||
| chr6:87447582 | G | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+12529G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447582 | |||||||
| chr6:87447590 | T | C | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1494+12537T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447590 | |||||||
| chr6:87447669 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1494+12616G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447669 | |||||||
| chr6:87447674 | T | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1494+12621T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447674 | |||||||
| chr6:87447812 | C | A | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+12759C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447812 | |||||||
| chr6:87447890 | C | T | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1494+12837C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447890 | |||||||
| chr6:87447951 | T | TATATTAT others(8): Show |
1 | a0001c0001t0002g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1494+12898_1494+12 others(21): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447951 | |||||||
| chr6:87447951 | T | TTTATTAT others(5): Show |
20 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0043 others(17): Show |
21 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1494+12905_1494+12 others(18): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(8): Show |
8 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
8 | HG01081.hp1 HG01109.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1494+12902_1494+12 others(21): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(11): Show |
78 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(75): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1494+12899_1494+12 others(24): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(14): Show |
59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
69 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1494+12916_1494+12 others(27): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(17): Show |
16 | a0001c0001t0001g0233 a0001c0001t0001g0308 a0001c0001t0001g0332 others(13): Show |
17 | HG00741.hp2 HG01074.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1494+12916_1494+12 others(30): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(20): Show |
23 | a0001c0014t0002g0025 a0002c0002t0001g0022 a0002c0002t0001g0241 others(20): Show |
24 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+12916_1494+12 others(33): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447951 | T | TTTATTAT others(23): Show |
1 | a0002c0002t0001g0021 | 2 | NA18957.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1494+12916_1494+12 others(36): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447951 | ||||||
| chr6:87447970 | C | T | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1494+12917C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447970 | |||||||
| chr6:87447971 | T | TATTATTA others(11): Show |
1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1494+12920_1494+12 others(24): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87447971 | ||||||
| chr6:87447997 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1494+12944G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87447997 | |||||||
| chr6:87448004 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1494+12951G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448004 | |||||||
| chr6:87448237 | C | T | 1 | a0001c0003t0001g0196 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1495-12785C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448237 | |||||||
| chr6:87448845 | T | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0218 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1495-12177T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448845 | |||||||
| chr6:87448913 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1495-12109C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448913 | |||||||
| chr6:87448920 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0157 |
2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1495-12102G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448920 | |||||||
| chr6:87448968 | G | C | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12054G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448968 | |||||||
| chr6:87448972 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12050G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448972 | |||||||
| chr6:87448973 | C | CTACTCAC others(3): Show |
1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12049_1495-12 others(16): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448973 | |||||||
| chr6:87448977 | T | G | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12045T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448977 | |||||||
| chr6:87448985 | T | G | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12037T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448985 | |||||||
| chr6:87448992 | C | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-12030C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448992 | |||||||
| chr6:87448993 | T | G | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-12029T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448993 | |||||||
| chr6:87448994 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
104 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1495-12028A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448994 | |||||||
| chr6:87448996 | T | G | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12026T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87448996 | |||||||
| chr6:87449001 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12021T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449001 | |||||||
| chr6:87449017 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-12005G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449017 | |||||||
| chr6:87449031 | T | A | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-11991T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449031 | |||||||
| chr6:87449039 | T | A | 1 | a0001c0001t0002g0180 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1495-11983T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449039 | |||||||
| chr6:87449172 | C | T | 106 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(103): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1495-11850C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449172 | |||||||
| chr6:87449174 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1495-11848C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449174 | |||||||
| chr6:87449198 | A | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-11824A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449198 | |||||||
| chr6:87449369 | G | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-11653G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449369 | |||||||
| chr6:87449436 | C | CA | 19 | a0001c0001t0001g0058 a0001c0001t0001g0120 a0001c0001t0001g0131 others(16): Show |
19 | HG01884.hp1 HG02083.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1495-11561dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87449436 | ||||||
| chr6:87449436 | CA | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
98 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.1495-11561delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87449436 | ||||||
| chr6:87449436 | CAA | C | 12 | a0001c0001t0001g0237 a0001c0001t0001g0294 a0001c0001t0001g0315 others(9): Show |
13 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1495-11562_1495-11 others(8): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87449436 | ||||||
| chr6:87449439 | A | C | 23 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0241 others(20): Show |
25 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1495-11583A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449439 | |||||||
| chr6:87449440 | A | C | 11 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(8): Show |
11 | HG01358.hp1 HG01884.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495-11582A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449440 | |||||||
| chr6:87449558 | T | C | 206 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1495-11464T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449558 | |||||||
| chr6:87449612 | G | C | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-11410G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449612 | |||||||
| chr6:87449728 | A | C | 1 | a0001c0001t0002g0077 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1495-11294A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449728 | |||||||
| chr6:87449988 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1495-11034A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87449988 | |||||||
| chr6:87450152 | G | T | 2 | a0001c0001t0001g0118 a0009c0013t0001g0126 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1495-10870G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450152 | |||||||
| chr6:87450171 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1495-10851T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450171 | |||||||
| chr6:87450190 | C | A | 1 | a0012c0017t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1495-10832C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450190 | |||||||
| chr6:87450353 | G | A | 1 | a0001c0014t0002g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1495-10669G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450353 | |||||||
| chr6:87450475 | A | ATG | 21 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0001g0145 others(18): Show |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1495-10509_1495-10 others(8): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | A | ATGTG | 10 | a0001c0001t0001g0122 a0001c0001t0001g0204 a0001c0001t0001g0214 others(7): Show |
12 | HG00408.hp2 HG02055.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1495-10511_1495-10 others(10): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | A | ATGTGTG | 14 | a0001c0001t0002g0013 a0001c0001t0002g0030 a0001c0001t0002g0034 others(11): Show |
15 | HG00423.hp2 HG00597.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1495-10513_1495-10 others(12): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | A | ATGTGTGT others(1): Show |
59 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0002g0002 others(56): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1495-10515_1495-10 others(14): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | A | ATGTGTGT others(3): Show |
17 | a0001c0001t0001g0096 a0001c0001t0002g0039 a0001c0001t0002g0063 others(14): Show |
17 | HG01516.hp1 HG01952.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1495-10517_1495-10 others(16): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1495-10519_1495-10 others(18): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | ATG | A | 53 | a0001c0001t0001g0023 a0001c0001t0001g0226 a0001c0001t0001g0297 others(50): Show |
57 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1495-10509_1495-10 others(8): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | ATGTG | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
53 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1495-10511_1495-10 others(10): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | ATGTGTG | A | 10 | a0001c0001t0001g0305 a0001c0001t0001g0329 a0001c0001t0001g0335 others(7): Show |
10 | HG02165.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1495-10513_1495-10 others(12): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | ATGTGTGT others(1): Show |
A | 3 | a0001c0001t0001g0292 a0001c0001t0002g0057 a0001c0001t0002g0061 |
3 | HG00544.hp1 HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1495-10515_1495-10 others(14): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450475 | ATGTGTGT others(3): Show |
A | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-10517_1495-10 others(16): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450475 | ||||||
| chr6:87450571 | C | CA | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
133 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.1495-10437dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450571 | ||||||
| chr6:87450571 | C | CAA | 108 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(105): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-10438_1495-10 others(8): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87450571 | ||||||
| chr6:87450668 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0328 |
4 | HG02109.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-10354G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450668 | |||||||
| chr6:87450668 | G | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1495-10354G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450668 | |||||||
| chr6:87450891 | G | A | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-10131G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450891 | |||||||
| chr6:87450942 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1495-10080C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450942 | |||||||
| chr6:87450987 | C | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-10035C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87450987 | |||||||
| chr6:87451409 | C | A | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-9613C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451409 | |||||||
| chr6:87451501 | C | T | 3 | a0007c0011t0001g0228 a0008c0010t0001g0255 a0008c0010t0001g0256 |
3 | HG02145.hp2 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-9521C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451501 | |||||||
| chr6:87451516 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0328 |
4 | HG02109.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-9506A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451516 | |||||||
| chr6:87451667 | CT | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
99 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1495-9353delT | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87451667 | ||||||
| chr6:87451822 | A | C | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1495-9200A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451822 | |||||||
| chr6:87451832 | A | G | 7 | a0001c0001t0003g0003 a0001c0001t0003g0083 a0001c0001t0003g0084 others(4): Show |
9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-9190A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451832 | |||||||
| chr6:87451868 | T | C | 1 | a0002c0002t0001g0279 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1495-9154T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451868 | |||||||
| chr6:87451876 | G | GAA | 104 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(101): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1495-9133_1495-913 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87451876 | ||||||
| chr6:87451877 | A | G | 5 | a0001c0001t0001g0324 a0001c0001t0001g0326 a0001c0001t0001g0330 others(2): Show |
5 | HG02486.hp2 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-9145A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451877 | |||||||
| chr6:87451905 | A | G | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1495-9117A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87451905 | |||||||
| chr6:87452231 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1495-8791C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87452231 | |||||||
| chr6:87452465 | A | G | 1 | a0002c0002t0001g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1495-8557A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87452465 | |||||||
| chr6:87452472 | C | T | 1 | a0012c0017t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1495-8550C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87452472 | |||||||
| chr6:87452698 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0136 a0001c0001t0001g0207 others(3): Show |
11 | HG00438.hp2 HG02080.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495-8324A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87452698 | |||||||
| chr6:87452989 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1495-8033C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87452989 | |||||||
| chr6:87453221 | G | A | 109 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-7801G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453221 | |||||||
| chr6:87453260 | A | G | 109 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-7762A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453260 | |||||||
| chr6:87453278 | G | T | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-7744G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453278 | |||||||
| chr6:87453495 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1495-7527A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453495 | |||||||
| chr6:87453582 | G | A | 1 | a0001c0007t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1495-7440G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453582 | |||||||
| chr6:87453942 | T | C | 14 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0001g0285 others(11): Show |
14 | HG00597.hp2 NA18945.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.1495-7080T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87453942 | |||||||
| chr6:87454064 | A | G | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1495-6958A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454064 | |||||||
| chr6:87454142 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0019 others(7): Show |
15 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1495-6880G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454142 | |||||||
| chr6:87454418 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(3): Show |
6 | HG00642.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-6604G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454418 | |||||||
| chr6:87454439 | C | A | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1495-6583C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454439 | |||||||
| chr6:87454543 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1495-6479T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454543 | |||||||
| chr6:87454687 | A | T | 1 | a0001c0001t0001g0307 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1495-6335A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454687 | |||||||
| chr6:87454737 | C | T | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-6285C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454737 | |||||||
| chr6:87454784 | A | G | 109 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-6238A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454784 | |||||||
| chr6:87454844 | C | CA | 19 | a0001c0001t0001g0027 a0001c0001t0001g0161 a0001c0001t0001g0164 others(16): Show |
19 | HG00438.hp2 HG00639.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1495-6163dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87454844 | ||||||
| chr6:87454844 | C | CAA | 99 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(96): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1495-6164_1495-616 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87454844 | ||||||
| chr6:87454844 | C | CAAA | 8 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0001c0001t0002g0078 others(5): Show |
8 | HG01169.hp1 HG02145.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1495-6165_1495-616 others(7): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87454844 | ||||||
| chr6:87454844 | CA | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0297 a0001c0001t0001g0309 others(10): Show |
14 | HG00323.hp2 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1495-6163delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87454844 | ||||||
| chr6:87454853 | A | C | 13 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0001g0285 others(10): Show |
13 | HG00597.hp2 NA18945.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.1495-6169A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454853 | |||||||
| chr6:87454860 | C | A | 5 | a0001c0001t0001g0328 a0001c0001t0002g0034 a0001c0001t0002g0039 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-6162C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454860 | |||||||
| chr6:87454888 | A | G | 28 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0241 others(25): Show |
30 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1495-6134A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454888 | |||||||
| chr6:87454924 | T | A | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1495-6098T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454924 | |||||||
| chr6:87454928 | T | A | 1 | a0002c0002t0001g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1495-6094T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454928 | |||||||
| chr6:87454984 | A | G | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-6038A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454984 | |||||||
| chr6:87454990 | T | C | 109 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-6032T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87454990 | |||||||
| chr6:87455051 | T | C | 108 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(105): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1495-5971T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455051 | |||||||
| chr6:87455081 | G | C | 109 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0096 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1495-5941G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455081 | |||||||
| chr6:87455254 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1495-5768A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455254 | |||||||
| chr6:87455370 | T | C | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1495-5652T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455370 | |||||||
| chr6:87455467 | G | C | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-5555G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455467 | |||||||
| chr6:87455507 | C | T | 14 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0043 others(11): Show |
14 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495-5515C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455507 | |||||||
| chr6:87455543 | G | T | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-5479G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455543 | |||||||
| chr6:87455619 | T | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-5403T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455619 | |||||||
| chr6:87455620 | T | C | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1495-5402T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455620 | |||||||
| chr6:87455797 | A | G | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1495-5225A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455797 | |||||||
| chr6:87455831 | A | C | 1 | a0001c0001t0001g0326 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1495-5191A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455831 | |||||||
| chr6:87455979 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1495-5043G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87455979 | |||||||
| chr6:87456055 | C | A | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1495-4967C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456055 | |||||||
| chr6:87456228 | T | C | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1495-4794T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456228 | |||||||
| chr6:87456234 | C | A | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-4788C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456234 | |||||||
| chr6:87456338 | A | C | 104 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(101): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1495-4684A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456338 | |||||||
| chr6:87456479 | T | G | 1 | a0001c0003t0001g0165 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1495-4543T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456479 | |||||||
| chr6:87456561 | G | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
62 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1495-4461G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456561 | |||||||
| chr6:87456831 | A | G | 8 | a0001c0001t0001g0023 a0001c0001t0001g0297 a0001c0001t0001g0309 others(5): Show |
9 | HG00323.hp2 HG01256.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1495-4191A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87456831 | |||||||
| chr6:87457009 | G | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0230 |
3 | HG02615.hp1 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1495-4013G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457009 | |||||||
| chr6:87457019 | A | G | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-4003A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457019 | |||||||
| chr6:87457022 | T | C | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-4000T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457022 | |||||||
| chr6:87457023 | G | A | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-3999G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457023 | |||||||
| chr6:87457033 | C | T | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1495-3989C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457033 | |||||||
| chr6:87457145 | C | A | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1495-3877C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457145 | |||||||
| chr6:87457149 | C | CA | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
101 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.1495-3856dupA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87457149 | ||||||
| chr6:87457149 | C | CAA | 17 | a0001c0001t0001g0300 a0002c0002t0001g0249 a0002c0002t0001g0264 others(14): Show |
18 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1495-3857_1495-385 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87457149 | ||||||
| chr6:87457149 | CA | C | 104 | a0001c0001t0001g0096 a0001c0001t0001g0112 a0001c0001t0001g0131 others(101): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1495-3856delA | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87457149 | ||||||
| chr6:87457149 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0311 |
3 | NA18947.hp2 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1495-3867_1495-385 others(16): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 87457149 | ||||||
| chr6:87457198 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-3824T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457198 | |||||||
| chr6:87457206 | G | T | 105 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(102): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1495-3816G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457206 | |||||||
| chr6:87457318 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1495-3704T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457318 | |||||||
| chr6:87457332 | G | A | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-3690G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457332 | |||||||
| chr6:87457446 | A | T | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1495-3576A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457446 | |||||||
| chr6:87457613 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0112 others(19): Show |
28 | HG00438.hp1 HG00438.hp2 HG02040.hp1 others(25): Show |
intron_variant | MODIFIER | c.1495-3409A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457613 | |||||||
| chr6:87457619 | A | G | 1 | a0002c0002t0001g0279 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1495-3403A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457619 | |||||||
| chr6:87457647 | G | A | 4 | a0003c0004t0001g0020 a0003c0004t0001g0243 a0003c0004t0001g0244 others(1): Show |
5 | HG00741.hp1 HG01358.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-3375G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457647 | |||||||
| chr6:87457767 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1495-3255A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457767 | |||||||
| chr6:87457771 | T | A | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-3251T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87457771 | |||||||
| chr6:87458125 | C | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0083 a0001c0001t0003g0085 others(3): Show |
8 | HG01891.hp2 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1495-2897C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458125 | |||||||
| chr6:87458179 | C | T | 222 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1495-2843C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458179 | |||||||
| chr6:87458235 | G | C | 2 | a0001c0008t0002g0026 a0001c0008t0002g0247 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1495-2787G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458235 | |||||||
| chr6:87458280 | A | G | 3 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02922.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1495-2742A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458280 | |||||||
| chr6:87458368 | C | A | 1 | a0001c0001t0002g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1495-2654C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458368 | |||||||
| chr6:87458371 | T | C | 1 | a0007c0011t0001g0228 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1495-2651T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458371 | |||||||
| chr6:87458517 | C | CAT | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-2505_1495-250 others(6): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458517 | |||||||
| chr6:87458517 | C | T | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1495-2505C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458517 | |||||||
| chr6:87458596 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1495-2426G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458596 | |||||||
| chr6:87458729 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1495-2293G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458729 | |||||||
| chr6:87458825 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1495-2197C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87458825 | |||||||
| chr6:87459260 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02922.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-1762G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459260 | |||||||
| chr6:87459274 | A | C | 1 | a0002c0002t0001g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1495-1748A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459274 | |||||||
| chr6:87459327 | C | G | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-1695C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459327 | |||||||
| chr6:87459394 | T | A | 1 | a0001c0001t0001g0332 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1495-1628T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459394 | |||||||
| chr6:87459568 | A | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-1454A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459568 | |||||||
| chr6:87459766 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1495-1256G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459766 | |||||||
| chr6:87459771 | G | A | 2 | a0003c0004t0001g0020 a0003c0004t0001g0245 |
3 | HG00741.hp1 HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1495-1251G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459771 | |||||||
| chr6:87459778 | G | A | 100 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(97): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1495-1244G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459778 | |||||||
| chr6:87459959 | A | C | 2 | a0006c0009t0002g0069 a0006c0009t0002g0104 |
2 | HG00099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1495-1063A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87459959 | |||||||
| chr6:87460239 | T | A | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-783T>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460239 | |||||||
| chr6:87460240 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-782T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460240 | |||||||
| chr6:87460245 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-777A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460245 | |||||||
| chr6:87460247 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-775T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460247 | |||||||
| chr6:87460257 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-765T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460257 | |||||||
| chr6:87460258 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-764G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460258 | |||||||
| chr6:87460260 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1495-762G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460260 | |||||||
| chr6:87460520 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1495-502T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460520 | |||||||
| chr6:87460540 | A | G | 93 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1495-482A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460540 | |||||||
| chr6:87460632 | A | T | 8 | a0001c0001t0001g0315 a0001c0007t0001g0239 a0001c0007t0001g0240 others(5): Show |
9 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-390A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460632 | |||||||
| chr6:87460674 | G | A | 7 | a0001c0001t0003g0003 a0001c0001t0003g0083 a0001c0001t0003g0084 others(4): Show |
9 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-348G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460674 | |||||||
| chr6:87460771 | G | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0159 others(1): Show |
4 | HG02630.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-251G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460771 | |||||||
| chr6:87460938 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0318 |
2 | HG01109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1495-84T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460938 | |||||||
| chr6:87460992 | A | T | 107 | a0001c0001t0001g0096 a0001c0001t0002g0002 a0001c0001t0002g0008 others(104): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-30A>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460992 | |||||||
| chr6:87460996 | C | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0235 a0001c0001t0001g0236 |
5 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495-26C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 11/12 | chr6 | 87460996 | |||||||
| chr6:87461205 | G | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0230 |
3 | HG02615.hp1 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1638+40G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461205 | |||||||
| chr6:87461245 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1638+80A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461245 | |||||||
| chr6:87461621 | T | G | 1 | a0012c0017t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1638+456T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461621 | |||||||
| chr6:87461639 | G | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1638+474G>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461639 | |||||||
| chr6:87461682 | A | G | 1 | a0004c0005t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1638+517A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461682 | |||||||
| chr6:87461689 | AC | A | 102 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(99): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1638+525delC | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461689 | |||||||
| chr6:87461690 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1638+525C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461690 | |||||||
| chr6:87461726 | T | TTA | 335 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(332): Show |
370 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.1638+562_1638+563i others(4): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 87461726 | ||||||
| chr6:87461808 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1638+643G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461808 | |||||||
| chr6:87461819 | A | G | 105 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(102): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1638+654A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461819 | |||||||
| chr6:87461890 | C | T | 1 | a0011c0016t0001g0327 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1638+725C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461890 | |||||||
| chr6:87461909 | G | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0087 a0001c0001t0001g0096 others(13): Show |
17 | HG00323.hp1 HG00558.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1638+744G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87461909 | |||||||
| chr6:87462107 | T | G | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1638+942T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462107 | |||||||
| chr6:87462306 | C | T | 1 | a0003c0004t0001g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1638+1141C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462306 | |||||||
| chr6:87462526 | A | AGTACCTC others(10): Show |
1 | a0001c0001t0001g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1638+1381_1638+139 others(21): Show |
CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 87462526 | ||||||
| chr6:87462567 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1638+1402C>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462567 | |||||||
| chr6:87462613 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1639-1407A>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462613 | |||||||
| chr6:87462667 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1639-1353T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462667 | |||||||
| chr6:87462709 | A | C | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1639-1311A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462709 | |||||||
| chr6:87462760 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0004g0018 a0001c0001t0004g0230 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639-1260C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87462760 | |||||||
| chr6:87463037 | G | T | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1639-983G>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463037 | |||||||
| chr6:87463330 | C | T | 104 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(101): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1639-690C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463330 | |||||||
| chr6:87463339 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1639-681G>A | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463339 | |||||||
| chr6:87463436 | C | G | 103 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(100): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1639-584C>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463436 | |||||||
| chr6:87463449 | T | C | 222 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1639-571T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463449 | |||||||
| chr6:87463481 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1639-539C>T | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463481 | |||||||
| chr6:87463587 | T | C | 1 | a0007c0011t0002g0227 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1639-433T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463587 | |||||||
| chr6:87463744 | T | G | 2 | a0001c0014t0002g0025 a0007c0011t0002g0227 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1639-276T>G | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463744 | |||||||
| chr6:87463928 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1639-92A>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87463928 | |||||||
| chr6:87464017 | T | C | 2 | a0008c0010t0001g0255 a0008c0010t0001g0256 |
2 | HG02145.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.1639-3T>C | CFAP206 | ENSG00000272514.6 | transcript | ENST00000369562.9 | protein_coding | 12/12 | chr6 | 87464017 |