Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129881 |
| ensemblid | ENSG00000154479.13 |
| hgncid | 25064 |
| symbol | CFAP210 |
| name | cilia and flagella associated protein 210 |
| refseq_nuc | NM_001085447.2 |
| refseq_prot | NP_001078916.1 |
| ensembl_nuc | ENST00000447353.6 |
| ensembl_prot | ENSP00000391504.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 169645425 |
| end | 169694405 |
| strand | - |
| ver | v1.2 |
| region | chr2:169645425-169694405 |
| region5000 | chr2:169640425-169699405 |
| regionname0 | CFAP210_chr2_169645425_169694405 |
| regionname5000 | CFAP210_chr2_169640425_169699405 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 552 | 311 | 63 | 49 | 154 | 11 | 32 | 124 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0002 | 0/0 | 552 | 27 | 0 | 0 | 23 | 1 | 3 | 17 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0003 | 0/0 | 552 | 18 | 6 | 3 | 4 | 1 | 4 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0004 | 0/0 | 552 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0005 | 0/0 | 552 | 5 | 1 | 0 | 0 | 1 | 3 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0006 | 0/0 | 552 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0007 | 0/0 | 550 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(545): Show |
chr2 | 169640425 | 169699405 |
| a0008 | 0/0 | 552 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0009 | 0/0 | 552 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0010 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0011 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0012 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0013 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0014 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| a0015 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | MDTSS others(547): Show |
chr2 | 169640425 | 169699405 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1656 | 305 | 58 | 48 | 154 | 11 | 32 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0001c0007 | 0/0 | 1656 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0001c0008 | 0/0 | 1656 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0002c0002 | 0/0 | 1656 | 27 | 0 | 0 | 23 | 1 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0003c0003 | 0/0 | 1656 | 18 | 6 | 3 | 4 | 1 | 4 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0004c0004 | 0/0 | 1656 | 12 | 10 | 2 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0005c0005 | 0/0 | 1656 | 5 | 1 | 0 | 0 | 1 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0006c0006 | 0/0 | 1656 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0007c0009 | 0/0 | 1650 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1645): Show |
chr2 | 169640425 | 169699405 | ||
| a0008c0010 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0009c0011 | 0/0 | 1656 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0010c0016 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0011c0014 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0012c0013 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0013c0017 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0014c0015 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 | ||
| a0015c0012 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | ATGGA others(1651): Show |
chr2 | 169640425 | 169699405 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2153 | 253 | 46 | 30 | 142 | 9 | 25 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0001c0001t0002 | 0/0 | 2153 | 26 | 10 | 7 | 3 | 2 | 4 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0001c0001t0003 | 0/1 | 2153 | 25 | 1 | 11 | 9 | 0 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0001c0001t0004 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0001c0007t0002 | 0/0 | 2153 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0001c0008t0001 | 0/0 | 2153 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0002c0002t0001 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0002c0002t0002 | 0/0 | 2153 | 26 | 0 | 0 | 22 | 1 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0003c0003t0002 | 0/0 | 2153 | 18 | 6 | 3 | 4 | 1 | 4 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0004c0004t0002 | 0/0 | 2153 | 12 | 10 | 2 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0005c0005t0002 | 0/0 | 2153 | 5 | 1 | 0 | 0 | 1 | 3 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0006c0006t0002 | 0/0 | 2153 | 4 | 4 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0007c0009t0001 | 0/0 | 2147 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2142): Show |
chr2 | 169640425 | 169699405 |
| a0008c0010t0001 | 0/0 | 2153 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0009c0011t0001 | 0/0 | 2153 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0010c0016t0002 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0011c0014t0003 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0012c0013t0002 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0013c0017t0002 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0014c0015t0001 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| a0015c0012t0001 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | GTGGT others(2148): Show |
chr2 | 169640425 | 169699405 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0015 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0007t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0007t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0007t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0008t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0008t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0001c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0004c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0005c0005t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0005c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0005c0005t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0005c0005t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0006c0006t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0006c0006t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0006c0006t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0007c0009t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0007c0009t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0007c0009t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0008c0010t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0008c0010t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0009c0011t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0009c0011t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0010c0016t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0011c0014t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0012c0013t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0013c0017t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0014c0015t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| a0015c0012t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0336 | EUR | GBR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00280 | hp1 | a0003 | c0003 | t0002 | g0053 | EUR | FIN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00323 | hp1 | a0005 | c0005 | t0002 | g0048 | EUR | FIN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | FIN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00733 | hp2 | a0004 | c0004 | t0002 | g0072 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01099 | hp1 | a0003 | c0003 | t0002 | g0063 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0006 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01496 | hp2 | a0001 | c0007 | t0002 | g0064 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0005 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01891 | hp1 | a0004 | c0004 | t0002 | g0071 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0051 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02055 | hp2 | a0004 | c0004 | t0002 | g0006 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CDX | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02258 | hp1 | a0006 | c0006 | t0002 | g0013 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02523 | hp2 | a0011 | c0014 | t0003 | g0098 | EAS | KHV | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02572 | hp1 | a0012 | c0013 | t0002 | g0076 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02615 | hp1 | a0005 | c0005 | t0002 | g0050 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0136 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02647 | hp1 | a0001 | c0008 | t0001 | g0138 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02698 | hp2 | a0005 | c0005 | t0002 | g0049 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02717 | hp1 | a0008 | c0010 | t0001 | g0278 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02809 | hp2 | a0003 | c0003 | t0002 | g0005 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02886 | hp2 | a0004 | c0004 | t0002 | g0074 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02895 | hp1 | a0001 | c0007 | t0002 | g0066 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02896 | hp2 | a0004 | c0004 | t0002 | g0061 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02922 | hp1 | a0003 | c0003 | t0002 | g0005 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02922 | hp2 | a0004 | c0004 | t0002 | g0067 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02965 | hp2 | a0004 | c0004 | t0002 | g0069 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0058 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03139 | hp2 | a0006 | c0006 | t0002 | g0013 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03195 | hp2 | a0001 | c0007 | t0002 | g0065 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03209 | hp1 | a0008 | c0010 | t0001 | g0279 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03209 | hp2 | a0007 | c0009 | t0001 | g0238 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03225 | hp2 | a0007 | c0009 | t0001 | g0237 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0052 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03453 | hp1 | a0004 | c0004 | t0002 | g0075 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03490 | hp2 | a0005 | c0005 | t0002 | g0012 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03492 | hp2 | a0005 | c0005 | t0002 | g0012 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03540 | hp2 | a0004 | c0004 | t0002 | g0068 | AFR | GWD | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03654 | hp2 | a0003 | c0003 | t0002 | g0056 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0057 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04228 | hp1 | a0003 | c0003 | t0002 | g0062 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18522 | hp1 | a0006 | c0006 | t0002 | g0100 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | CHB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18952 | hp2 | a0014 | c0015 | t0001 | g0292 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18967 | hp1 | a0009 | c0011 | t0001 | g0201 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18987 | hp2 | a0009 | c0011 | t0001 | g0189 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19003 | hp1 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19009 | hp1 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19011 | hp2 | a0015 | c0012 | t0001 | g0188 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19030 | hp1 | a0006 | c0006 | t0002 | g0099 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19043 | hp1 | a0004 | c0004 | t0002 | g0070 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0059 | AFR | YRI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ASW | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20129 | hp2 | a0007 | c0009 | t0001 | g0236 | AFR | ASW | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | TSI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02109 | hp1 | a0010 | c0016 | t0002 | g0073 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02486 | hp2 | a0001 | c0008 | t0001 | g0137 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0060 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | USA | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| HG06807 | hp2 | a0013 | c0017 | t0002 | g0132 | AFR | USA | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | USA | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA20300 | hp2 | a0004 | c0004 | t0002 | g0006 | AFR | USA | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | LWK | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0108 | REF | REF | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0015 | REF | REF | CFAP210_chr2_169640425_169699405 | CFAP210 | chr2 | 169640425 | 169699405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169645891 | G | A | 3 | a0003 a0005 a0012 |
24 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(21): Show |
missense_variant | MODERATE | c.1609C>T | p.Pro537Ser | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 1687/2153 | 1609/1659 | 537/552 | chr2 | 169645891 | |||
| chr2:169645905 | T | C | 2 | a0005 a0012 |
6 | HG00323.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.1595A>G | p.Tyr532Cys | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 1673/2153 | 1595/1659 | 532/552 | chr2 | 169645905 | |||
| chr2:169645999 | G | A | 1 | a0006 | 4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.1501C>T | p.Pro501Ser | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 1579/2153 | 1501/1659 | 501/552 | chr2 | 169645999 | |||
| chr2:169646137 | C | A | 1 | a0015 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1363G>T | p.Asp455Tyr | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 1441/2153 | 1363/1659 | 455/552 | chr2 | 169646137 | |||
| chr2:169649190 | G | C | 1 | a0008 | 2 | HG02717.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.1309C>G | p.Gln437Glu | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/9 | 1387/2153 | 1309/1659 | 437/552 | chr2 | 169649190 | |||
| chr2:169649285 | G | C | 4 | a0004 a0010 a0012 others(1): Show |
15 | HG00733.hp2 HG01255.hp1 HG01891.hp1 others(12): Show |
missense_variant | MODERATE | c.1214C>G | p.Ala405Gly | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/9 | 1292/2153 | 1214/1659 | 405/552 | chr2 | 169649285 | |||
| chr2:169649312 | T | C | 1 | a0009 | 2 | NA18967.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.1187A>G | p.Lys396Arg | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/9 | 1265/2153 | 1187/1659 | 396/552 | chr2 | 169649312 | |||
| chr2:169650384 | TTTTCTC | T | 1 | a0007 | 3 | HG03209.hp2 HG03225.hp2 NA20129.hp2 |
disruptive_inframe_deletion | MODERATE | c.1091_1096delGAGAAA | p.Arg364_Glu365del | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/9 | 1174/2153 | 1091/1659 | 364/552 | chr2 | 169650384 | |||
| chr2:169650407 | T | A | 1 | a0011 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1074A>T | p.Glu358Asp | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/9 | 1152/2153 | 1074/1659 | 358/552 | chr2 | 169650407 | |||
| chr2:169654141 | C | T | 1 | a0002 | 27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
missense_variant | MODERATE | c.893G>A | p.Arg298Lys | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/9 | 971/2153 | 893/1659 | 298/552 | chr2 | 169654141 | |||
| chr2:169674945 | T | A | 1 | a0014 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.390A>T | p.Lys130Asn | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 3/9 | 468/2153 | 390/1659 | 130/552 | chr2 | 169674945 | |||
| chr2:169681026 | T | C | 1 | a0010 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.275A>G | p.His92Arg | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/9 | 353/2153 | 275/1659 | 92/552 | chr2 | 169681026 | |||
| chr2:169694299 | C | A | 1 | a0013 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.29G>T | p.Arg10Leu | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/9 | 107/2153 | 29/1659 | 10/552 | chr2 | 169694299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169646078 | A | G | 1 | a0001c0008 | 3 | HG02486.hp2 HG02630.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.1422T>C | p.Tyr474Tyr | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 1500/2153 | 1422/1659 | 474/552 | chr2 | 169646078 | |||
| chr2:169681103 | T | C | 1 | a0007c0009 | 3 | HG03209.hp2 HG03225.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.198A>G | p.Thr66Thr | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/9 | 276/2153 | 198/1659 | 66/552 | chr2 | 169681103 | |||
| chr2:169681151 | A | G | 1 | a0001c0007 | 3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.150T>C | p.Ile50Ile | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/9 | 228/2153 | 150/1659 | 50/552 | chr2 | 169681151 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169645656 | C | T | 1 | a0001c0001t0004 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 185 | chr2 | 169645656 | ||||||
| chr2:169645833 | A | T | 2 | a0001c0001t0003 a0011c0014t0003 |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*8T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 9/9 | 8 | chr2 | 169645833 | ||||||
| chr2:169694329 | A | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0007t0002 others(9): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
5_prime_UTR_variant | MODIFIER | c.-2T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/9 | 2 | chr2 | 169694329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:169646216 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1318-34A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646216 | |||||||
| chr2:169646265 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1318-83C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646265 | |||||||
| chr2:169646316 | A | G | 32 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(29): Show |
38 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1318-134T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646316 | |||||||
| chr2:169646376 | C | T | 5 | a0003c0003t0002g0005 a0003c0003t0002g0058 a0003c0003t0002g0059 others(2): Show |
7 | HG01099.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318-194G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646376 | |||||||
| chr2:169646409 | A | G | 204 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1318-227T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646409 | |||||||
| chr2:169646634 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1318-452T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646634 | |||||||
| chr2:169646669 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1318-487C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646669 | |||||||
| chr2:169646712 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00735.hp2 HG01069.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1318-530C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646712 | |||||||
| chr2:169646721 | G | T | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1318-539C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646721 | |||||||
| chr2:169646788 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1318-606C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646788 | |||||||
| chr2:169646850 | C | G | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1318-668G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646850 | |||||||
| chr2:169646900 | T | C | 8 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1318-718A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646900 | |||||||
| chr2:169646989 | G | A | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1318-807C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169646989 | |||||||
| chr2:169647192 | C | CA | 124 | a0001c0001t0001g0025 a0001c0001t0001g0139 a0001c0001t0001g0266 others(121): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1318-1011dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647192 | |||||||
| chr2:169647192 | C | CAA | 7 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
7 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318-1012_1318-101 others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647192 | |||||||
| chr2:169647558 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(40): Show |
50 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.1318-1376A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647558 | |||||||
| chr2:169647559 | GT | G | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1318-1378delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647559 | |||||||
| chr2:169647589 | G | A | 1 | a0002c0002t0002g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1318-1407C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647589 | |||||||
| chr2:169647602 | G | A | 13 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(10): Show |
13 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1318-1420C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647602 | |||||||
| chr2:169647722 | T | TTA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
9 | HG02451.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1317+1458_1317+145 others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647722 | |||||||
| chr2:169647730 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1317+1452G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647730 | |||||||
| chr2:169647822 | G | A | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1317+1360C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647822 | |||||||
| chr2:169647902 | C | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1317+1280G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647902 | |||||||
| chr2:169647954 | G | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317+1228C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169647954 | |||||||
| chr2:169648017 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1317+1165C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648017 | |||||||
| chr2:169648126 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1317+1056C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648126 | |||||||
| chr2:169648162 | C | CA | 30 | a0001c0001t0001g0020 a0001c0001t0001g0135 a0001c0001t0001g0148 others(27): Show |
31 | HG00423.hp2 HG00609.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1317+1019dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CA | C | 24 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(21): Show |
24 | HG00099.hp2 HG01169.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1317+1019delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAA | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0001g0297 others(6): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317+1018_1317+101 others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAA | C | 13 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0002g0103 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1317+1017_1317+101 others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAA | C | 22 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0274 others(19): Show |
22 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1317+1016_1317+101 others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAA | C | 11 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(8): Show |
11 | HG02074.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1317+1014_1317+101 others(10): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAAA | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1317+1013_1317+101 others(11): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAAA others(3): Show |
C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1317+1010_1317+101 others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1317+1007_1317+101 others(17): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0002g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1317+1005_1317+101 others(19): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648162 | CAAAAAAA others(9): Show |
C | 30 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(27): Show |
32 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1317+1004_1317+101 others(20): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648162 | |||||||
| chr2:169648190 | A | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1317+992T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648190 | |||||||
| chr2:169648229 | C | T | 5 | a0003c0003t0002g0005 a0003c0003t0002g0058 a0003c0003t0002g0059 others(2): Show |
7 | HG01099.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1317+953G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648229 | |||||||
| chr2:169648427 | C | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1317+755G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648427 | |||||||
| chr2:169648446 | TTTATG | T | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1317+731_1317+735d others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648446 | |||||||
| chr2:169648485 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1317+697A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648485 | |||||||
| chr2:169648542 | G | C | 1 | a0002c0002t0002g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1317+640C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648542 | |||||||
| chr2:169648674 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1317+508A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648674 | |||||||
| chr2:169648798 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
93 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1317+384A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648798 | |||||||
| chr2:169648819 | GAT | G | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1317+361_1317+362d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648819 | |||||||
| chr2:169648879 | A | C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG00609.hp1 NA18945.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317+303T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169648879 | |||||||
| chr2:169649097 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1317+85T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169649097 | |||||||
| chr2:169649120 | A | G | 1 | a0001c0001t0001g0307 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1317+62T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169649120 | |||||||
| chr2:169649174 | G | A | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
splice_region_variant&intron_variant | LOW | c.1317+8C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 8/8 | chr2 | 169649174 | |||||||
| chr2:169649487 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1153-141C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169649487 | |||||||
| chr2:169649500 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1153-154C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169649500 | |||||||
| chr2:169649922 | C | CA | 85 | a0001c0001t0001g0025 a0001c0001t0001g0139 a0001c0001t0001g0242 others(82): Show |
93 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1152+406dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169649922 | |||||||
| chr2:169649922 | C | CAA | 61 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
72 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1152+405_1152+406d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169649922 | |||||||
| chr2:169649943 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1152+386T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169649943 | |||||||
| chr2:169650069 | C | T | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1152+260G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169650069 | |||||||
| chr2:169650134 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1152+195A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169650134 | |||||||
| chr2:169650210 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0177 |
2 | NA18972.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1152+119T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 7/8 | chr2 | 169650210 | |||||||
| chr2:169650570 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.960-49T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650570 | |||||||
| chr2:169650642 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.960-121A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650642 | |||||||
| chr2:169650734 | C | CTG | 17 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0142 others(14): Show |
19 | HG00140.hp1 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.960-215_960-214dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTG | 50 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0021 others(47): Show |
60 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.960-217_960-214dup others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTG | 46 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0020 others(43): Show |
54 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.960-219_960-214dup others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTGT others(1): Show |
21 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0177 others(18): Show |
21 | HG00609.hp1 HG02145.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.960-221_960-214dup others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTGT others(3): Show |
26 | a0001c0001t0001g0018 a0001c0001t0001g0176 a0001c0001t0002g0029 others(23): Show |
32 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.960-223_960-214dup others(10): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTGT others(5): Show |
11 | a0001c0001t0001g0139 a0001c0001t0002g0034 a0001c0008t0001g0137 others(8): Show |
11 | HG00558.hp1 HG00733.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.960-225_960-214dup others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0199 a0001c0008t0001g0136 a0005c0005t0002g0012 |
4 | HG02129.hp2 HG02630.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-227_960-214dup others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | C | CTGTGTGT others(9): Show |
2 | a0004c0004t0002g0071 a0006c0006t0002g0013 |
3 | HG01891.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.960-229_960-214dup others(16): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | CTG | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(53): Show |
66 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.960-215_960-214del others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | CTGTG | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0299 a0001c0001t0001g0334 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.960-217_960-214del others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | CTGTGTG | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(47): Show |
57 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(54): Show |
intron_variant | MODIFIER | c.960-219_960-214del others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | CTGTGTGT others(1): Show |
C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0276 a0001c0001t0001g0277 others(6): Show |
10 | HG02451.hp1 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.960-221_960-214del others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650734 | CTGTGTGT others(3): Show |
C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.960-223_960-214del others(10): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650734 | |||||||
| chr2:169650829 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.960-308A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650829 | |||||||
| chr2:169650926 | C | T | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.960-405G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169650926 | |||||||
| chr2:169651005 | C | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(244): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.960-484G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651005 | |||||||
| chr2:169651098 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.960-577C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651098 | |||||||
| chr2:169651205 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 |
3 | HG00140.hp2 HG01256.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.960-684G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651205 | |||||||
| chr2:169651226 | G | GA | 29 | a0001c0001t0001g0151 a0001c0001t0001g0191 a0001c0001t0001g0217 others(26): Show |
29 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.960-706dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | G | GAA | 11 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0271 others(8): Show |
12 | HG01891.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.960-707_960-706dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | G | GAAA | 10 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(7): Show |
12 | HG01099.hp1 HG01884.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.960-708_960-706dup others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | G | GAAAA | 48 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(45): Show |
52 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.960-709_960-706dup others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | G | GAAAAA | 8 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.960-710_960-706dup others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | G | GGAA | 20 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(17): Show |
25 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.960-706_960-705ins others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651226 | GA | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0026 others(59): Show |
71 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.960-706delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651226 | |||||||
| chr2:169651255 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.960-734G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651255 | |||||||
| chr2:169651266 | G | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.960-745C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651266 | |||||||
| chr2:169651407 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.960-886A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651407 | |||||||
| chr2:169651794 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.960-1273G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651794 | |||||||
| chr2:169651875 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0161 a0001c0001t0001g0234 others(9): Show |
13 | HG02056.hp2 HG02135.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.960-1355dupA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651875 | |||||||
| chr2:169651875 | CTT | C | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.960-1356_960-1355d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651875 | |||||||
| chr2:169651884 | T | G | 46 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(43): Show |
46 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.960-1363A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651884 | |||||||
| chr2:169651887 | T | G | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.960-1366A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169651887 | |||||||
| chr2:169652020 | C | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.960-1499G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652020 | |||||||
| chr2:169652284 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.960-1763A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652284 | |||||||
| chr2:169652375 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.959+1700T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652375 | |||||||
| chr2:169652380 | T | C | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.959+1695A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652380 | |||||||
| chr2:169652388 | G | T | 1 | a0004c0004t0002g0061 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.959+1687C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652388 | |||||||
| chr2:169652397 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.959+1678C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652397 | |||||||
| chr2:169652443 | A | G | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.959+1632T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652443 | |||||||
| chr2:169652448 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
93 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.959+1627G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652448 | |||||||
| chr2:169652518 | C | T | 21 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(18): Show |
21 | HG00140.hp2 HG00558.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.959+1557G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652518 | |||||||
| chr2:169652721 | C | T | 43 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(40): Show |
44 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.959+1354G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652721 | |||||||
| chr2:169652748 | C | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0300 a0001c0001t0001g0301 others(11): Show |
16 | HG00673.hp1 HG01255.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+1327G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652748 | |||||||
| chr2:169652761 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0300 a0001c0001t0001g0301 others(11): Show |
16 | HG00673.hp1 HG01255.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.959+1314G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652761 | |||||||
| chr2:169652770 | C | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+1305G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652770 | |||||||
| chr2:169652841 | A | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.959+1234T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652841 | |||||||
| chr2:169652857 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.959+1218C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652857 | |||||||
| chr2:169652864 | G | C | 10 | a0003c0003t0002g0011 a0003c0003t0002g0047 a0003c0003t0002g0051 others(7): Show |
11 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+1211C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652864 | |||||||
| chr2:169652917 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.959+1158C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652917 | |||||||
| chr2:169652931 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(243): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.959+1144A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652931 | |||||||
| chr2:169652944 | A | G | 5 | a0001c0001t0001g0146 a0001c0001t0002g0032 a0001c0001t0002g0033 others(2): Show |
5 | HG02280.hp2 NA18967.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+1131T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652944 | |||||||
| chr2:169652992 | T | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.959+1083A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652992 | |||||||
| chr2:169652999 | C | CA | 7 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0192 others(4): Show |
7 | HG00280.hp2 HG00558.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+1075dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652999 | |||||||
| chr2:169652999 | C | CAAAAAAA others(3): Show |
1 | a0008c0010t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.959+1066_959+1075d others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652999 | |||||||
| chr2:169652999 | CAA | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0001c0001t0001g0175 others(1): Show |
6 | HG02647.hp2 NA18980.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+1074_959+1075d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169652999 | |||||||
| chr2:169653021 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+1054T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653021 | |||||||
| chr2:169653023 | A | AATATATA others(3): Show |
1 | a0001c0001t0002g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.959+1051_959+1052i others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653023 | |||||||
| chr2:169653023 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+1052T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653023 | |||||||
| chr2:169653023 | AAAAAAAA others(11): Show |
A | 1 | a0002c0002t0002g0086 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.959+1034_959+1051d others(20): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653023 | |||||||
| chr2:169653024 | AAAAAAAT others(10): Show |
A | 1 | a0002c0002t0002g0093 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.959+1034_959+1050d others(19): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653024 | |||||||
| chr2:169653025 | A | T | 9 | a0001c0001t0001g0277 a0001c0001t0002g0101 a0001c0001t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+1050T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653025 | |||||||
| chr2:169653025 | AAAAAATA others(3): Show |
A | 1 | a0001c0008t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.959+1040_959+1049d others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653025 | |||||||
| chr2:169653025 | AAAAAATA others(11): Show |
A | 1 | a0001c0001t0001g0295 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.959+1032_959+1049d others(20): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653025 | |||||||
| chr2:169653025 | AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0336 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.959+1030_959+1049d others(22): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653025 | |||||||
| chr2:169653026 | AAAAATAT others(6): Show |
A | 1 | a0007c0009t0001g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.959+1036_959+1048d others(15): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653026 | |||||||
| chr2:169653027 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.959+1047_959+1048i others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | A | T | 9 | a0001c0001t0001g0277 a0001c0001t0002g0101 a0001c0001t0002g0102 others(6): Show |
9 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+1048T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAAT | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0135 a0001c0001t0001g0165 others(3): Show |
6 | HG01070.hp2 HG01243.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+1044_959+1047d others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAATATA others(3): Show |
A | 2 | a0001c0008t0001g0138 a0007c0009t0001g0236 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.959+1038_959+1047d others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAATATA others(5): Show |
A | 2 | a0001c0008t0001g0136 a0003c0003t0002g0047 |
2 | HG02630.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.959+1036_959+1047d others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAATATA others(7): Show |
A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0274 a0002c0002t0002g0004 others(1): Show |
5 | HG01099.hp1 HG01891.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+1034_959+1047d others(16): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAATATA others(9): Show |
A | 5 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0081 others(2): Show |
5 | HG00140.hp1 HG00621.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+1032_959+1047d others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653027 | AAAATATA others(11): Show |
A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0306 a0001c0001t0001g0310 others(5): Show |
8 | HG01175.hp2 HG02602.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+1030_959+1047d others(20): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653027 | |||||||
| chr2:169653028 | AAAT | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0146 a0001c0001t0001g0179 others(3): Show |
6 | NA18939.hp1 NA18953.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+1044_959+1046d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATAT | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0152 a0001c0001t0001g0156 others(6): Show |
9 | HG01109.hp1 HG01358.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+1042_959+1046d others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATATAT others(4): Show |
A | 1 | a0002c0002t0002g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.959+1036_959+1046d others(13): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATATAT others(6): Show |
A | 8 | a0002c0002t0002g0007 a0002c0002t0002g0082 a0002c0002t0002g0094 others(5): Show |
10 | HG01884.hp1 HG02559.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.959+1034_959+1046d others(15): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATATAT others(8): Show |
A | 6 | a0002c0002t0002g0004 a0002c0002t0002g0088 a0002c0002t0002g0089 others(3): Show |
6 | HG00558.hp2 NA18952.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+1032_959+1046d others(17): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATATAT others(10): Show |
A | 3 | a0001c0001t0001g0303 a0001c0001t0001g0307 a0001c0001t0001g0322 |
3 | HG00438.hp2 NA18969.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.959+1030_959+1046d others(19): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653028 | AAATATAT others(12): Show |
A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0282 a0001c0001t0001g0296 others(5): Show |
8 | HG01433.hp1 HG03704.hp1 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+1028_959+1046d others(21): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653028 | |||||||
| chr2:169653029 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0110 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(34): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(26): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.959+1045_959+1046i others(24): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0003g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(32): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(22): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(13): Show |
1 | a0011c0014t0003g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(22): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0003g0130 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.959+1045_959+1046i others(23): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0003g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(25): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0003g0122 a0001c0001t0003g0129 |
2 | HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.959+1045_959+1046i others(22): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0126 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.959+1045_959+1046i others(21): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0003g0125 a0001c0001t0003g0131 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.959+1045_959+1046i others(23): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(21): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.959+1045_959+1046i others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAAATA others(9): Show |
1 | a0001c0001t0002g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | AAAAATAT others(16): Show |
1 | a0001c0001t0003g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.959+1045_959+1046i others(25): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0287 a0001c0001t0004g0286 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.959+1045_959+1046i others(13): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | A | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0160 others(14): Show |
19 | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.959+1046T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AAT | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(17): Show |
20 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+1044_959+1045d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATAT | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(22): Show |
28 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.959+1042_959+1045d others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATATAT | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(19): Show |
25 | HG00423.hp2 HG00735.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.959+1040_959+1045d others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATATATA others(5): Show |
A | 8 | a0001c0001t0001g0142 a0003c0003t0002g0011 a0003c0003t0002g0056 others(5): Show |
10 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+1034_959+1045d others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATATATA others(7): Show |
A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG01123.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.959+1032_959+1045d others(16): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATATATA others(9): Show |
A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0302 |
2 | HG01516.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.959+1030_959+1045d others(18): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653029 | AATATATA others(11): Show |
A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
42 | HG00323.hp2 HG00639.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.959+1028_959+1045d others(20): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653029 | |||||||
| chr2:169653030 | AT | A | 12 | a0001c0001t0001g0163 a0001c0001t0001g0194 a0001c0001t0001g0226 others(9): Show |
12 | HG01106.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+1044delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATAT | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(17): Show |
20 | HG00673.hp2 HG01168.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+1042_959+1044d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATAT | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
24 | HG00099.hp2 HG01074.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.959+1040_959+1044d others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0149 a0001c0001t0001g0210 others(1): Show |
4 | HG02083.hp2 HG04115.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+1038_959+1044d others(9): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(2): Show |
A | 3 | a0001c0001t0001g0001 a0003c0003t0002g0051 a0005c0005t0002g0050 |
3 | HG01516.hp2 HG02027.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.959+1036_959+1044d others(11): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.959+1034_959+1044d others(13): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(6): Show |
A | 6 | a0001c0001t0001g0262 a0001c0001t0001g0273 a0002c0002t0002g0004 others(3): Show |
6 | HG00280.hp1 HG00609.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+1032_959+1044d others(15): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0298 a0002c0002t0002g0087 |
2 | NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.959+1030_959+1044d others(17): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(10): Show |
A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0263 a0001c0001t0001g0275 others(3): Show |
6 | HG00673.hp1 HG01243.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.959+1028_959+1044d others(19): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653030 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0325 a0001c0001t0001g0341 |
3 | HG03669.hp1 HG04184.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.959+1026_959+1044d others(21): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653030 | |||||||
| chr2:169653031 | T | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0284 a0001c0001t0001g0288 others(5): Show |
9 | HG01069.hp2 HG02109.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.959+1044A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653031 | |||||||
| chr2:169653032 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0025 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.959+1007_959+1042d others(38): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653032 | |||||||
| chr2:169653032 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.959+1006_959+1042d others(39): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653032 | |||||||
| chr2:169653033 | T | A | 23 | a0001c0001t0001g0022 a0001c0001t0001g0168 a0001c0001t0001g0174 others(20): Show |
23 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.959+1042A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653033 | |||||||
| chr2:169653035 | T | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(35): Show |
44 | HG00140.hp2 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.959+1040A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653035 | |||||||
| chr2:169653037 | T | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(38): Show |
49 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.959+1038A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653037 | |||||||
| chr2:169653039 | T | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(16): Show |
23 | HG00423.hp2 HG00673.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.959+1036A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653039 | |||||||
| chr2:169653041 | T | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(8): Show |
12 | HG00423.hp2 HG00673.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+1034A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653041 | |||||||
| chr2:169653043 | T | A | 11 | a0001c0001t0001g0142 a0001c0001t0001g0214 a0001c0001t0001g0268 others(8): Show |
13 | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.959+1032A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653043 | |||||||
| chr2:169653045 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.959+1030A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653045 | |||||||
| chr2:169653047 | T | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01123.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.959+1028A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653047 | |||||||
| chr2:169653049 | T | A | 10 | a0001c0001t0001g0247 a0001c0001t0001g0293 a0001c0001t0001g0299 others(7): Show |
10 | HG00323.hp2 HG00673.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+1026A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653049 | |||||||
| chr2:169653050 | A | G | 2 | a0006c0006t0002g0013 a0006c0006t0002g0100 |
3 | HG02258.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.959+1025T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653050 | |||||||
| chr2:169653052 | A | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.959+1023T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653052 | |||||||
| chr2:169653054 | ATATATAT others(7): Show |
A | 1 | a0002c0002t0002g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.959+1007_959+1020d others(16): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653054 | |||||||
| chr2:169653056 | A | G | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1019T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653056 | |||||||
| chr2:169653056 | ATATATAT others(5): Show |
A | 3 | a0002c0002t0002g0007 a0002c0002t0002g0083 a0002c0002t0002g0095 |
4 | HG03017.hp2 NA18981.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+1007_959+1018d others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653056 | |||||||
| chr2:169653064 | A | G | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+1011T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653064 | |||||||
| chr2:169653068 | G | A | 17 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(14): Show |
20 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.959+1007C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653068 | |||||||
| chr2:169653069 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.959+1006A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653069 | |||||||
| chr2:169653090 | G | GTA | 7 | a0001c0001t0001g0311 a0001c0001t0002g0101 a0001c0001t0002g0102 others(4): Show |
7 | HG02071.hp2 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+983_959+984dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653090 | |||||||
| chr2:169653098 | A | C | 10 | a0003c0003t0002g0011 a0003c0003t0002g0047 a0003c0003t0002g0051 others(7): Show |
11 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.959+977T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653098 | |||||||
| chr2:169653121 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.959+954G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653121 | |||||||
| chr2:169653127 | C | T | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+948G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653127 | |||||||
| chr2:169653165 | G | A | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.959+910C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653165 | |||||||
| chr2:169653263 | T | C | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+812A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653263 | |||||||
| chr2:169653399 | G | A | 1 | a0002c0002t0002g0094 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.959+676C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653399 | |||||||
| chr2:169653486 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(202): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.959+589T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653486 | |||||||
| chr2:169653536 | A | C | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+539T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653536 | |||||||
| chr2:169653563 | A | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.959+512T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653563 | |||||||
| chr2:169653599 | A | AT | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.959+475dupA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653599 | |||||||
| chr2:169653813 | A | G | 1 | a0002c0002t0002g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.959+262T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653813 | |||||||
| chr2:169653864 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.959+211G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653864 | |||||||
| chr2:169653918 | G | A | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.959+157C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653918 | |||||||
| chr2:169653919 | A | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02258.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.959+156T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 6/8 | chr2 | 169653919 | |||||||
| chr2:169654222 | G | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.820-8C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169654222 | |||||||
| chr2:169654516 | AATAAT | A | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-307_820-303del others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169654516 | |||||||
| chr2:169654717 | C | T | 10 | a0003c0003t0002g0011 a0003c0003t0002g0047 a0003c0003t0002g0051 others(7): Show |
11 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.820-503G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169654717 | |||||||
| chr2:169654871 | G | A | 3 | a0007c0009t0001g0236 a0007c0009t0001g0237 a0007c0009t0001g0238 |
3 | HG03209.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.820-657C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169654871 | |||||||
| chr2:169654959 | C | T | 1 | a0001c0008t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.820-745G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169654959 | |||||||
| chr2:169655049 | G | A | 27 | a0001c0001t0002g0096 a0001c0001t0002g0107 a0001c0001t0003g0097 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.820-835C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655049 | |||||||
| chr2:169655086 | T | A | 1 | a0001c0001t0003g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.820-872A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655086 | |||||||
| chr2:169655341 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.820-1127A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655341 | |||||||
| chr2:169655415 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1201A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655415 | |||||||
| chr2:169655435 | T | C | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-1221A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655435 | |||||||
| chr2:169655560 | T | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.820-1346A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655560 | |||||||
| chr2:169655602 | C | CA | 189 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(186): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.820-1389dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655602 | |||||||
| chr2:169655724 | C | T | 1 | a0008c0010t0001g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.820-1510G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655724 | |||||||
| chr2:169655832 | C | G | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-1618G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655832 | |||||||
| chr2:169655980 | G | A | 109 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(106): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.820-1766C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655980 | |||||||
| chr2:169655998 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.820-1784G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169655998 | |||||||
| chr2:169656164 | C | G | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.820-1950G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656164 | |||||||
| chr2:169656340 | A | G | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.820-2126T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656340 | |||||||
| chr2:169656366 | GAAGA | G | 36 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0102 others(33): Show |
37 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.820-2156_820-2153d others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656366 | |||||||
| chr2:169656368 | A | AGAG | 75 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.820-2155_820-2154i others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656368 | |||||||
| chr2:169656377 | A | AGG | 75 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.820-2164_820-2163i others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656377 | |||||||
| chr2:169656387 | A | AGGAGGAT others(5): Show |
57 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 others(54): Show |
68 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.820-2174_820-2173i others(14): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656387 | |||||||
| chr2:169656387 | A | AGGATGAA others(2): Show |
18 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(15): Show |
18 | HG00140.hp2 HG00558.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.820-2174_820-2173i others(11): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656387 | |||||||
| chr2:169656407 | G | T | 75 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.820-2193C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656407 | |||||||
| chr2:169656461 | AAGG | A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-2250_820-2248d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656461 | |||||||
| chr2:169656467 | G | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0275 a0001c0001t0001g0282 others(2): Show |
5 | NA18945.hp2 NA18961.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-2253C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656467 | |||||||
| chr2:169656498 | GGGA | G | 57 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0002g0096 others(54): Show |
63 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.820-2287_820-2285d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656498 | |||||||
| chr2:169656498 | GGGAGGA | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(53): Show |
62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.820-2290_820-2285d others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656498 | |||||||
| chr2:169656524 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-2310T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656524 | |||||||
| chr2:169656690 | G | A | 89 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(86): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.820-2476C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656690 | |||||||
| chr2:169656835 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.820-2621C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656835 | |||||||
| chr2:169656964 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(145): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.820-2751dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656964 | |||||||
| chr2:169656964 | C | CAA | 100 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.820-2752_820-2751d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656964 | |||||||
| chr2:169656964 | C | CAAA | 53 | a0001c0001t0001g0025 a0001c0001t0001g0139 a0001c0001t0001g0163 others(50): Show |
61 | HG00438.hp2 HG00733.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-2753_820-2751d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656964 | |||||||
| chr2:169656964 | C | CAAAA | 23 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(20): Show |
23 | HG00438.hp1 HG00621.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.820-2754_820-2751d others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656964 | |||||||
| chr2:169656988 | G | A | 1 | a0003c0003t0002g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.820-2774C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656988 | |||||||
| chr2:169656996 | TA | T | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.820-2783delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169656996 | |||||||
| chr2:169657096 | T | C | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-2882A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657096 | |||||||
| chr2:169657223 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.820-3009A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657223 | |||||||
| chr2:169657294 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.820-3080T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657294 | |||||||
| chr2:169657374 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.820-3160C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657374 | |||||||
| chr2:169657439 | T | C | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.820-3225A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657439 | |||||||
| chr2:169657610 | G | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-3396C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657610 | |||||||
| chr2:169657694 | AG | A | 27 | a0001c0001t0002g0096 a0001c0001t0002g0107 a0001c0001t0003g0097 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.820-3481delC | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657694 | |||||||
| chr2:169657713 | G | A | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-3499C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657713 | |||||||
| chr2:169657733 | A | C | 1 | a0015c0012t0001g0188 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.820-3519T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657733 | |||||||
| chr2:169657814 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.820-3600T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169657814 | |||||||
| chr2:169658304 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.819+3976A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658304 | |||||||
| chr2:169658367 | T | C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+3913A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658367 | |||||||
| chr2:169658448 | A | G | 22 | a0002c0002t0001g0323 a0002c0002t0002g0004 a0002c0002t0002g0007 others(19): Show |
27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.819+3832T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658448 | |||||||
| chr2:169658659 | A | G | 1 | a0002c0002t0002g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.819+3621T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658659 | |||||||
| chr2:169658726 | T | G | 102 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(99): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.819+3554A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658726 | |||||||
| chr2:169658963 | T | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+3317A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169658963 | |||||||
| chr2:169659027 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0302 a0001c0001t0001g0303 others(4): Show |
8 | NA18947.hp2 NA18964.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.819+3253C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659027 | |||||||
| chr2:169659049 | G | T | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+3231C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659049 | |||||||
| chr2:169659363 | G | A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+2917C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659363 | |||||||
| chr2:169659425 | A | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.819+2855T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659425 | |||||||
| chr2:169659439 | G | C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+2841C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659439 | |||||||
| chr2:169659782 | A | C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+2498T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169659782 | |||||||
| chr2:169660083 | TA | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
93 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.819+2196delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660083 | |||||||
| chr2:169660107 | G | T | 75 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.819+2173C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660107 | |||||||
| chr2:169660117 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.819+2163C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660117 | |||||||
| chr2:169660160 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.819+2120C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660160 | |||||||
| chr2:169660260 | C | T | 22 | a0002c0002t0001g0323 a0002c0002t0002g0004 a0002c0002t0002g0007 others(19): Show |
27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.819+2020G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660260 | |||||||
| chr2:169660421 | GT | G | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.819+1858delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660421 | |||||||
| chr2:169660518 | T | G | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.819+1762A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660518 | |||||||
| chr2:169660588 | T | TTA | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+1690_819+1691d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660588 | |||||||
| chr2:169660588 | TTA | T | 25 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(22): Show |
31 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.819+1690_819+1691d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660588 | |||||||
| chr2:169660592 | A | G | 22 | a0002c0002t0001g0323 a0002c0002t0002g0004 a0002c0002t0002g0007 others(19): Show |
27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.819+1688T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660592 | |||||||
| chr2:169660601 | TA | T | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+1678delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660601 | |||||||
| chr2:169660602 | A | AT | 3 | a0001c0001t0001g0025 a0001c0001t0001g0244 a0001c0001t0001g0297 |
4 | HG02559.hp2 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+1677dupA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660602 | |||||||
| chr2:169660602 | ATAT | A | 19 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(16): Show |
19 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.819+1675_819+1677d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660602 | |||||||
| chr2:169660603 | TA | T | 5 | a0001c0001t0001g0289 a0004c0004t0002g0068 a0007c0009t0001g0236 others(2): Show |
5 | HG02257.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+1676delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660603 | |||||||
| chr2:169660604 | A | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0025 others(18): Show |
23 | HG00323.hp1 HG00423.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.819+1676T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660604 | |||||||
| chr2:169660604 | AT | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
104 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.819+1675delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660604 | |||||||
| chr2:169660604 | ATT | A | 25 | a0001c0001t0002g0096 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
27 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.819+1674_819+1675d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660604 | |||||||
| chr2:169660604 | ATTT | A | 14 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0116 others(11): Show |
15 | HG00621.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.819+1673_819+1675d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660604 | |||||||
| chr2:169660605 | T | TA | 16 | a0001c0001t0001g0149 a0001c0001t0001g0164 a0001c0001t0001g0195 others(13): Show |
16 | HG02257.hp1 HG02630.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.819+1674_819+1675i others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660605 | |||||||
| chr2:169660606 | T | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0139 others(18): Show |
26 | HG00140.hp2 HG00735.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.819+1674A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660606 | |||||||
| chr2:169660607 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
89 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.819+1673A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660607 | |||||||
| chr2:169660608 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.819+1672A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660608 | |||||||
| chr2:169660609 | T | A | 3 | a0001c0001t0001g0336 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG00099.hp1 HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.819+1671A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660609 | |||||||
| chr2:169660801 | C | G | 1 | a0001c0001t0001g0318 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.819+1479G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660801 | |||||||
| chr2:169660822 | G | A | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.819+1458C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660822 | |||||||
| chr2:169660891 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.819+1389G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660891 | |||||||
| chr2:169660894 | C | T | 1 | a0003c0003t0002g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.819+1386G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660894 | |||||||
| chr2:169660896 | C | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
70 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.819+1384G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660896 | |||||||
| chr2:169660897 | C | T | 1 | a0002c0002t0002g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.819+1383G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660897 | |||||||
| chr2:169660936 | T | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
83 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.819+1344A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660936 | |||||||
| chr2:169660993 | A | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
92 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.819+1287T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169660993 | |||||||
| chr2:169661005 | T | C | 1 | a0001c0001t0003g0110 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.819+1275A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661005 | |||||||
| chr2:169661019 | C | A | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.819+1261G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661019 | |||||||
| chr2:169661081 | G | A | 18 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(15): Show |
18 | HG00140.hp2 HG00558.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.819+1199C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661081 | |||||||
| chr2:169661084 | C | T | 75 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(72): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.819+1196G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661084 | |||||||
| chr2:169661416 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.819+864G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661416 | |||||||
| chr2:169661438 | C | T | 111 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.819+842G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661438 | |||||||
| chr2:169661481 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.819+799C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661481 | |||||||
| chr2:169661492 | C | T | 31 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(28): Show |
33 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.819+788G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661492 | |||||||
| chr2:169661521 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.819+759G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661521 | |||||||
| chr2:169661538 | C | CATGCCCC others(9): Show |
1 | a0002c0002t0001g0323 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.819+741_819+742ins others(16): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661538 | |||||||
| chr2:169661852 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0008c0010t0001g0278 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+428T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661852 | |||||||
| chr2:169661880 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.819+400A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169661880 | |||||||
| chr2:169662023 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.819+257C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169662023 | |||||||
| chr2:169662079 | G | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+201C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 5/8 | chr2 | 169662079 | |||||||
| chr2:169662598 | C | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.663-162G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169662598 | |||||||
| chr2:169662786 | G | T | 1 | a0002c0002t0001g0323 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.663-350C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169662786 | |||||||
| chr2:169662859 | C | T | 27 | a0001c0001t0002g0096 a0001c0001t0002g0107 a0001c0001t0003g0097 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.663-423G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169662859 | |||||||
| chr2:169662917 | A | G | 1 | a0001c0007t0002g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.663-481T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169662917 | |||||||
| chr2:169662963 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(244): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.663-527G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169662963 | |||||||
| chr2:169663140 | A | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.663-704T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663140 | |||||||
| chr2:169663172 | C | T | 31 | a0001c0001t0001g0159 a0001c0001t0002g0029 a0001c0001t0002g0030 others(28): Show |
33 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.663-736G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663172 | |||||||
| chr2:169663211 | G | A | 3 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0090 |
3 | NA18993.hp2 NA19007.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.663-775C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663211 | |||||||
| chr2:169663273 | CT | C | 107 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(104): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.663-838delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663273 | |||||||
| chr2:169663280 | T | C | 1 | a0002c0002t0001g0323 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.663-844A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663280 | |||||||
| chr2:169663372 | A | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.663-936T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663372 | |||||||
| chr2:169663431 | A | G | 1 | a0002c0002t0001g0323 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.663-995T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663431 | |||||||
| chr2:169663477 | A | G | 101 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(98): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.663-1041T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663477 | |||||||
| chr2:169663515 | A | G | 8 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.663-1079T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663515 | |||||||
| chr2:169663548 | G | A | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.663-1112C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663548 | |||||||
| chr2:169663793 | T | TA | 18 | a0001c0001t0002g0042 a0003c0003t0002g0011 a0003c0003t0002g0047 others(15): Show |
20 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.663-1358dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663793 | |||||||
| chr2:169663796 | T | A | 55 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(52): Show |
62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.663-1360A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663796 | |||||||
| chr2:169663796 | T | TA | 27 | a0001c0001t0001g0143 a0001c0001t0001g0312 a0001c0001t0003g0097 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.663-1361dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663796 | |||||||
| chr2:169663799 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0275 |
2 | NA18964.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.663-1363T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663799 | |||||||
| chr2:169663806 | A | C | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.663-1370T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663806 | |||||||
| chr2:169663809 | C | A | 1 | a0002c0002t0002g0088 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.663-1373G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663809 | |||||||
| chr2:169663963 | C | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.663-1527G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169663963 | |||||||
| chr2:169664020 | C | G | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-1584G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664020 | |||||||
| chr2:169664026 | T | TA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.663-1591dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664026 | |||||||
| chr2:169664026 | TA | T | 15 | a0001c0001t0001g0158 a0001c0001t0001g0174 a0001c0001t0001g0183 others(12): Show |
15 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.663-1591delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664026 | |||||||
| chr2:169664201 | CA | C | 10 | a0003c0003t0002g0011 a0003c0003t0002g0047 a0003c0003t0002g0051 others(7): Show |
11 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.663-1766delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664201 | |||||||
| chr2:169664207 | A | T | 10 | a0003c0003t0002g0011 a0003c0003t0002g0047 a0003c0003t0002g0051 others(7): Show |
11 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.663-1771T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664207 | |||||||
| chr2:169664383 | A | G | 1 | a0002c0002t0002g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.663-1947T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664383 | |||||||
| chr2:169664390 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.663-1954G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664390 | |||||||
| chr2:169664504 | T | G | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.663-2068A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664504 | |||||||
| chr2:169664514 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.663-2078C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664514 | |||||||
| chr2:169664547 | T | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(37): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.663-2111A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664547 | |||||||
| chr2:169664888 | T | C | 5 | a0001c0001t0001g0266 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG01891.hp2 NA18906.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.663-2452A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664888 | |||||||
| chr2:169664892 | T | A | 2 | a0002c0002t0001g0323 a0002c0002t0002g0089 |
2 | HG00558.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.663-2456A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664892 | |||||||
| chr2:169664976 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.663-2540T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169664976 | |||||||
| chr2:169665164 | T | A | 3 | a0007c0009t0001g0236 a0007c0009t0001g0237 a0007c0009t0001g0238 |
3 | HG03209.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.663-2728A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665164 | |||||||
| chr2:169665307 | G | GA | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.663-2872dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665307 | |||||||
| chr2:169665430 | A | T | 1 | a0001c0001t0002g0032 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.663-2994T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665430 | |||||||
| chr2:169665476 | AT | A | 91 | a0001c0001t0001g0324 a0001c0001t0001g0329 a0001c0001t0002g0029 others(88): Show |
98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.663-3041delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665476 | |||||||
| chr2:169665534 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.663-3098A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665534 | |||||||
| chr2:169665638 | T | A | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.663-3202A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665638 | |||||||
| chr2:169665877 | C | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-3441G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169665877 | |||||||
| chr2:169666254 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0008c0010t0001g0278 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-3818T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666254 | |||||||
| chr2:169666286 | T | C | 14 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(11): Show |
14 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.663-3850A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666286 | |||||||
| chr2:169666637 | G | A | 14 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(11): Show |
14 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.663-4201C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666637 | |||||||
| chr2:169666708 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.663-4272G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666708 | |||||||
| chr2:169666709 | G | A | 1 | a0007c0009t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.663-4273C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666709 | |||||||
| chr2:169666713 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.663-4277A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666713 | |||||||
| chr2:169666777 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.663-4341G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666777 | |||||||
| chr2:169666919 | ATCCAT | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0008c0010t0001g0278 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-4488_663-4484d others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666919 | |||||||
| chr2:169666986 | A | T | 1 | a0001c0001t0002g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.663-4550T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169666986 | |||||||
| chr2:169667039 | G | C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.663-4603C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667039 | |||||||
| chr2:169667082 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.663-4646G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667082 | |||||||
| chr2:169667139 | TTTC | T | 108 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(105): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.663-4706_663-4704d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667139 | |||||||
| chr2:169667142 | C | CT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(45): Show |
55 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(52): Show |
intron_variant | MODIFIER | c.663-4707dupA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667142 | |||||||
| chr2:169667237 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.663-4801G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667237 | |||||||
| chr2:169667288 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663-4852C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667288 | |||||||
| chr2:169667391 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.663-4955C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667391 | |||||||
| chr2:169667618 | C | T | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(335): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.663-5182G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667618 | |||||||
| chr2:169667655 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.663-5219A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667655 | |||||||
| chr2:169667880 | T | C | 5 | a0003c0003t0002g0005 a0003c0003t0002g0058 a0003c0003t0002g0059 others(2): Show |
7 | HG01099.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.663-5444A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169667880 | |||||||
| chr2:169668130 | C | T | 4 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
4 | HG02145.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-5694G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668130 | |||||||
| chr2:169668181 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.663-5745T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668181 | |||||||
| chr2:169668325 | G | A | 1 | a0003c0003t0002g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.663-5889C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668325 | |||||||
| chr2:169668338 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.663-5902A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668338 | |||||||
| chr2:169668406 | G | C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.663-5970C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668406 | |||||||
| chr2:169668456 | T | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.663-6020A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668456 | |||||||
| chr2:169668573 | A | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+6003T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668573 | |||||||
| chr2:169668605 | T | C | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+5971A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668605 | |||||||
| chr2:169668651 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(88): Show |
107 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.662+5925C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668651 | |||||||
| chr2:169668661 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.662+5915C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668661 | |||||||
| chr2:169668800 | G | T | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.662+5776C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668800 | |||||||
| chr2:169668879 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.662+5697G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668879 | |||||||
| chr2:169668932 | C | A | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | HG02602.hp1 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.662+5644G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668932 | |||||||
| chr2:169668959 | T | C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.662+5617A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668959 | |||||||
| chr2:169668991 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.662+5585A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169668991 | |||||||
| chr2:169669022 | T | C | 4 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
4 | HG02145.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+5554A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669022 | |||||||
| chr2:169669090 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.662+5486A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669090 | |||||||
| chr2:169669201 | A | G | 89 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(86): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+5375T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669201 | |||||||
| chr2:169669206 | G | A | 13 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(10): Show |
13 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.662+5370C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669206 | |||||||
| chr2:169669247 | C | T | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+5329G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669247 | |||||||
| chr2:169669254 | G | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.662+5322C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669254 | |||||||
| chr2:169669292 | C | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+5284G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669292 | |||||||
| chr2:169669664 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.662+4912A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669664 | |||||||
| chr2:169669691 | T | G | 1 | a0001c0001t0002g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.662+4885A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669691 | |||||||
| chr2:169669711 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.662+4865G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669711 | |||||||
| chr2:169669766 | C | T | 1 | a0006c0006t0002g0013 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.662+4810G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669766 | |||||||
| chr2:169669774 | T | TA | 30 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0202 others(27): Show |
35 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.662+4801dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669774 | |||||||
| chr2:169669774 | TA | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(131): Show |
155 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.662+4801delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669774 | |||||||
| chr2:169669774 | TAAAAAAA | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.662+4795_662+4801d others(9): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669774 | |||||||
| chr2:169669823 | T | A | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.662+4753A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669823 | |||||||
| chr2:169669858 | A | G | 4 | a0004c0004t0002g0006 a0004c0004t0002g0068 a0004c0004t0002g0069 others(1): Show |
6 | HG01255.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.662+4718T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169669858 | |||||||
| chr2:169670186 | T | G | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+4390A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670186 | |||||||
| chr2:169670199 | T | C | 34 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(31): Show |
36 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.662+4377A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670199 | |||||||
| chr2:169670453 | A | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.662+4123T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670453 | |||||||
| chr2:169670495 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.662+4081T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670495 | |||||||
| chr2:169670781 | G | C | 9 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.662+3795C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670781 | |||||||
| chr2:169670804 | T | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
9 | HG02451.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+3772A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670804 | |||||||
| chr2:169670922 | C | A | 6 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0318 others(3): Show |
6 | HG00673.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+3654G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670922 | |||||||
| chr2:169670925 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+3651T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670925 | |||||||
| chr2:169670952 | T | C | 34 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(31): Show |
36 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.662+3624A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169670952 | |||||||
| chr2:169671054 | T | G | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+3522A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671054 | |||||||
| chr2:169671111 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.662+3465G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671111 | |||||||
| chr2:169671128 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.662+3448G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671128 | |||||||
| chr2:169671281 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+3295A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671281 | |||||||
| chr2:169671489 | A | T | 8 | a0004c0004t0002g0006 a0004c0004t0002g0068 a0004c0004t0002g0069 others(5): Show |
10 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.662+3087T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671489 | |||||||
| chr2:169671499 | G | A | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.662+3077C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671499 | |||||||
| chr2:169671647 | T | C | 36 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0102 others(33): Show |
37 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.662+2929A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671647 | |||||||
| chr2:169671693 | C | T | 1 | a0005c0005t0002g0050 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.662+2883G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671693 | |||||||
| chr2:169671740 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18954.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.662+2836C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671740 | |||||||
| chr2:169671740 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.662+2836C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671740 | |||||||
| chr2:169671771 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+2805C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671771 | |||||||
| chr2:169671906 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0171 |
2 | NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.662+2670G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671906 | |||||||
| chr2:169671981 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+2595A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169671981 | |||||||
| chr2:169672009 | G | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.662+2567C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672009 | |||||||
| chr2:169672177 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.662+2399A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672177 | |||||||
| chr2:169672271 | A | T | 8 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.662+2305T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672271 | |||||||
| chr2:169672410 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.662+2166G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672410 | |||||||
| chr2:169672456 | C | T | 1 | a0002c0002t0002g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.662+2120G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672456 | |||||||
| chr2:169672513 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662+2063A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672513 | |||||||
| chr2:169672580 | C | T | 2 | a0002c0002t0002g0081 a0002c0002t0002g0084 |
2 | NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.662+1996G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672580 | |||||||
| chr2:169672644 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+1932C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672644 | |||||||
| chr2:169672676 | G | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+1900C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672676 | |||||||
| chr2:169672853 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.662+1723G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672853 | |||||||
| chr2:169672958 | G | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
73 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.662+1618C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169672958 | |||||||
| chr2:169673009 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+1567C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673009 | |||||||
| chr2:169673068 | C | T | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.662+1508G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673068 | |||||||
| chr2:169673107 | C | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.662+1469G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673107 | |||||||
| chr2:169673149 | A | C | 1 | a0014c0015t0001g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.662+1427T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673149 | |||||||
| chr2:169673156 | G | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+1420C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673156 | |||||||
| chr2:169673219 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.662+1357G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673219 | |||||||
| chr2:169673319 | C | T | 1 | a0007c0009t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.662+1257G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673319 | |||||||
| chr2:169673499 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
5 | NA18941.hp2 NA18951.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.662+1077T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673499 | |||||||
| chr2:169673559 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+1017A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673559 | |||||||
| chr2:169673569 | A | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.662+1007T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673569 | |||||||
| chr2:169673605 | AG | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.662+970delC | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673605 | |||||||
| chr2:169673761 | G | A | 9 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0287 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.662+815C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673761 | |||||||
| chr2:169673773 | G | T | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.662+803C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673773 | |||||||
| chr2:169673814 | T | A | 5 | a0003c0003t0002g0011 a0003c0003t0002g0052 a0003c0003t0002g0053 others(2): Show |
6 | HG00280.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.662+762A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169673814 | |||||||
| chr2:169674016 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0275 a0001c0001t0001g0282 others(2): Show |
9 | NA18941.hp1 NA18960.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.662+560A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169674016 | |||||||
| chr2:169674080 | G | C | 19 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(16): Show |
23 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.662+496C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169674080 | |||||||
| chr2:169674234 | A | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.662+342T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169674234 | |||||||
| chr2:169674303 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.662+273G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 4/8 | chr2 | 169674303 | |||||||
| chr2:169675062 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-22A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675062 | |||||||
| chr2:169675104 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-64T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675104 | |||||||
| chr2:169675169 | A | AAT | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-131_295-130dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675169 | |||||||
| chr2:169675185 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-145A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675185 | |||||||
| chr2:169675203 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.295-163G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675203 | |||||||
| chr2:169675267 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295-227C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675267 | |||||||
| chr2:169675455 | G | A | 19 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(16): Show |
23 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-415C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675455 | |||||||
| chr2:169675509 | G | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-469C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675509 | |||||||
| chr2:169675574 | G | C | 1 | a0001c0001t0001g0305 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.295-534C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675574 | |||||||
| chr2:169675612 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.295-572A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675612 | |||||||
| chr2:169675690 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-650G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675690 | |||||||
| chr2:169675700 | A | C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-660T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675700 | |||||||
| chr2:169675760 | T | C | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.295-720A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675760 | |||||||
| chr2:169675923 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0261 |
2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.295-883G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675923 | |||||||
| chr2:169675965 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0218 |
2 | NA18961.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.295-925G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169675965 | |||||||
| chr2:169676238 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.295-1198C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676238 | |||||||
| chr2:169676366 | C | CA | 111 | a0001c0001t0001g0170 a0001c0001t0001g0205 a0001c0001t0002g0029 others(108): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.295-1327dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676366 | |||||||
| chr2:169676366 | CA | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0174 others(7): Show |
12 | HG00609.hp1 HG02723.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-1327delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676366 | |||||||
| chr2:169676420 | G | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-1380C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676420 | |||||||
| chr2:169676557 | CT | C | 109 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(106): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.295-1518delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676557 | |||||||
| chr2:169676558 | T | A | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.295-1518A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676558 | |||||||
| chr2:169676580 | C | T | 19 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(16): Show |
23 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-1540G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676580 | |||||||
| chr2:169676601 | T | C | 3 | a0001c0001t0003g0122 a0001c0001t0003g0125 a0001c0001t0003g0127 |
3 | HG01070.hp1 HG01071.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.295-1561A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676601 | |||||||
| chr2:169676610 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-1570A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676610 | |||||||
| chr2:169676881 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.295-1841A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676881 | |||||||
| chr2:169676935 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.295-1895A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169676935 | |||||||
| chr2:169677053 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-2013G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677053 | |||||||
| chr2:169677081 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
73 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.295-2041C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677081 | |||||||
| chr2:169677340 | A | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-2300T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677340 | |||||||
| chr2:169677391 | G | A | 9 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-2351C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677391 | |||||||
| chr2:169677563 | A | G | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.295-2523T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677563 | |||||||
| chr2:169677740 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.295-2700G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677740 | |||||||
| chr2:169677846 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0170 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.295-2806A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677846 | |||||||
| chr2:169677996 | G | A | 1 | a0004c0004t0002g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295-2956C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169677996 | |||||||
| chr2:169678106 | C | T | 2 | a0006c0006t0002g0013 a0006c0006t0002g0100 |
3 | HG02258.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.294+2901G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678106 | |||||||
| chr2:169678264 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(85): Show |
104 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.294+2743G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678264 | |||||||
| chr2:169678272 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.294+2735G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678272 | |||||||
| chr2:169678336 | T | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(244): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.294+2671A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678336 | |||||||
| chr2:169678337 | G | A | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.294+2670C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678337 | |||||||
| chr2:169678341 | C | CA | 11 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0151 others(8): Show |
11 | HG01978.hp1 HG02647.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.294+2665dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678341 | |||||||
| chr2:169678341 | CA | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0266 a0001c0001t0001g0271 others(3): Show |
6 | HG01169.hp1 HG01891.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+2665delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678341 | |||||||
| chr2:169678341 | CAAA | C | 55 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(52): Show |
57 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.294+2663_294+2665d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678341 | |||||||
| chr2:169678341 | CAAAA | C | 20 | a0001c0001t0002g0029 a0001c0001t0002g0096 a0001c0001t0002g0107 others(17): Show |
24 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.294+2662_294+2665d others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678341 | |||||||
| chr2:169678341 | CAAAAA | C | 10 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(7): Show |
11 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.294+2661_294+2665d others(7): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678341 | |||||||
| chr2:169678359 | A | AG | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.294+2647_294+2648i others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678359 | |||||||
| chr2:169678359 | A | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
89 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.294+2648T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678359 | |||||||
| chr2:169678402 | G | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.294+2605C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678402 | |||||||
| chr2:169678438 | T | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+2569A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678438 | |||||||
| chr2:169678680 | C | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.294+2327G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678680 | |||||||
| chr2:169678773 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+2234G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678773 | |||||||
| chr2:169678839 | T | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+2168A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678839 | |||||||
| chr2:169678840 | A | T | 31 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(28): Show |
33 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.294+2167T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678840 | |||||||
| chr2:169678884 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
18 | HG00438.hp2 HG02071.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.294+2123C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678884 | |||||||
| chr2:169678982 | G | C | 9 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+2025C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169678982 | |||||||
| chr2:169679009 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+1998T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679009 | |||||||
| chr2:169679038 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.294+1969A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679038 | |||||||
| chr2:169679148 | A | G | 8 | a0004c0004t0002g0006 a0004c0004t0002g0068 a0004c0004t0002g0069 others(5): Show |
10 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.294+1859T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679148 | |||||||
| chr2:169679160 | T | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(244): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.294+1847A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679160 | |||||||
| chr2:169679173 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+1834G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679173 | |||||||
| chr2:169679230 | C | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
9 | HG02451.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+1777G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679230 | |||||||
| chr2:169679371 | C | T | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.294+1636G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679371 | |||||||
| chr2:169679406 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.294+1601C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679406 | |||||||
| chr2:169679445 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.294+1562C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679445 | |||||||
| chr2:169679452 | G | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.294+1555C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679452 | |||||||
| chr2:169679488 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.294+1519G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679488 | |||||||
| chr2:169679550 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.294+1457T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679550 | |||||||
| chr2:169679594 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.294+1413A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679594 | |||||||
| chr2:169679597 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+1410G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679597 | |||||||
| chr2:169679630 | G | A | 1 | a0006c0006t0002g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.294+1377C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679630 | |||||||
| chr2:169679680 | C | CA | 84 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.294+1326dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679680 | |||||||
| chr2:169679680 | C | CAA | 95 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(92): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.294+1325_294+1326d others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679680 | |||||||
| chr2:169679680 | C | CAAA | 43 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(40): Show |
44 | HG00438.hp1 HG00621.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.294+1324_294+1326d others(5): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679680 | |||||||
| chr2:169679680 | CA | C | 7 | a0001c0001t0001g0173 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG01169.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+1326delT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679680 | |||||||
| chr2:169679702 | A | AC | 3 | a0005c0005t0002g0012 a0005c0005t0002g0048 a0005c0005t0002g0049 |
4 | HG00323.hp1 HG02698.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1304_294+1305i others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679702 | |||||||
| chr2:169679813 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.294+1194A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679813 | |||||||
| chr2:169679907 | T | C | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.294+1100A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679907 | |||||||
| chr2:169679941 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.294+1066A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169679941 | |||||||
| chr2:169680063 | C | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+944G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680063 | |||||||
| chr2:169680071 | C | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+936G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680071 | |||||||
| chr2:169680128 | T | C | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.294+879A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680128 | |||||||
| chr2:169680133 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+874T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680133 | |||||||
| chr2:169680219 | T | G | 1 | a0005c0005t0002g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.294+788A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680219 | |||||||
| chr2:169680255 | C | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+752G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680255 | |||||||
| chr2:169680364 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+643A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680364 | |||||||
| chr2:169680390 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.294+617A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680390 | |||||||
| chr2:169680429 | T | A | 1 | a0003c0003t0002g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.294+578A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680429 | |||||||
| chr2:169680450 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+557C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680450 | |||||||
| chr2:169680518 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.294+489A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680518 | |||||||
| chr2:169680793 | G | A | 19 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(16): Show |
23 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+214C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680793 | |||||||
| chr2:169680892 | G | A | 22 | a0001c0001t0001g0266 a0002c0002t0002g0004 a0002c0002t0002g0007 others(19): Show |
27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.294+115C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 2/8 | chr2 | 169680892 | |||||||
| chr2:169681412 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02976.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68-179C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169681412 | |||||||
| chr2:169681639 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.68-406A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169681639 | |||||||
| chr2:169681880 | AAGAC | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-651_68-648delGT others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169681880 | |||||||
| chr2:169681909 | T | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-676A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169681909 | |||||||
| chr2:169682083 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-850C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682083 | |||||||
| chr2:169682092 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.68-859C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682092 | |||||||
| chr2:169682210 | TCTAA | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.68-981_68-978delTT others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682210 | |||||||
| chr2:169682270 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
76 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.68-1037G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682270 | |||||||
| chr2:169682485 | T | TAC | 54 | a0001c0001t0001g0171 a0001c0001t0002g0029 a0001c0001t0002g0030 others(51): Show |
60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.68-1254_68-1253dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682485 | |||||||
| chr2:169682539 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68-1306C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682539 | |||||||
| chr2:169682648 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-1415C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682648 | |||||||
| chr2:169682682 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.68-1449A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682682 | |||||||
| chr2:169682895 | A | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02258.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1662T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682895 | |||||||
| chr2:169682902 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-1669C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682902 | |||||||
| chr2:169682922 | G | A | 9 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-1689C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169682922 | |||||||
| chr2:169683028 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-1795G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683028 | |||||||
| chr2:169683170 | T | G | 1 | a0001c0008t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.68-1937A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683170 | |||||||
| chr2:169683195 | C | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | NA18612.hp2 NA19000.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.68-1962G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683195 | |||||||
| chr2:169683270 | G | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
84 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.68-2037C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683270 | |||||||
| chr2:169683304 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-2071C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683304 | |||||||
| chr2:169683703 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.68-2470G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683703 | |||||||
| chr2:169683703 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.68-2470G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683703 | |||||||
| chr2:169683980 | G | A | 4 | a0001c0001t0003g0115 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG00438.hp1 HG00621.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-2747C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169683980 | |||||||
| chr2:169684327 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-3094G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684327 | |||||||
| chr2:169684340 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-3107C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684340 | |||||||
| chr2:169684365 | G | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02258.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-3132C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684365 | |||||||
| chr2:169684378 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-3145G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684378 | |||||||
| chr2:169684545 | G | A | 1 | a0003c0003t0002g0057 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-3312C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684545 | |||||||
| chr2:169684628 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-3395T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684628 | |||||||
| chr2:169684636 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.68-3403A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684636 | |||||||
| chr2:169684648 | C | CGTT | 30 | a0001c0001t0001g0172 a0001c0001t0001g0252 a0001c0001t0001g0255 others(27): Show |
30 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-3418_68-3416dup others(3): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684648 | |||||||
| chr2:169684648 | CGTTGTT | C | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.68-3421_68-3416del others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684648 | |||||||
| chr2:169684747 | G | A | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.68-3514C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684747 | |||||||
| chr2:169684900 | C | A | 1 | a0004c0004t0002g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-3667G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169684900 | |||||||
| chr2:169685005 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-3772T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685005 | |||||||
| chr2:169685112 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-3879T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685112 | |||||||
| chr2:169685151 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0008c0010t0001g0278 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3918T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685151 | |||||||
| chr2:169685235 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-4002G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685235 | |||||||
| chr2:169685257 | T | A | 1 | a0001c0001t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.68-4024A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685257 | |||||||
| chr2:169685324 | C | T | 8 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-4091G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685324 | |||||||
| chr2:169685374 | A | T | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.68-4141T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685374 | |||||||
| chr2:169685569 | G | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0107 |
2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.68-4336C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685569 | |||||||
| chr2:169685599 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.68-4366C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685599 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2518): Show |
1 | a0001c0001t0003g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2525): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2517): Show |
1 | a0001c0001t0003g0110 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2524): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2519): Show |
1 | a0001c0001t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2526): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2338): Show |
1 | a0001c0001t0003g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2345): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2337): Show |
2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2344): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2516): Show |
2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2523): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2517): Show |
2 | a0001c0001t0003g0124 a0001c0001t0003g0125 |
2 | HG01070.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2524): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2516): Show |
2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2523): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2515): Show |
5 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(2): Show |
5 | HG00733.hp1 HG02523.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2522): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2516): Show |
6 | a0001c0001t0003g0097 a0001c0001t0003g0120 a0001c0001t0003g0121 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4474_68-4473ins others(2523): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2516): Show |
1 | a0001c0001t0003g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2523): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685706 | T | TAAGTTTT others(2467): Show |
1 | a0001c0001t0003g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.68-4474_68-4473ins others(2474): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685706 | |||||||
| chr2:169685738 | C | T | 36 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0102 others(33): Show |
37 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.68-4505G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685738 | |||||||
| chr2:169685852 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-4619T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169685852 | |||||||
| chr2:169686104 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-4871C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686104 | |||||||
| chr2:169686112 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0297 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.68-4879C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686112 | |||||||
| chr2:169686190 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-4957C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686190 | |||||||
| chr2:169686225 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.68-4992C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686225 | |||||||
| chr2:169686279 | CTATTGTC others(2): Show |
C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-5055_68-5047del others(9): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686279 | |||||||
| chr2:169686354 | G | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18978.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.68-5121C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686354 | |||||||
| chr2:169686438 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-5205G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686438 | |||||||
| chr2:169686593 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
73 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.68-5360C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686593 | |||||||
| chr2:169686616 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-5383T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686616 | |||||||
| chr2:169686785 | C | G | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0014c0015t0001g0292 |
3 | HG00673.hp1 NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.68-5552G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686785 | |||||||
| chr2:169686958 | G | A | 5 | a0003c0003t0002g0005 a0003c0003t0002g0058 a0003c0003t0002g0059 others(2): Show |
7 | HG01099.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-5725C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686958 | |||||||
| chr2:169686980 | C | T | 12 | a0004c0004t0002g0006 a0004c0004t0002g0061 a0004c0004t0002g0067 others(9): Show |
14 | HG00733.hp2 HG01255.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-5747G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686980 | |||||||
| chr2:169686981 | A | G | 123 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(120): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.68-5748T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686981 | |||||||
| chr2:169686986 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0213 |
4 | NA18980.hp2 NA19056.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-5753C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686986 | |||||||
| chr2:169686998 | T | C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-5765A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169686998 | |||||||
| chr2:169687010 | C | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0022 others(150): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.68-5777G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687010 | |||||||
| chr2:169687150 | G | A | 5 | a0002c0002t0002g0081 a0002c0002t0002g0082 a0002c0002t0002g0083 others(2): Show |
5 | HG00621.hp2 HG03017.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-5917C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687150 | |||||||
| chr2:169687205 | A | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-5972T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687205 | |||||||
| chr2:169687210 | A | G | 2 | a0001c0001t0003g0109 a0001c0001t0003g0110 |
2 | NA18946.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.68-5977T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687210 | |||||||
| chr2:169687282 | G | A | 1 | a0006c0006t0002g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-6049C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687282 | |||||||
| chr2:169687325 | C | T | 1 | a0006c0006t0002g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-6092G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687325 | |||||||
| chr2:169687490 | C | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0044 |
3 | HG00735.hp2 HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.68-6257G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687490 | |||||||
| chr2:169687494 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.68-6261C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687494 | |||||||
| chr2:169687514 | G | GAC | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-6282_68-6281ins others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687514 | |||||||
| chr2:169687574 | T | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(335): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.68-6341A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687574 | |||||||
| chr2:169687602 | T | C | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.68-6369A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687602 | |||||||
| chr2:169687627 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68-6394G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687627 | |||||||
| chr2:169687860 | CTGCCTCT others(12): Show |
C | 36 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0102 others(33): Show |
37 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+6382_67+6400del others(19): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687860 | |||||||
| chr2:169687865 | T | A | 19 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(16): Show |
23 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.67+6396A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687865 | |||||||
| chr2:169687959 | C | T | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.67+6302G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169687959 | |||||||
| chr2:169688114 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.67+6147G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688114 | |||||||
| chr2:169688320 | G | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.67+5941C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688320 | |||||||
| chr2:169688331 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67+5930T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688331 | |||||||
| chr2:169688374 | T | A | 3 | a0006c0006t0002g0013 a0006c0006t0002g0099 a0006c0006t0002g0100 |
4 | HG02258.hp1 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5887A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688374 | |||||||
| chr2:169688448 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+5813T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688448 | |||||||
| chr2:169688490 | A | C | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+5771T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688490 | |||||||
| chr2:169688527 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+5734A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688527 | |||||||
| chr2:169688565 | C | G | 8 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+5696G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688565 | |||||||
| chr2:169688575 | A | C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+5686T>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688575 | |||||||
| chr2:169688847 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+5414T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688847 | |||||||
| chr2:169688855 | A | G | 2 | a0006c0006t0002g0013 a0006c0006t0002g0100 |
3 | HG02258.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.67+5406T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688855 | |||||||
| chr2:169688887 | C | T | 4 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
4 | HG02145.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5374G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688887 | |||||||
| chr2:169688923 | C | T | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0008c0010t0001g0278 others(1): Show |
4 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5338G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688923 | |||||||
| chr2:169688987 | T | C | 2 | a0006c0006t0002g0013 a0006c0006t0002g0100 |
3 | HG02258.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.67+5274A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169688987 | |||||||
| chr2:169689111 | G | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+5150C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689111 | |||||||
| chr2:169689161 | T | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+5100A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689161 | |||||||
| chr2:169689187 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67+5074T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689187 | |||||||
| chr2:169689316 | G | C | 1 | a0011c0014t0003g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.67+4945C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689316 | |||||||
| chr2:169689390 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.67+4871A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689390 | |||||||
| chr2:169689466 | T | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67+4795A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689466 | |||||||
| chr2:169689479 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.67+4782G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689479 | |||||||
| chr2:169689661 | C | T | 20 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(17): Show |
24 | HG00280.hp1 HG00323.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.67+4600G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689661 | |||||||
| chr2:169689735 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+4526G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689735 | |||||||
| chr2:169689747 | C | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG00558.hp1 NA18997.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.67+4514G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689747 | |||||||
| chr2:169689953 | A | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(50): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.67+4308T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169689953 | |||||||
| chr2:169690069 | T | G | 4 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
4 | HG02145.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4192A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690069 | |||||||
| chr2:169690160 | C | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4101G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690160 | |||||||
| chr2:169690163 | G | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4098C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690163 | |||||||
| chr2:169690166 | C | G | 109 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(106): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.67+4095G>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690166 | |||||||
| chr2:169690169 | G | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4092C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690169 | |||||||
| chr2:169690178 | C | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4083G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690178 | |||||||
| chr2:169690182 | G | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4079C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690182 | |||||||
| chr2:169690185 | G | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4076C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690185 | |||||||
| chr2:169690186 | A | G | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4075T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690186 | |||||||
| chr2:169690203 | A | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4058T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690203 | |||||||
| chr2:169690204 | T | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4057A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690204 | |||||||
| chr2:169690226 | A | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4035T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690226 | |||||||
| chr2:169690227 | G | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4034C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690227 | |||||||
| chr2:169690240 | A | T | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4021T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690240 | |||||||
| chr2:169690244 | T | A | 1 | a0004c0004t0002g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+4017A>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690244 | |||||||
| chr2:169690276 | C | T | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+3985G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690276 | |||||||
| chr2:169690329 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.67+3932C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690329 | |||||||
| chr2:169690450 | G | A | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+3811C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690450 | |||||||
| chr2:169690612 | G | A | 2 | a0002c0002t0002g0094 a0004c0004t0002g0061 |
2 | HG02896.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.67+3649C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690612 | |||||||
| chr2:169690663 | C | CA | 99 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+3597dupT | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690663 | |||||||
| chr2:169690663 | C | CAA | 11 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0285 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+3596_67+3597dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690663 | |||||||
| chr2:169690685 | C | A | 1 | a0006c0006t0002g0013 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.67+3576G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690685 | |||||||
| chr2:169690856 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.67+3405G>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690856 | |||||||
| chr2:169690928 | G | T | 3 | a0001c0007t0002g0064 a0001c0007t0002g0065 a0001c0007t0002g0066 |
3 | HG01496.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.67+3333C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690928 | |||||||
| chr2:169690963 | G | C | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.67+3298C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690963 | |||||||
| chr2:169690994 | T | C | 9 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3267A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169690994 | |||||||
| chr2:169691236 | A | T | 36 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0102 others(33): Show |
37 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+3025T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691236 | |||||||
| chr2:169691292 | T | C | 6 | a0001c0001t0001g0144 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG02257.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2969A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691292 | |||||||
| chr2:169691389 | C | T | 1 | a0012c0013t0002g0076 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+2872G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691389 | |||||||
| chr2:169691442 | C | T | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0280 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2819G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691442 | |||||||
| chr2:169691461 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+2800C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691461 | |||||||
| chr2:169691723 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.67+2538C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169691723 | |||||||
| chr2:169692169 | A | G | 1 | a0006c0006t0002g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+2092T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692169 | |||||||
| chr2:169692261 | T | C | 25 | a0001c0001t0003g0097 a0001c0001t0003g0109 a0001c0001t0003g0110 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+2000A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692261 | |||||||
| chr2:169692442 | A | ACG | 4 | a0001c0001t0001g0003 a0001c0001t0001g0275 a0001c0001t0001g0282 others(1): Show |
8 | NA18941.hp1 NA18960.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+1817_67+1818dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692442 | |||||||
| chr2:169692442 | A | ACGCG | 18 | a0001c0001t0003g0109 a0001c0001t0003g0110 a0001c0001t0003g0111 others(15): Show |
18 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+1818_67+1819ins others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692442 | |||||||
| chr2:169692442 | ACG | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01884.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1817_67+1818del others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692442 | |||||||
| chr2:169692444 | G | GCA | 34 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
38 | HG00558.hp2 HG00609.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+1815_67+1816dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCACA | 12 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(9): Show |
12 | HG00099.hp2 HG01192.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+1813_67+1816dup others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCACACA | 3 | a0001c0001t0001g0255 a0002c0002t0002g0007 a0002c0002t0002g0095 |
5 | HG04184.hp2 NA18981.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1811_67+1816dup others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCACACAC others(1): Show |
6 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0001t0001g0268 others(3): Show |
6 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+1809_67+1816dup others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67+1805_67+1816dup others(12): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCGCA | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG03704.hp1 NA18939.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1816_67+1817ins others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCGCACA | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0026 others(42): Show |
52 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.67+1816_67+1817ins others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCGCACAC others(1): Show |
7 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 others(4): Show |
7 | HG00099.hp1 HG01433.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+1816_67+1817ins others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCGCACAC others(3): Show |
3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 |
3 | HG03017.hp1 HG03942.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.67+1816_67+1817ins others(10): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | G | GCGCGCA | 7 | a0001c0001t0003g0097 a0001c0001t0003g0126 a0001c0001t0003g0127 others(4): Show |
7 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+1816_67+1817ins others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | GCA | G | 13 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(10): Show |
13 | HG01358.hp1 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+1815_67+1816del others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | GCACA | G | 34 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(31): Show |
36 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.67+1813_67+1816del others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | GCACACA | G | 24 | a0001c0001t0002g0096 a0001c0001t0002g0107 a0001c0007t0002g0064 others(21): Show |
28 | HG00280.hp1 HG00323.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.67+1811_67+1816del others(6): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692444 | GCACACAC others(1): Show |
G | 4 | a0004c0004t0002g0061 a0006c0006t0002g0013 a0006c0006t0002g0099 others(1): Show |
5 | HG02258.hp1 HG02896.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1809_67+1816del others(8): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692444 | |||||||
| chr2:169692446 | A | G | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02976.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.67+1815T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692446 | |||||||
| chr2:169692448 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67+1813T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692448 | |||||||
| chr2:169692450 | A | G | 3 | a0001c0001t0002g0032 a0003c0003t0002g0062 a0003c0003t0002g0063 |
3 | HG01099.hp1 HG04228.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.67+1811T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692450 | |||||||
| chr2:169692452 | A | G | 17 | a0003c0003t0002g0005 a0003c0003t0002g0011 a0003c0003t0002g0047 others(14): Show |
21 | HG00280.hp1 HG00323.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.67+1809T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692452 | |||||||
| chr2:169692492 | C | CAG | 13 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG02145.hp1 HG02258.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+1767_67+1768dup others(2): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692492 | |||||||
| chr2:169692561 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.67+1700A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692561 | |||||||
| chr2:169692625 | AT | A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA18906.hp2 NA19030.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1635delA | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692625 | |||||||
| chr2:169692670 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 |
3 | HG02976.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.67+1591C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692670 | |||||||
| chr2:169692686 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.67+1575G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692686 | |||||||
| chr2:169692765 | A | T | 1 | a0011c0014t0003g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.67+1496T>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692765 | |||||||
| chr2:169692777 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+1484T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692777 | |||||||
| chr2:169692942 | A | G | 3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 |
3 | HG00140.hp2 HG01256.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.67+1319T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692942 | |||||||
| chr2:169692988 | C | T | 13 | a0001c0001t0001g0139 a0001c0001t0001g0266 a0001c0001t0001g0267 others(10): Show |
13 | HG01891.hp2 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.67+1273G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169692988 | |||||||
| chr2:169693051 | G | T | 1 | a0001c0001t0003g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+1210C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693051 | |||||||
| chr2:169693089 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.67+1172C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693089 | |||||||
| chr2:169693103 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.67+1158C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693103 | |||||||
| chr2:169693188 | A | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG01123.hp1 HG01243.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.67+1073T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693188 | |||||||
| chr2:169693249 | G | A | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+1012C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693249 | |||||||
| chr2:169693340 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02132.hp2 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+921T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693340 | |||||||
| chr2:169693551 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67+710A>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693551 | |||||||
| chr2:169693555 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+706G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693555 | |||||||
| chr2:169693645 | G | C | 21 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0077 others(18): Show |
26 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+616C>G | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693645 | |||||||
| chr2:169693707 | C | T | 74 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(71): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.67+554G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693707 | |||||||
| chr2:169693708 | A | G | 110 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(107): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+553T>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693708 | |||||||
| chr2:169693740 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+521A>C | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693740 | |||||||
| chr2:169693871 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67+390G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693871 | |||||||
| chr2:169693948 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67+313C>T | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693948 | |||||||
| chr2:169693972 | AGCTGGG | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.67+283_67+288delCC others(4): Show |
CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169693972 | |||||||
| chr2:169694117 | C | T | 4 | a0001c0001t0001g0139 a0001c0008t0001g0136 a0001c0008t0001g0137 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+144G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169694117 | |||||||
| chr2:169694207 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
5 | NA18941.hp2 NA18951.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+54G>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169694207 | |||||||
| chr2:169694217 | G | T | 18 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(15): Show |
18 | HG00140.hp2 HG00558.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+44C>A | CFAP210 | ENSG00000154479.13 | transcript | ENST00000447353.6 | protein_coding | 1/8 | chr2 | 169694217 |