Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90799 |
| ensemblid | ENSG00000258890.8 |
| hgncid | 25141 |
| symbol | CEP95 |
| name | centrosomal protein 95 |
| refseq_nuc | NM_138363.3 |
| refseq_prot | NP_612372.1 |
| ensembl_nuc | ENST00000556440.7 |
| ensembl_prot | ENSP00000450461.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 64506977 |
| end | 64537946 |
| strand | + |
| ver | v1.2 |
| region | chr17:64506977-64537946 |
| region5000 | chr17:64501977-64542946 |
| regionname0 | CEP95_chr17_64506977_64537946 |
| regionname5000 | CEP95_chr17_64501977_64542946 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 821 | 238 | 81 | 44 | 73 | 7 | 31 | 54 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0002 | 0/0 | 821 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0003 | 0/0 | 821 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0004 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0005 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0006 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0007 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0008 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0009 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| a0010 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | MAGSD others(816): Show |
chr17 | 64501977 | 64542946 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2463 | 237 | 81 | 44 | 72 | 7 | 31 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0001c0009 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0002c0002 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0003c0008 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0004c0004 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0005c0005 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0006c0003 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0007c0007 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0008c0011 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0009c0010 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 | ||
| a0010c0006 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | ATGGC others(2458): Show |
chr17 | 64501977 | 64542946 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2754 | 132 | 13 | 27 | 61 | 4 | 25 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0001c0001t0002 | 0/0 | 2754 | 102 | 67 | 15 | 11 | 3 | 6 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0001c0001t0003 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0001c0001t0004 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0001c0009t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0002c0002t0002 | 0/0 | 2754 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0003c0008t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0004c0004t0002 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0005c0005t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0006c0003t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0007c0007t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0008c0011t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0009c0010t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| a0010c0006t0001 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | CTTCC others(2749): Show |
chr17 | 64501977 | 64542946 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 5 | 7 | 14 | 1 | 3 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 2 | 3 | 0 | 5 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0002 | 0/0 | 11 | 0 | 1 | 8 | 0 | 2 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0005 | 0/0 | 6 | 2 | 1 | 0 | 0 | 3 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0001c0009t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0003c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0004c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0005c0005t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0006c0003t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0007c0007t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0008c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0009c0010t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| a0010c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01517 | hp2 | a0003 | c0008 | t0001 | g0077 | EUR | IBS | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02129 | hp2 | a0004 | c0004 | t0002 | g0054 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02630 | hp2 | a0005 | c0005 | t0002 | g0119 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02723 | hp2 | a0006 | c0003 | t0002 | g0134 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03453 | hp2 | a0007 | c0007 | t0002 | g0043 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03654 | hp2 | a0008 | c0011 | t0001 | g0001 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03834 | hp1 | a0009 | c0010 | t0001 | g0011 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03834 | hp2 | a0010 | c0006 | t0001 | g0101 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18973 | hp2 | a0001 | c0009 | t0001 | g0026 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ASW | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | USA | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0115 | REF | REF | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0113 | REF | REF | CEP95_chr17_64501977_64542946 | CEP95 | chr17 | 64501977 | 64542946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:64519342 | G | A | 1 | a0006 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.495G>A | p.Met165Ile | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/20 | 616/2754 | 495/2466 | 165/821 | chr17 | 64519342 | |||
| chr17:64522809 | C | T | 1 | a0008 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.823C>T | p.Pro275Ser | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/20 | 944/2754 | 823/2466 | 275/821 | chr17 | 64522809 | |||
| chr17:64526195 | G | A | 1 | a0004 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1147G>A | p.Asp383Asn | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/20 | 1268/2754 | 1147/2466 | 383/821 | chr17 | 64526195 | |||
| chr17:64529353 | C | T | 1 | a0009 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1372C>T | p.His458Tyr | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/20 | 1493/2754 | 1372/2466 | 458/821 | chr17 | 64529353 | |||
| chr17:64534646 | G | A | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1979G>A | p.Arg660Gln | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/20 | 2100/2754 | 1979/2466 | 660/821 | chr17 | 64534646 | |||
| chr17:64534675 | T | G | 1 | a0002 | 2 | HG02258.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2008T>G | p.Tyr670Asp | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/20 | 2129/2754 | 2008/2466 | 670/821 | chr17 | 64534675 | |||
| chr17:64536719 | G | A | 1 | a0010 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2188G>A | p.Asp730Asn | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 18/20 | 2309/2754 | 2188/2466 | 730/821 | chr17 | 64536719 | |||
| chr17:64537729 | T | C | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2416T>C | p.Ser806Pro | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 2537/2754 | 2416/2466 | 806/821 | chr17 | 64537729 | |||
| chr17:64537772 | C | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.2459C>T | p.Ser820Phe | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 2580/2754 | 2459/2466 | 820/821 | chr17 | 64537772 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:64533122 | A | G | 1 | a0001c0009 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.1848A>G | p.Glu616Glu | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/20 | 1969/2754 | 1848/2466 | 616/821 | chr17 | 64533122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:64507013 | T | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
111 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-85T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/20 | 85 | chr17 | 64507013 | ||||||
| chr17:64507093 | G | A | 1 | a0001c0001t0004 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-5G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/20 | 5 | chr17 | 64507093 | ||||||
| chr17:64537905 | A | G | 1 | a0001c0001t0003 | 2 | HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*126A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 20/20 | 126 | chr17 | 64537905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:64507365 | C | T | 3 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0002g0141 |
3 | HG03139.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19+249C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507365 | |||||||
| chr17:64507412 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG01175.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19+296T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507412 | |||||||
| chr17:64507414 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19+298T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507414 | |||||||
| chr17:64507480 | GCTTTTGT others(6): Show |
G | 1 | a0001c0001t0002g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19+369_19+381delTG others(11): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr17 | 64507480 | ||||||
| chr17:64507570 | C | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+454C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507570 | |||||||
| chr17:64507766 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.19+650G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507766 | |||||||
| chr17:64507809 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+693T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507809 | |||||||
| chr17:64507845 | C | G | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19+729C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507845 | |||||||
| chr17:64507917 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0133 |
6 | HG01109.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-675C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64507917 | |||||||
| chr17:64508115 | G | A | 9 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(6): Show |
19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.20-477G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508115 | |||||||
| chr17:64508217 | C | G | 20 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0030 others(17): Show |
32 | HG01175.hp1 HG01243.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-375C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508217 | |||||||
| chr17:64508234 | GTTGT | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-355_20-352delGT others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr17 | 64508234 | ||||||
| chr17:64508351 | C | G | 20 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0030 others(17): Show |
32 | HG01175.hp1 HG01243.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-241C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 1/19 | chr17 | 64508351 | |||||||
| chr17:64508866 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.148+146A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508866 | |||||||
| chr17:64508872 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0040 others(3): Show |
15 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.148+152C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508872 | |||||||
| chr17:64508916 | C | T | 3 | a0001c0001t0002g0132 a0002c0002t0002g0130 a0002c0002t0002g0131 |
3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.148+196C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508916 | |||||||
| chr17:64508955 | C | G | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148+235C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508955 | |||||||
| chr17:64508956 | C | T | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148+236C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64508956 | |||||||
| chr17:64509040 | C | A | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(44): Show |
80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.148+320C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509040 | |||||||
| chr17:64509222 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.148+502T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509222 | |||||||
| chr17:64509319 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.148+599A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509319 | |||||||
| chr17:64509402 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(4): Show |
11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+682C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509402 | |||||||
| chr17:64509405 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0019 others(6): Show |
15 | HG00438.hp1 HG00544.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.148+685G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509405 | |||||||
| chr17:64509514 | A | G | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149-659A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509514 | |||||||
| chr17:64509762 | G | A | 1 | a0007c0007t0002g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.149-411G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509762 | |||||||
| chr17:64509818 | A | G | 1 | a0004c0004t0002g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.149-355A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509818 | |||||||
| chr17:64509871 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.149-302T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509871 | |||||||
| chr17:64509881 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-292G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509881 | |||||||
| chr17:64509905 | C | CTA | 12 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(9): Show |
14 | HG00639.hp1 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-254_149-253dup others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr17 | 64509905 | ||||||
| chr17:64509960 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149-213T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509960 | |||||||
| chr17:64509970 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0121 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.149-203G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64509970 | |||||||
| chr17:64510156 | A | AT | 9 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(6): Show |
13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.149-11dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr17 | 64510156 | ||||||
| chr17:64510162 | T | C | 33 | a0001c0001t0001g0065 a0001c0001t0002g0002 a0001c0001t0002g0004 others(30): Show |
61 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.149-11T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64510162 | |||||||
| chr17:64510169 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.149-4C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 2/19 | chr17 | 64510169 | |||||||
| chr17:64510305 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.256+25T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510305 | |||||||
| chr17:64510629 | A | G | 9 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(6): Show |
19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.256+349A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510629 | |||||||
| chr17:64510671 | TC | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0053 |
3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.256+394delC | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr17 | 64510671 | ||||||
| chr17:64510682 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0121 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.256+402C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510682 | |||||||
| chr17:64510705 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0129 |
4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+425A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510705 | |||||||
| chr17:64510725 | A | G | 1 | a0001c0001t0001g0029 | 2 | NA18997.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.256+445A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510725 | |||||||
| chr17:64510908 | G | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(7): Show |
26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.256+628G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510908 | |||||||
| chr17:64510968 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.256+688G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64510968 | |||||||
| chr17:64511303 | G | A | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.256+1023G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511303 | |||||||
| chr17:64511323 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.256+1043A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511323 | |||||||
| chr17:64511366 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01070.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.256+1086C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511366 | |||||||
| chr17:64511386 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0044 |
5 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.256+1106T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511386 | |||||||
| chr17:64511396 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.256+1116C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511396 | |||||||
| chr17:64511397 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.256+1117G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511397 | |||||||
| chr17:64511459 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.256+1179T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511459 | |||||||
| chr17:64511546 | C | A | 1 | a0001c0001t0002g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.256+1266C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511546 | |||||||
| chr17:64511663 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.256+1383C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511663 | |||||||
| chr17:64511802 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.256+1522C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511802 | |||||||
| chr17:64511884 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0053 |
3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.256+1604T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511884 | |||||||
| chr17:64511895 | G | A | 25 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
45 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.256+1615G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511895 | |||||||
| chr17:64511920 | T | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(7): Show |
14 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.256+1640T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64511920 | |||||||
| chr17:64512143 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.256+1863G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64512143 | |||||||
| chr17:64512251 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.256+1971C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64512251 | |||||||
| chr17:64513067 | T | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.257-1181T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513067 | |||||||
| chr17:64513527 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0004g0052 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.257-721A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513527 | |||||||
| chr17:64513842 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.257-406A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513842 | |||||||
| chr17:64513917 | A | G | 3 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0003g0012 |
4 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.257-331A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513917 | |||||||
| chr17:64513976 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.257-272G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64513976 | |||||||
| chr17:64514000 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.257-248C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514000 | |||||||
| chr17:64514034 | A | C | 1 | a0001c0001t0002g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.257-214A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514034 | |||||||
| chr17:64514064 | C | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(24): Show |
48 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.257-184C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514064 | |||||||
| chr17:64514078 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.257-170T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 3/19 | chr17 | 64514078 | |||||||
| chr17:64514379 | T | G | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.367+21T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514379 | |||||||
| chr17:64514882 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.367+524T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514882 | |||||||
| chr17:64514918 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.367+560C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64514918 | |||||||
| chr17:64514990 | C | CCTT | 39 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
62 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.367+633_367+634ins others(3): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr17 | 64514990 | ||||||
| chr17:64515299 | G | A | 1 | a0001c0001t0001g0010 | 4 | HG03017.hp2 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+941G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515299 | |||||||
| chr17:64515339 | A | C | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.367+981A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515339 | |||||||
| chr17:64515552 | C | G | 13 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
29 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.368-1171C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515552 | |||||||
| chr17:64515614 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368-1109A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515614 | |||||||
| chr17:64515955 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0120 others(5): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.368-768C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64515955 | |||||||
| chr17:64516122 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0053 |
3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.368-601T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516122 | |||||||
| chr17:64516127 | GT | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0121 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-595delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516127 | |||||||
| chr17:64516156 | A | T | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.368-567A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516156 | |||||||
| chr17:64516161 | C | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(7): Show |
26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-562C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516161 | |||||||
| chr17:64516344 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368-379G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516344 | |||||||
| chr17:64516493 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.368-230A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516493 | |||||||
| chr17:64516544 | C | A | 1 | a0004c0004t0002g0054 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.368-179C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 4/19 | chr17 | 64516544 | |||||||
| chr17:64517007 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.473+179C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517007 | |||||||
| chr17:64517015 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.473+187C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517015 | |||||||
| chr17:64517208 | G | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0048 |
5 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+380G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517208 | |||||||
| chr17:64517253 | G | A | 1 | a0001c0001t0002g0008 | 4 | HG01257.hp2 HG01258.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+425G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517253 | |||||||
| chr17:64517300 | T | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(139): Show |
245 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.473+472T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517300 | |||||||
| chr17:64517401 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.473+573A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517401 | |||||||
| chr17:64517407 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.473+579A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517407 | |||||||
| chr17:64517639 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0053 |
3 | HG02257.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.473+811G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517639 | |||||||
| chr17:64517672 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.473+844C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517672 | |||||||
| chr17:64517673 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+845G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517673 | |||||||
| chr17:64517690 | A | AT | 13 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(10): Show |
16 | HG00639.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.473+885dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr17 | 64517690 | ||||||
| chr17:64517690 | AT | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0070 a0001c0001t0001g0071 others(3): Show |
8 | HG01257.hp1 HG02129.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+885delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr17 | 64517690 | ||||||
| chr17:64517772 | G | A | 1 | a0007c0007t0002g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+944G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64517772 | |||||||
| chr17:64518028 | C | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(7): Show |
26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.473+1200C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518028 | |||||||
| chr17:64518400 | G | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0003g0012 |
4 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-921G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518400 | |||||||
| chr17:64518403 | T | C | 1 | a0001c0001t0001g0022 | 2 | NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.474-918T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518403 | |||||||
| chr17:64518617 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-704A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518617 | |||||||
| chr17:64518637 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.474-684A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518637 | |||||||
| chr17:64518826 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-495G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518826 | |||||||
| chr17:64518838 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.474-483G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518838 | |||||||
| chr17:64518899 | C | T | 1 | a0007c0007t0002g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-422C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518899 | |||||||
| chr17:64518920 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474-401A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518920 | |||||||
| chr17:64518961 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.474-360G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518961 | |||||||
| chr17:64518976 | C | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.474-345C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64518976 | |||||||
| chr17:64519077 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.474-244C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519077 | |||||||
| chr17:64519091 | C | G | 3 | a0001c0001t0002g0132 a0002c0002t0002g0130 a0002c0002t0002g0131 |
3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.474-230C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519091 | |||||||
| chr17:64519218 | G | A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.474-103G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 5/19 | chr17 | 64519218 | |||||||
| chr17:64519535 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.589+99C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519535 | |||||||
| chr17:64519605 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.589+169C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519605 | |||||||
| chr17:64519817 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.589+381T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519817 | |||||||
| chr17:64519866 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.589+430A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64519866 | |||||||
| chr17:64520123 | T | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.589+687T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520123 | |||||||
| chr17:64520183 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.589+747C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520183 | |||||||
| chr17:64520248 | CATT | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.589+815_589+817del others(3): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr17 | 64520248 | ||||||
| chr17:64520458 | CT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(124): Show |
226 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.590-925delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr17 | 64520458 | ||||||
| chr17:64520520 | C | T | 1 | a0010c0006t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.590-882C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520520 | |||||||
| chr17:64520747 | A | G | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.590-655A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520747 | |||||||
| chr17:64520786 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.590-616A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520786 | |||||||
| chr17:64520841 | A | C | 1 | a0001c0001t0002g0100 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.590-561A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64520841 | |||||||
| chr17:64521059 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.590-343A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521059 | |||||||
| chr17:64521193 | C | T | 1 | a0001c0001t0002g0033 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.590-209C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521193 | |||||||
| chr17:64521217 | CAA | C | 9 | a0001c0001t0001g0110 a0001c0001t0002g0013 a0001c0001t0002g0017 others(6): Show |
13 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.590-184_590-183del others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521217 | |||||||
| chr17:64521232 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.590-170G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521232 | |||||||
| chr17:64521346 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.590-56G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521346 | |||||||
| chr17:64521358 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.590-44A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 6/19 | chr17 | 64521358 | |||||||
| chr17:64521580 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0098 |
3 | NA19009.hp1 NA19011.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.715+53A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521580 | |||||||
| chr17:64521867 | A | G | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.715+340A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521867 | |||||||
| chr17:64521874 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0064 |
5 | NA18956.hp1 NA18970.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+347C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521874 | |||||||
| chr17:64521970 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715+443C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64521970 | |||||||
| chr17:64522259 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.716-443T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522259 | |||||||
| chr17:64522259 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-443T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522259 | |||||||
| chr17:64522263 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-439A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522263 | |||||||
| chr17:64522265 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-437A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522265 | |||||||
| chr17:64522269 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-433T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522269 | |||||||
| chr17:64522271 | A | G | 4 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
4 | HG02818.hp2 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-431A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522271 | |||||||
| chr17:64522276 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-426C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522276 | |||||||
| chr17:64522276 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.716-426C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522276 | |||||||
| chr17:64522283 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-419C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522283 | |||||||
| chr17:64522286 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-416T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522286 | |||||||
| chr17:64522288 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-414T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522288 | |||||||
| chr17:64522290 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-412A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522290 | |||||||
| chr17:64522291 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-411G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522291 | |||||||
| chr17:64522294 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-408G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522294 | |||||||
| chr17:64522301 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-401G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522301 | |||||||
| chr17:64522302 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-400T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522302 | |||||||
| chr17:64522304 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-398T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522304 | |||||||
| chr17:64522308 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-394A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522308 | |||||||
| chr17:64522310 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-392G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522310 | |||||||
| chr17:64522311 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-391T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522311 | |||||||
| chr17:64522314 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-388C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522314 | |||||||
| chr17:64522315 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-387T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522315 | |||||||
| chr17:64522341 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-361A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522341 | |||||||
| chr17:64522342 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-360C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522342 | |||||||
| chr17:64522344 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-358T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522344 | |||||||
| chr17:64522345 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-357T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522345 | |||||||
| chr17:64522347 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-355A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522347 | |||||||
| chr17:64522351 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-351T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522351 | |||||||
| chr17:64522353 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-349C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522353 | |||||||
| chr17:64522354 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-348A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522354 | |||||||
| chr17:64522356 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-346C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522356 | |||||||
| chr17:64522358 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-344G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522358 | |||||||
| chr17:64522359 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-343G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522359 | |||||||
| chr17:64522364 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-338A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522364 | |||||||
| chr17:64522366 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-336T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522366 | |||||||
| chr17:64522369 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-333T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522369 | |||||||
| chr17:64522380 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-322A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522380 | |||||||
| chr17:64522390 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-312C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522390 | |||||||
| chr17:64522425 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-277T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522425 | |||||||
| chr17:64522426 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-276G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522426 | |||||||
| chr17:64522427 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-275A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522427 | |||||||
| chr17:64522429 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-273C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522429 | |||||||
| chr17:64522432 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-270A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522432 | |||||||
| chr17:64522433 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-269G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522433 | |||||||
| chr17:64522453 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-249G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522453 | |||||||
| chr17:64522462 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-240C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522462 | |||||||
| chr17:64522463 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-239G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522463 | |||||||
| chr17:64522464 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-238A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522464 | |||||||
| chr17:64522467 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-235C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522467 | |||||||
| chr17:64522469 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.716-233T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522469 | |||||||
| chr17:64522493 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0047 |
2 | HG02015.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.716-209A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522493 | |||||||
| chr17:64522504 | A | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(3): Show |
10 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.716-198A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522504 | |||||||
| chr17:64522694 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(4): Show |
11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.716-8C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 7/19 | chr17 | 64522694 | |||||||
| chr17:64522979 | CGTGTGT | C | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.909+89_909+94delGT others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64522979 | ||||||
| chr17:64523152 | C | T | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.909+257C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523152 | |||||||
| chr17:64523319 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.909+424A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523319 | |||||||
| chr17:64523337 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.909+442A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523337 | |||||||
| chr17:64523389 | G | A | 8 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0120 others(5): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+494G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523389 | |||||||
| chr17:64523566 | C | CA | 3 | a0001c0001t0001g0023 a0001c0001t0002g0016 a0001c0001t0002g0053 |
5 | HG02257.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+683dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | ||||||
| chr17:64523566 | C | CAA | 10 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(7): Show |
21 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.909+682_909+683dup others(2): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | ||||||
| chr17:64523566 | CA | C | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+683delA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64523566 | ||||||
| chr17:64523682 | T | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(44): Show |
79 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.909+787T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523682 | |||||||
| chr17:64523793 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909+898A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523793 | |||||||
| chr17:64523910 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.909+1015A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523910 | |||||||
| chr17:64523965 | A | G | 15 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(12): Show |
31 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.909+1070A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523965 | |||||||
| chr17:64523968 | T | C | 65 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(62): Show |
110 | HG00558.hp2 HG00639.hp1 HG01069.hp2 others(107): Show |
intron_variant | MODIFIER | c.909+1073T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64523968 | |||||||
| chr17:64524005 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.909+1110C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524005 | |||||||
| chr17:64524151 | T | G | 2 | a0001c0001t0001g0076 a0003c0008t0001g0077 |
2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.909+1256T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524151 | |||||||
| chr17:64524170 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.909+1275G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524170 | |||||||
| chr17:64524307 | T | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG01175.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.909+1412T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524307 | |||||||
| chr17:64524477 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.910-1293T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524477 | |||||||
| chr17:64524483 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.910-1287T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524483 | |||||||
| chr17:64524514 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.910-1256C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524514 | |||||||
| chr17:64524551 | C | T | 34 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(31): Show |
55 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.910-1219C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524551 | |||||||
| chr17:64524609 | C | A | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.910-1161C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524609 | |||||||
| chr17:64524823 | T | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.910-947T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524823 | |||||||
| chr17:64524833 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.910-937C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64524833 | |||||||
| chr17:64524968 | C | CA | 8 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(5): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-796dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr17 | 64524968 | ||||||
| chr17:64525031 | A | G | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.910-739A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525031 | |||||||
| chr17:64525063 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.910-707G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525063 | |||||||
| chr17:64525317 | C | G | 1 | a0001c0001t0001g0022 | 2 | NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.910-453C>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525317 | |||||||
| chr17:64525373 | G | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(7): Show |
26 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-397G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525373 | |||||||
| chr17:64525382 | T | C | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(7): Show |
12 | HG01346.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-388T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525382 | |||||||
| chr17:64525513 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.910-257T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525513 | |||||||
| chr17:64525645 | A | G | 2 | a0001c0001t0001g0076 a0003c0008t0001g0077 |
2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.910-125A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525645 | |||||||
| chr17:64525656 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0096 |
3 | HG00673.hp2 NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.910-114C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 8/19 | chr17 | 64525656 | |||||||
| chr17:64525908 | T | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0040 others(6): Show |
19 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022+26T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 9/19 | chr17 | 64525908 | |||||||
| chr17:64525937 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(6): Show |
11 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022+55A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 9/19 | chr17 | 64525937 | |||||||
| chr17:64526237 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1152+37T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526237 | |||||||
| chr17:64526712 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1153-399A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526712 | |||||||
| chr17:64526764 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1153-347C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526764 | |||||||
| chr17:64526939 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-172G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 10/19 | chr17 | 64526939 | |||||||
| chr17:64527850 | TAA | T | 3 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02818.hp2 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1306+587_1306+588d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527850 | |||||||
| chr17:64527850 | TAATG | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0120 others(1): Show |
14 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306+587_1306+590d others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527850 | |||||||
| chr17:64527851 | A | T | 1 | a0001c0001t0002g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1306+587A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527851 | |||||||
| chr17:64527852 | A | ATG | 4 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0108 others(1): Show |
5 | HG00597.hp2 HG00642.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+606_1306+607d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | ||||||
| chr17:64527852 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1306+588A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527852 | |||||||
| chr17:64527852 | ATG | A | 5 | a0001c0001t0002g0016 a0001c0001t0002g0018 a0001c0001t0002g0053 others(2): Show |
6 | HG02257.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+606_1306+607d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | ||||||
| chr17:64527852 | ATGTG | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(7): Show |
13 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306+604_1306+607d others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527852 | ||||||
| chr17:64527860 | G | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1306+596G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527860 | |||||||
| chr17:64527866 | G | GTA | 6 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0135 others(3): Show |
7 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306+603_1306+604i others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | ||||||
| chr17:64527866 | G | GTATA | 5 | a0001c0001t0002g0032 a0001c0001t0002g0139 a0001c0001t0002g0140 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+603_1306+604i others(6): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | ||||||
| chr17:64527866 | GTGTGTA | G | 15 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(12): Show |
32 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306+604_1306+609d others(8): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527866 | ||||||
| chr17:64527868 | G | A | 16 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(13): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306+604G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527868 | |||||||
| chr17:64527870 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0002g0016 others(25): Show |
31 | HG00323.hp1 HG00639.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1306+606G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527870 | |||||||
| chr17:64527870 | G | GTA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0074 a0001c0001t0001g0097 others(8): Show |
19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306+627_1306+628d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527870 | ||||||
| chr17:64527872 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1306+608A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527872 | |||||||
| chr17:64527889 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0062 others(1): Show |
6 | NA18956.hp1 NA18970.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+625T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527889 | |||||||
| chr17:64527891 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0019 others(12): Show |
21 | HG00597.hp2 HG00642.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1306+627T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527891 | |||||||
| chr17:64527891 | T | TAC | 25 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0022 others(22): Show |
39 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1306+642_1306+643d others(4): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr17 | 64527891 | ||||||
| chr17:64527893 | C | T | 26 | a0001c0001t0001g0095 a0001c0001t0002g0002 a0001c0001t0002g0007 others(23): Show |
45 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1306+629C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527893 | |||||||
| chr17:64527904 | A | G | 3 | a0001c0001t0002g0132 a0002c0002t0002g0130 a0002c0002t0002g0131 |
3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1306+640A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527904 | |||||||
| chr17:64527910 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0125 |
2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1306+646G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64527910 | |||||||
| chr17:64528354 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1307-934T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528354 | |||||||
| chr17:64528359 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
7 | NA18942.hp2 NA18956.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-929T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528359 | |||||||
| chr17:64528478 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1307-810A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528478 | |||||||
| chr17:64528628 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00639.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1307-660C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528628 | |||||||
| chr17:64528963 | G | A | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1307-325G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64528963 | |||||||
| chr17:64529025 | A | G | 1 | a0007c0007t0002g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1307-263A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529025 | |||||||
| chr17:64529060 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1307-228G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529060 | |||||||
| chr17:64529099 | C | T | 1 | a0005c0005t0002g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1307-189C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 11/19 | chr17 | 64529099 | |||||||
| chr17:64529454 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1446+27T>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529454 | |||||||
| chr17:64529586 | T | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(45): Show |
81 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.1446+159T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529586 | |||||||
| chr17:64529714 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG02280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1446+287T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64529714 | |||||||
| chr17:64530064 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1446+637A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530064 | |||||||
| chr17:64530122 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1446+695A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530122 | |||||||
| chr17:64530176 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1446+749G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530176 | |||||||
| chr17:64530178 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1447-748G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530178 | |||||||
| chr17:64530250 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1447-676G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530250 | |||||||
| chr17:64530342 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1447-584T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530342 | |||||||
| chr17:64530482 | A | G | 35 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(32): Show |
57 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1447-444A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530482 | |||||||
| chr17:64530546 | C | T | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1447-380C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530546 | |||||||
| chr17:64530564 | A | G | 8 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0120 others(5): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447-362A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530564 | |||||||
| chr17:64530756 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1447-170T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530756 | |||||||
| chr17:64530869 | G | T | 1 | a0001c0001t0002g0016 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1447-57G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 12/19 | chr17 | 64530869 | |||||||
| chr17:64531253 | TC | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0120 others(5): Show |
18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1539+238delC | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr17 | 64531253 | ||||||
| chr17:64531526 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1540-364A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531526 | |||||||
| chr17:64531587 | G | A | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(44): Show |
80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1540-303G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531587 | |||||||
| chr17:64531699 | G | A | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(44): Show |
80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1540-191G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531699 | |||||||
| chr17:64531705 | T | A | 1 | a0001c0001t0001g0010 | 4 | HG03017.hp2 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-185T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531705 | |||||||
| chr17:64531757 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1540-133G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 13/19 | chr17 | 64531757 | |||||||
| chr17:64532061 | A | G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(44): Show |
80 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.1672+39A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532061 | |||||||
| chr17:64532125 | C | CGAAGAAA others(4): Show |
1 | a0001c0001t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1672+104_1672+114d others(13): Show |
CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532125 | ||||||
| chr17:64532133 | G | GT | 9 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(6): Show |
19 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1672+123dupT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532133 | ||||||
| chr17:64532133 | GT | G | 9 | a0001c0001t0001g0064 a0001c0001t0002g0004 a0001c0001t0002g0015 others(6): Show |
19 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1672+123delT | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr17 | 64532133 | ||||||
| chr17:64532169 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1672+147T>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532169 | |||||||
| chr17:64532181 | G | A | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1672+159G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532181 | |||||||
| chr17:64532204 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1672+182G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532204 | |||||||
| chr17:64532268 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1672+246C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532268 | |||||||
| chr17:64532282 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0096 |
3 | HG00673.hp2 NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1672+260G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532282 | |||||||
| chr17:64532287 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1672+265C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532287 | |||||||
| chr17:64532523 | C | T | 3 | a0001c0001t0002g0132 a0002c0002t0002g0130 a0002c0002t0002g0131 |
3 | HG02109.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1673-316C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532523 | |||||||
| chr17:64532528 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1673-311G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532528 | |||||||
| chr17:64532547 | G | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1673-292G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532547 | |||||||
| chr17:64532708 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(11): Show |
30 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1673-131A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 14/19 | chr17 | 64532708 | |||||||
| chr17:64533110 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1843-7C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 15/19 | chr17 | 64533110 | |||||||
| chr17:64533244 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1917+53C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533244 | |||||||
| chr17:64533298 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1917+107C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533298 | |||||||
| chr17:64533452 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1917+261A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533452 | |||||||
| chr17:64533880 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1917+689C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533880 | |||||||
| chr17:64533958 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1918-627C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64533958 | |||||||
| chr17:64534018 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1918-567C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534018 | |||||||
| chr17:64534025 | G | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0040 others(3): Show |
15 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1918-560G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534025 | |||||||
| chr17:64534163 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1918-422G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534163 | |||||||
| chr17:64534175 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1918-410T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 16/19 | chr17 | 64534175 | |||||||
| chr17:64534788 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0116 |
3 | HG00323.hp1 HG01070.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2070+51C>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64534788 | |||||||
| chr17:64535296 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2070+559T>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535296 | |||||||
| chr17:64535580 | C | T | 8 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(5): Show |
12 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070+843C>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535580 | |||||||
| chr17:64535582 | A | C | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(7): Show |
12 | HG01346.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070+845A>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535582 | |||||||
| chr17:64535694 | A | G | 1 | a0001c0001t0002g0031 | 2 | HG01346.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2071-908A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535694 | |||||||
| chr17:64535954 | A | G | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2071-648A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64535954 | |||||||
| chr17:64536201 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2071-401G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536201 | |||||||
| chr17:64536260 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2071-342G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536260 | |||||||
| chr17:64536270 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2071-332G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536270 | |||||||
| chr17:64536484 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2071-118A>G | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536484 | |||||||
| chr17:64536494 | A | T | 1 | a0006c0003t0002g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2071-108A>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536494 | |||||||
| chr17:64536504 | T | TA | 8 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(5): Show |
12 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.2071-86dupA | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr17 | 64536504 | ||||||
| chr17:64536521 | G | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0018 others(4): Show |
11 | HG02109.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.2071-81G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536521 | |||||||
| chr17:64536522 | G | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(24): Show |
48 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.2071-80G>T | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 17/19 | chr17 | 64536522 | |||||||
| chr17:64536888 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2217+140G>C | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 18/19 | chr17 | 64536888 | |||||||
| chr17:64537510 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2290-93G>A | CEP95 | ENSG00000258890.8 | transcript | ENST00000556440.7 | protein_coding | 19/19 | chr17 | 64537510 |