Item | Value |
---|---|
geneid | 22995 |
ensemblid | ENSG00000103995.14 |
hgncid | 29298 |
symbol | CEP152 |
name | centrosomal protein 152 |
refseq_nuc | NM_001194998.2 |
refseq_prot | NP_001181927.1 |
ensembl_nuc | ENST00000380950.7 |
ensembl_prot | ENSP00000370337.2 |
mane_status | MANE Select |
chr | chr15 |
start | 48737938 |
end | 48811069 |
strand | - |
ver | v1.2 |
region | chr15:48737938-48811069 |
region5000 | chr15:48732938-48816069 |
regionname0 | CEP152_chr15_48737938_48811069 |
regionname5000 | CEP152_chr15_48732938_48816069 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1710 | 220 | 59 | 36 | 81 | 14 | 28 | 64 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0002 | 0/0 | 1710 | 44 | 0 | 5 | 32 | 0 | 7 | 24 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0003 | 0/0 | 1710 | 27 | 0 | 4 | 23 | 0 | 0 | 19 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0004 | 0/0 | 1710 | 16 | 1 | 1 | 14 | 0 | 0 | 9 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0005 | 0/0 | 1710 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0006 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0007 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0008 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0009 | 0/0 | 1710 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0010 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0011 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0012 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0013 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0014 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0015 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0016 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0017 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0018 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0019 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1357): Show |
chr15 | 48732938 | 48816069 |
a0020 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0021 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0022 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0023 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0024 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0025 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0026 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0027 | 0/0 | 1710 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0028 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
a0029 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | MSLDF others(1705): Show |
chr15 | 48732938 | 48816069 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5130 | 211 | 55 | 36 | 77 | 13 | 28 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0007 | 0/0 | 5130 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0009 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0014 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0016 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0023 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0024 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0001c0036 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0002c0002 | 0/0 | 5130 | 42 | 0 | 5 | 31 | 0 | 6 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0002c0037 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0002c0038 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0003c0003 | 0/0 | 5130 | 27 | 0 | 4 | 23 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0004c0004 | 0/0 | 5130 | 16 | 1 | 1 | 14 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0005c0005 | 0/0 | 5130 | 4 | 4 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0006c0006 | 0/0 | 5130 | 3 | 3 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0007c0012 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0007c0017 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0008c0011 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0009c0008 | 0/0 | 5130 | 2 | 0 | 0 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0010c0010 | 0/0 | 5130 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0011c0015 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0012c0013 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0013c0033 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0014c0018 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0015c0031 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0016c0029 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0017c0039 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0018c0027 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0019c0025 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0020c0021 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0021c0026 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0022c0034 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0023c0035 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0024c0022 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0025c0020 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0026c0032 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0027c0019 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0028c0028 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 | ||
a0029c0030 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | ATGTC others(5125): Show |
chr15 | 48732938 | 48816069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5560 | 158 | 45 | 25 | 56 | 12 | 18 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0001t0002 | 0/0 | 5560 | 40 | 8 | 5 | 21 | 1 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0001t0003 | 0/0 | 5560 | 9 | 0 | 4 | 0 | 0 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0001t0004 | 0/0 | 5560 | 4 | 2 | 2 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0007t0001 | 0/0 | 5560 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0009t0005 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0014t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0016t0004 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0023t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0024t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0001c0036t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0002c0002t0002 | 0/0 | 5560 | 41 | 0 | 5 | 31 | 0 | 5 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0002c0002t0006 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0002c0037t0007 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0002c0038t0002 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0003c0003t0001 | 0/0 | 5560 | 24 | 0 | 4 | 20 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0003c0003t0002 | 0/0 | 5560 | 3 | 0 | 0 | 3 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0004c0004t0001 | 0/0 | 5560 | 16 | 1 | 1 | 14 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0005c0005t0001 | 0/0 | 5560 | 4 | 4 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0006c0006t0001 | 0/0 | 5560 | 3 | 3 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0007c0012t0001 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0007c0017t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0008c0011t0001 | 0/0 | 5560 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0009c0008t0001 | 0/0 | 5560 | 2 | 0 | 0 | 0 | 0 | 2 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0010c0010t0001 | 0/0 | 5560 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0011c0015t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0012c0013t0001 | 0/0 | 5560 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0013c0033t0001 | 0/0 | 5560 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0014c0018t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0015c0031t0002 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0016c0029t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0017c0039t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0018c0027t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0019c0025t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0020c0021t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0021c0026t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0022c0034t0001 | 0/0 | 5560 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0023c0035t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0024c0022t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0025c0020t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0026c0032t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0027c0019t0001 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0028c0028t0002 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
a0029c0030t0001 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | GTGAC others(5555): Show |
chr15 | 48732938 | 48816069 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0007t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0007t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0009t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0009t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0014t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0016t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0023t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0024t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0001c0036t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0037t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0002c0038t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0003c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0004c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0005c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0006c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0012t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0012t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0007c0017t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0008c0011t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0008c0011t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0009c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0009c0008t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0010c0010t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0011c0015t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0012c0013t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0013c0033t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0014c0018t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0015c0031t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0016c0029t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0017c0039t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0018c0027t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0019c0025t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0020c0021t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0021c0026t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0022c0034t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0023c0035t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0024c0022t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0025c0020t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0026c0032t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0027c0019t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0028c0028t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
a0029c0030t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00099 | hp2 | a0001 | c0016 | t0004 | g0108 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0317 | EUR | GBR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00597 | hp2 | a0011 | c0015 | t0001 | g0140 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00735 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0248 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01081 | hp2 | a0012 | c0013 | t0001 | g0079 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01106 | hp1 | a0013 | c0033 | t0001 | g0111 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | PUR | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01255 | hp2 | a0004 | c0004 | t0001 | g0143 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0265 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01884 | hp1 | a0014 | c0018 | t0001 | g0232 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01884 | hp2 | a0006 | c0006 | t0001 | g0020 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01891 | hp1 | a0015 | c0031 | t0002 | g0321 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0155 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0157 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02027 | hp2 | a0016 | c0029 | t0001 | g0154 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0050 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0141 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02056 | hp2 | a0004 | c0004 | t0001 | g0038 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02074 | hp2 | a0017 | c0039 | t0002 | g0256 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02129 | hp1 | a0018 | c0027 | t0001 | g0179 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02132 | hp2 | a0004 | c0004 | t0001 | g0142 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | CDX | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02257 | hp2 | a0007 | c0012 | t0001 | g0062 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02258 | hp1 | a0001 | c0024 | t0001 | g0136 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02451 | hp1 | a0019 | c0025 | t0001 | g0231 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02622 | hp1 | a0020 | c0021 | t0001 | g0135 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02630 | hp1 | a0001 | c0009 | t0005 | g0022 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02630 | hp2 | a0005 | c0005 | t0001 | g0043 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0054 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02717 | hp2 | a0008 | c0011 | t0001 | g0094 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03017 | hp1 | a0002 | c0038 | t0002 | g0267 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03041 | hp1 | a0007 | c0012 | t0001 | g0075 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03041 | hp2 | a0021 | c0026 | t0001 | g0132 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03130 | hp2 | a0005 | c0005 | t0001 | g0051 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03209 | hp1 | a0006 | c0006 | t0001 | g0025 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03225 | hp1 | a0005 | c0005 | t0001 | g0052 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03225 | hp2 | a0007 | c0017 | t0001 | g0026 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03453 | hp1 | a0006 | c0006 | t0001 | g0021 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03491 | hp1 | a0002 | c0002 | t0006 | g0266 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03491 | hp2 | a0022 | c0034 | t0001 | g0126 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03516 | hp1 | a0008 | c0011 | t0001 | g0095 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03540 | hp1 | a0001 | c0009 | t0005 | g0023 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03831 | hp1 | a0009 | c0008 | t0001 | g0187 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0269 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04184 | hp1 | a0009 | c0008 | t0001 | g0122 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0250 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0258 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | STU | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18612 | hp1 | a0004 | c0004 | t0001 | g0168 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0049 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0296 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18943 | hp1 | a0023 | c0035 | t0001 | g0071 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18949 | hp1 | a0004 | c0004 | t0001 | g0139 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18956 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0093 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18965 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0208 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18975 | hp1 | a0001 | c0007 | t0001 | g0214 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18981 | hp1 | a0010 | c0010 | t0001 | g0006 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18985 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18988 | hp1 | a0002 | c0037 | t0007 | g0327 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18992 | hp1 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18993 | hp1 | a0025 | c0020 | t0001 | g0069 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18993 | hp2 | a0004 | c0004 | t0001 | g0146 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19000 | hp1 | a0026 | c0032 | t0001 | g0148 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19002 | hp1 | a0003 | c0003 | t0002 | g0310 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19030 | hp1 | a0027 | c0019 | t0001 | g0109 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19059 | hp2 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19060 | hp2 | a0028 | c0028 | t0002 | g0286 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19076 | hp2 | a0001 | c0007 | t0001 | g0181 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19079 | hp1 | a0001 | c0014 | t0001 | g0178 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0008 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19084 | hp1 | a0010 | c0010 | t0001 | g0006 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19087 | hp1 | a0029 | c0030 | t0001 | g0207 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19087 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19089 | hp1 | a0001 | c0036 | t0002 | g0311 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19089 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ASW | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ASW | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
HG06807 | hp2 | a0001 | c0023 | t0001 | g0115 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA18955 | hp2 | a0024 | c0022 | t0001 | g0045 | EAS | JPT | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0204 | REF | REF | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0120 | REF | REF | CEP152_chr15_48732938_48816069 | CEP152 | chr15 | 48732938 | 48816069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738304 | G | A | 1 | a0009 | 2 | HG03831.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.5078C>T | p.Pro1693Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5194/5560 | 5078/5133 | 1693/1710 | chr15 | 48738304 | |||
chr15:48738625 | C | G | 1 | a0016 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.4757G>C | p.Arg1586Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4873/5560 | 4757/5133 | 1586/1710 | chr15 | 48738625 | |||
chr15:48739207 | A | G | 1 | a0024 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.4175T>C | p.Ile1392Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4291/5560 | 4175/5133 | 1392/1710 | chr15 | 48739207 | |||
chr15:48741607 | G | A | 1 | a0019 | 1 | HG02451.hp1 | stop_gained | HIGH | c.4087C>T | p.Gln1363* | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/27 | 4203/5560 | 4087/5133 | 1363/1710 | chr15 | 48741607 | |||
chr15:48741617 | G | C | 1 | a0021 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.4077C>G | p.Ser1359Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/27 | 4193/5560 | 4077/5133 | 1359/1710 | chr15 | 48741617 | |||
chr15:48742014 | C | T | 1 | a0020 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3922G>A | p.Ala1308Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 25/27 | 4038/5560 | 3922/5133 | 1308/1710 | chr15 | 48742014 | |||
chr15:48744900 | G | C | 1 | a0029 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.3727C>G | p.Pro1243Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/27 | 3843/5560 | 3727/5133 | 1243/1710 | chr15 | 48744900 | |||
chr15:48744915 | G | C | 1 | a0021 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3712C>G | p.Leu1238Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/27 | 3828/5560 | 3712/5133 | 1238/1710 | chr15 | 48744915 | |||
chr15:48748540 | C | G | 1 | a0005 | 4 | HG02630.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.3537G>C | p.Lys1179Asn | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/27 | 3653/5560 | 3537/5133 | 1179/1710 | chr15 | 48748540 | |||
chr15:48752382 | G | T | 1 | a0025 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.3433C>A | p.Pro1145Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3549/5560 | 3433/5133 | 1145/1710 | chr15 | 48752382 | |||
chr15:48752460 | C | T | 1 | a0027 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3355G>A | p.Ala1119Thr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3471/5560 | 3355/5133 | 1119/1710 | chr15 | 48752460 | |||
chr15:48755923 | C | G | 1 | a0014 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3325G>C | p.Ala1109Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3441/5560 | 3325/5133 | 1109/1710 | chr15 | 48755923 | |||
chr15:48755931 | A | G | 2 | a0007 a0008 |
5 | HG02257.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3317T>C | p.Val1106Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3433/5560 | 3317/5133 | 1106/1710 | chr15 | 48755931 | |||
chr15:48755970 | C | T | 1 | a0006 | 3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.3278G>A | p.Cys1093Tyr | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 3394/5560 | 3278/5133 | 1093/1710 | chr15 | 48755970 | |||
chr15:48756379 | G | A | 1 | a0029 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.2869C>T | p.Arg957Trp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2985/5560 | 2869/5133 | 957/1710 | chr15 | 48756379 | |||
chr15:48756444 | T | C | 1 | a0018 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.2804A>G | p.Gln935Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2920/5560 | 2804/5133 | 935/1710 | chr15 | 48756444 | |||
chr15:48756471 | T | A | 1 | a0010 | 2 | NA18981.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.2777A>T | p.Glu926Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2893/5560 | 2777/5133 | 926/1710 | chr15 | 48756471 | |||
chr15:48756508 | G | C | 1 | a0004 | 16 | HG00558.hp2 HG01255.hp2 HG02040.hp2 others(13): Show |
missense_variant | MODERATE | c.2740C>G | p.Leu914Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/27 | 2856/5560 | 2740/5133 | 914/1710 | chr15 | 48756508 | |||
chr15:48760148 | G | A | 2 | a0026 a0028 |
2 | NA19000.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.2681C>T | p.Ser894Phe | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/27 | 2797/5560 | 2681/5133 | 894/1710 | chr15 | 48760148 | |||
chr15:48762575 | C | A | 4 | a0003 a0016 a0017 others(1): Show |
30 | HG00735.hp2 HG01981.hp2 HG02004.hp1 others(27): Show |
missense_variant | MODERATE | c.2378G>T | p.Ser793Ile | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/27 | 2494/5560 | 2378/5133 | 793/1710 | chr15 | 48762575 | |||
chr15:48762612 | T | C | 2 | a0015 a0026 |
2 | HG01891.hp1 NA19000.hp1 |
missense_variant | MODERATE | c.2341A>G | p.Ile781Val | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/27 | 2457/5560 | 2341/5133 | 781/1710 | chr15 | 48762612 | |||
chr15:48767136 | T | C | 1 | a0013 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.2204A>G | p.Glu735Gly | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/27 | 2320/5560 | 2204/5133 | 735/1710 | chr15 | 48767136 | |||
chr15:48768237 | T | C | 1 | a0008 | 2 | HG02717.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2000A>G | p.Lys667Arg | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/27 | 2116/5560 | 2000/5133 | 667/1710 | chr15 | 48768237 | |||
chr15:48784063 | C | G | 1 | a0011 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1231G>C | p.Ala411Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/27 | 1347/5560 | 1231/5133 | 411/1710 | chr15 | 48784063 | |||
chr15:48788836 | T | C | 1 | a0022 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1138A>G | p.Asn380Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/27 | 1254/5560 | 1138/5133 | 380/1710 | chr15 | 48788836 | |||
chr15:48793394 | C | A | 1 | a0023 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.759G>T | p.Glu253Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/27 | 875/5560 | 759/5133 | 253/1710 | chr15 | 48793394 | |||
chr15:48797497 | C | T | 1 | a0012 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.344G>A | p.Arg115Gln | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/27 | 460/5560 | 344/5133 | 115/1710 | chr15 | 48797497 | |||
chr15:48797978 | G | A | 2 | a0002 a0017 |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
missense_variant | MODERATE | c.161C>T | p.Ser54Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/27 | 277/5560 | 161/5133 | 54/1710 | chr15 | 48797978 | |||
chr15:48810963 | G | C | 1 | a0002 | 1 | NA18988.hp1 | splice_region_variant | LOW | c.-10C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | chr15 | 48810963 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738267 | T | C | 1 | a0001c0024 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.5115A>G | p.Pro1705Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5231/5560 | 5115/5133 | 1705/1710 | chr15 | 48738267 | |||
chr15:48738303 | C | T | 1 | a0002c0038 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.5079G>A | p.Pro1693Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5195/5560 | 5079/5133 | 1693/1710 | chr15 | 48738303 | |||
chr15:48738468 | T | C | 1 | a0001c0009 | 2 | HG02630.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.4914A>G | p.Pro1638Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5030/5560 | 4914/5133 | 1638/1710 | chr15 | 48738468 | |||
chr15:48738510 | A | G | 1 | a0002c0037 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.4872T>C | p.Asn1624Asn | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4988/5560 | 4872/5133 | 1624/1710 | chr15 | 48738510 | |||
chr15:48738525 | A | G | 2 | a0001c0024 a0014c0018 |
2 | HG01884.hp1 HG02258.hp1 |
synonymous_variant | LOW | c.4857T>C | p.Asp1619Asp | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4973/5560 | 4857/5133 | 1619/1710 | chr15 | 48738525 | |||
chr15:48738909 | C | G | 1 | a0001c0023 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4473G>C | p.Pro1491Pro | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4589/5560 | 4473/5133 | 1491/1710 | chr15 | 48738909 | |||
chr15:48739083 | A | G | 1 | a0008c0011 | 2 | HG02717.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.4299T>C | p.His1433His | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 4415/5560 | 4299/5133 | 1433/1710 | chr15 | 48739083 | |||
chr15:48752386 | A | C | 1 | a0001c0007 | 2 | NA18975.hp1 NA19076.hp2 |
synonymous_variant | LOW | c.3429T>G | p.Ala1143Ala | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/27 | 3545/5560 | 3429/5133 | 1143/1710 | chr15 | 48752386 | |||
chr15:48767078 | C | T | 1 | a0001c0016 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2262G>A | p.Glu754Glu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/27 | 2378/5560 | 2262/5133 | 754/1710 | chr15 | 48767078 | |||
chr15:48768998 | C | A | 1 | a0007c0012 | 2 | HG02257.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.1866G>T | p.Leu622Leu | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/27 | 1982/5560 | 1866/5133 | 622/1710 | chr15 | 48768998 | |||
chr15:48796104 | C | T | 1 | a0001c0014 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.597G>A | p.Gln199Gln | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/27 | 713/5560 | 597/5133 | 199/1710 | chr15 | 48796104 | |||
chr15:48797541 | T | C | 1 | a0001c0036 | 1 | NA19089.hp1 | synonymous_variant | LOW | c.300A>G | p.Lys100Lys | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/27 | 416/5560 | 300/5133 | 100/1710 | chr15 | 48797541 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48738055 | C | T | 1 | a0001c0009t0005 | 2 | HG02630.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*194G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 194 | chr15 | 48738055 | ||||||
chr15:48738079 | A | G | 2 | a0001c0001t0004 a0001c0016t0004 |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 170 | chr15 | 48738079 | ||||||
chr15:48738244 | C | A | 1 | a0002c0002t0006 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 27/27 | 5 | chr15 | 48738244 | ||||||
chr15:48810977 | T | A | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | chr15 | 48810977 | |||||||
chr15:48810978 | G | T | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5329 | chr15 | 48810978 | ||||||
chr15:48810979 | T | A | 1 | a0001c0001t0003 | 9 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-26A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5330 | chr15 | 48810979 | ||||||
chr15:48811047 | T | C | 10 | a0001c0001t0002 a0001c0036t0002 a0002c0002t0002 others(7): Show |
91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-94A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/27 | 5398 | chr15 | 48811047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:48739297 | T | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4094-9A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739297 | |||||||
chr15:48739342 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4094-54C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739342 | |||||||
chr15:48739364 | TA | T | 5 | a0007c0012t0001g0062 a0007c0012t0001g0075 a0007c0017t0001g0026 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-77delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739364 | |||||||
chr15:48739811 | A | G | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4094-523T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739811 | |||||||
chr15:48739940 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4094-652G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48739940 | |||||||
chr15:48740168 | C | G | 1 | a0002c0002t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4094-880G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740168 | |||||||
chr15:48740211 | T | C | 2 | a0015c0031t0002g0321 a0021c0026t0001g0132 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4094-923A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740211 | |||||||
chr15:48740502 | C | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(299): Show |
315 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.4093+1099G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740502 | |||||||
chr15:48740588 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4093+1013C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740588 | |||||||
chr15:48740615 | C | CT | 86 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0037 others(83): Show |
91 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.4093+985dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | |||||||
chr15:48740615 | C | CTT | 13 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0138 others(10): Show |
13 | HG01952.hp1 HG02717.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.4093+984_4093+985d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | |||||||
chr15:48740615 | CT | C | 10 | a0001c0001t0001g0078 a0001c0001t0001g0125 a0001c0001t0001g0180 others(7): Show |
10 | HG00642.hp1 HG01069.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.4093+985delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740615 | |||||||
chr15:48740807 | TG | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(69): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.4093+793delC | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740807 | |||||||
chr15:48740851 | T | C | 1 | a0001c0001t0002g0304 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4093+750A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740851 | |||||||
chr15:48740931 | A | G | 6 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.4093+670T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740931 | |||||||
chr15:48740956 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(75): Show |
81 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.4093+645T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740956 | |||||||
chr15:48740987 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4093+614G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48740987 | |||||||
chr15:48741028 | A | T | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(183): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.4093+573T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741028 | |||||||
chr15:48741088 | C | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.4093+513G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741088 | |||||||
chr15:48741118 | A | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.4093+483T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741118 | |||||||
chr15:48741130 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0216 others(7): Show |
11 | HG00738.hp2 HG01071.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4093+462_4093+470d others(11): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | |||||||
chr15:48741130 | C | CTTTTTTT others(3): Show |
148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(145): Show |
157 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.4093+461_4093+470d others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | |||||||
chr15:48741130 | C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0017 a0001c0001t0001g0061 a0001c0001t0001g0090 others(23): Show |
26 | HG00140.hp2 HG01099.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.4093+460_4093+470d others(13): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741130 | |||||||
chr15:48741412 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4093+189A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741412 | |||||||
chr15:48741567 | T | C | 1 | a0001c0016t0004g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4093+34A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741567 | |||||||
chr15:48741600 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA19070.hp2 | splice_donor_variant&intron_variant | HIGH | c.4093+1G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 26/26 | chr15 | 48741600 | |||||||
chr15:48742195 | T | C | 1 | a0017c0039t0002g0256 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3836-95A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742195 | |||||||
chr15:48742260 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3836-160T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742260 | |||||||
chr15:48742307 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3836-207G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742307 | |||||||
chr15:48742308 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3836-208C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742308 | |||||||
chr15:48742640 | T | C | 3 | a0001c0001t0001g0226 a0002c0002t0002g0001 a0002c0002t0002g0264 |
6 | NA18953.hp1 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.3836-540A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742640 | |||||||
chr15:48742709 | C | T | 2 | a0026c0032t0001g0148 a0028c0028t0002g0286 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3836-609G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742709 | |||||||
chr15:48742810 | A | AT | 8 | a0001c0024t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0252 others(5): Show |
9 | HG02258.hp1 NA18942.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.3836-711dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742810 | |||||||
chr15:48742824 | T | G | 55 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(52): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3836-724A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742824 | |||||||
chr15:48742842 | C | G | 2 | a0003c0003t0001g0211 a0029c0030t0001g0207 |
2 | NA18962.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3836-742G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742842 | |||||||
chr15:48742987 | A | C | 2 | a0001c0001t0001g0190 a0001c0014t0001g0178 |
2 | NA19010.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3836-887T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48742987 | |||||||
chr15:48743051 | A | G | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3836-951T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743051 | |||||||
chr15:48743094 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3836-994T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743094 | |||||||
chr15:48743548 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3835+692G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743548 | |||||||
chr15:48743563 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3835+677A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743563 | |||||||
chr15:48743769 | T | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(186): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.3835+471A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48743769 | |||||||
chr15:48744050 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3835+190A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744050 | |||||||
chr15:48744148 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3835+92C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744148 | |||||||
chr15:48744220 | A | C | 2 | a0026c0032t0001g0148 a0028c0028t0002g0286 |
2 | NA19000.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3835+20T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 24/26 | chr15 | 48744220 | |||||||
chr15:48744705 | T | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3731+191A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/26 | chr15 | 48744705 | |||||||
chr15:48744764 | T | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3731+132A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 23/26 | chr15 | 48744764 | |||||||
chr15:48745116 | G | A | 1 | a0002c0002t0006g0266 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3635-124C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745116 | |||||||
chr15:48745266 | A | G | 1 | a0003c0003t0002g0296 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3635-274T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745266 | |||||||
chr15:48745319 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3635-327T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745319 | |||||||
chr15:48745434 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3635-442A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745434 | |||||||
chr15:48745452 | T | TTG | 3 | a0003c0003t0001g0160 a0003c0003t0001g0170 a0003c0003t0002g0294 |
3 | NA18963.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3635-462_3635-461d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745452 | |||||||
chr15:48745452 | TTG | T | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(178): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.3635-462_3635-461d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745452 | |||||||
chr15:48745732 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(69): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3635-740C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745732 | |||||||
chr15:48745943 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3635-951A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745943 | |||||||
chr15:48745954 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3635-962C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745954 | |||||||
chr15:48745984 | C | T | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3635-992G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48745984 | |||||||
chr15:48746033 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0058 |
2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.3635-1041G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746033 | |||||||
chr15:48746159 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3635-1167T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746159 | |||||||
chr15:48746273 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(69): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.3635-1281G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746273 | |||||||
chr15:48746486 | A | G | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3635-1494T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746486 | |||||||
chr15:48746501 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3635-1509G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746501 | |||||||
chr15:48746502 | A | G | 2 | a0001c0024t0001g0136 a0014c0018t0001g0232 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3635-1510T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746502 | |||||||
chr15:48746559 | G | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3635-1567C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746559 | |||||||
chr15:48746655 | T | C | 2 | a0001c0024t0001g0136 a0014c0018t0001g0232 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3635-1663A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746655 | |||||||
chr15:48746671 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
8 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3635-1679C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48746671 | |||||||
chr15:48747029 | G | C | 1 | a0002c0002t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3634+1414C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747029 | |||||||
chr15:48747275 | G | C | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1168C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747275 | |||||||
chr15:48747288 | T | C | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1155A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747288 | |||||||
chr15:48747294 | C | G | 1 | a0018c0027t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3634+1149G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747294 | |||||||
chr15:48747336 | T | C | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1107A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747336 | |||||||
chr15:48747344 | A | G | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3634+1099T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747344 | |||||||
chr15:48747429 | G | T | 1 | a0004c0004t0001g0146 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3634+1014C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747429 | |||||||
chr15:48747513 | G | A | 1 | a0006c0006t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3634+930C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747513 | |||||||
chr15:48747572 | A | G | 1 | a0001c0001t0002g0308 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3634+871T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747572 | |||||||
chr15:48747600 | T | C | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(183): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.3634+843A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747600 | |||||||
chr15:48747685 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3634+758T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747685 | |||||||
chr15:48747879 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3634+564C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747879 | |||||||
chr15:48747908 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3634+535A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747908 | |||||||
chr15:48747934 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3634+509C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747934 | |||||||
chr15:48747976 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3634+467G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48747976 | |||||||
chr15:48748082 | T | A | 1 | a0008c0011t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3634+361A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748082 | |||||||
chr15:48748104 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3634+339A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748104 | |||||||
chr15:48748303 | T | G | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3634+140A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748303 | |||||||
chr15:48748322 | A | C | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3634+121T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 22/26 | chr15 | 48748322 | |||||||
chr15:48748667 | TA | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.3467-58delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48748667 | |||||||
chr15:48749238 | A | C | 3 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0297 |
3 | NA18957.hp2 NA18985.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.3467-628T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749238 | |||||||
chr15:48749556 | A | G | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3467-946T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749556 | |||||||
chr15:48749584 | A | G | 4 | a0004c0004t0001g0139 a0004c0004t0001g0144 a0004c0004t0001g0145 others(1): Show |
4 | NA18949.hp1 NA19058.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.3467-974T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749584 | |||||||
chr15:48749837 | GA | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(26): Show |
31 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.3467-1228delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48749837 | |||||||
chr15:48750015 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
48 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.3467-1405G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750015 | |||||||
chr15:48750070 | A | G | 1 | a0002c0002t0002g0251 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3467-1460T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750070 | |||||||
chr15:48750481 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3466+1868A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750481 | |||||||
chr15:48750647 | C | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3466+1702G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750647 | |||||||
chr15:48750664 | T | C | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+1685A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750664 | |||||||
chr15:48750721 | C | T | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3466+1628G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750721 | |||||||
chr15:48750722 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.3466+1627T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750722 | |||||||
chr15:48750814 | A | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3466+1535T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750814 | |||||||
chr15:48750820 | T | C | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3466+1529A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750820 | |||||||
chr15:48750965 | G | C | 1 | a0004c0004t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3466+1384C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48750965 | |||||||
chr15:48751063 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+1286G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751063 | |||||||
chr15:48751196 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3466+1153T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751196 | |||||||
chr15:48751351 | A | G | 1 | a0002c0002t0002g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3466+998T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751351 | |||||||
chr15:48751352 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+997C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751352 | |||||||
chr15:48751516 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3466+833C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751516 | |||||||
chr15:48751568 | G | A | 1 | a0012c0013t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3466+781C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751568 | |||||||
chr15:48751652 | C | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(123): Show |
132 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.3466+697G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751652 | |||||||
chr15:48751652 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+697G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751652 | |||||||
chr15:48751777 | C | G | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3466+572G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751777 | |||||||
chr15:48751792 | T | C | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3466+557A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751792 | |||||||
chr15:48751805 | C | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
47 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.3466+544G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48751805 | |||||||
chr15:48752239 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3466+110G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48752239 | |||||||
chr15:48752341 | C | G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
splice_region_variant&intron_variant | LOW | c.3466+8G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 21/26 | chr15 | 48752341 | |||||||
chr15:48752619 | T | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0082 others(6): Show |
9 | HG00621.hp2 NA18747.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.3346-150A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752619 | |||||||
chr15:48752730 | G | C | 1 | a0001c0001t0002g0291 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3346-261C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752730 | |||||||
chr15:48752850 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG00140.hp1 HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3346-381C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752850 | |||||||
chr15:48752880 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3346-411G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48752880 | |||||||
chr15:48753328 | A | G | 1 | a0004c0004t0001g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3346-859T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753328 | |||||||
chr15:48753483 | C | G | 1 | a0001c0001t0002g0319 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3346-1014G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753483 | |||||||
chr15:48753567 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
46 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.3346-1098G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753567 | |||||||
chr15:48753670 | A | G | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3346-1201T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48753670 | |||||||
chr15:48754526 | C | CA | 6 | a0007c0012t0001g0062 a0007c0012t0001g0075 a0007c0017t0001g0026 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3345+1376dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754526 | |||||||
chr15:48754561 | G | A | 1 | a0021c0026t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3345+1342C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754561 | |||||||
chr15:48754597 | G | T | 4 | a0005c0005t0001g0043 a0005c0005t0001g0049 a0005c0005t0001g0051 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+1306C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754597 | |||||||
chr15:48754680 | T | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1223A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754680 | |||||||
chr15:48754762 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1141G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754762 | |||||||
chr15:48754852 | G | A | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+1051C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754852 | |||||||
chr15:48754970 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3345+933G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48754970 | |||||||
chr15:48755017 | CT | C | 55 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(52): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+885delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755017 | |||||||
chr15:48755074 | C | G | 1 | a0015c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3345+829G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755074 | |||||||
chr15:48755134 | A | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(186): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.3345+769T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755134 | |||||||
chr15:48755134 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0013 |
3 | NA18977.hp1 NA19081.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3345+769T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755134 | |||||||
chr15:48755145 | C | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3345+758G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755145 | |||||||
chr15:48755147 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3345+756C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755147 | |||||||
chr15:48755157 | T | A | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3345+746A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755157 | |||||||
chr15:48755266 | G | A | 55 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(52): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+637C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755266 | |||||||
chr15:48755275 | G | A | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+628C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755275 | |||||||
chr15:48755295 | A | G | 55 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(52): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+608T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755295 | |||||||
chr15:48755468 | T | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3345+435A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755468 | |||||||
chr15:48755793 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3345+110T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755793 | |||||||
chr15:48755810 | T | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3345+93A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 20/26 | chr15 | 48755810 | |||||||
chr15:48756768 | G | C | 51 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(48): Show |
55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2695-215C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48756768 | |||||||
chr15:48757007 | T | C | 1 | a0001c0009t0005g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2695-454A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757007 | |||||||
chr15:48757148 | C | G | 1 | a0004c0004t0001g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2695-595G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757148 | |||||||
chr15:48757154 | C | CA | 56 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(53): Show |
60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.2695-602dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757154 | |||||||
chr15:48757218 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2695-665C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757218 | |||||||
chr15:48757492 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2695-939G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757492 | |||||||
chr15:48757603 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2695-1050G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757603 | |||||||
chr15:48757626 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.2695-1073G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757626 | |||||||
chr15:48757734 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0060 |
2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2695-1181T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757734 | |||||||
chr15:48757769 | G | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2695-1216C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757769 | |||||||
chr15:48757782 | A | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(138): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2695-1229T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757782 | |||||||
chr15:48757970 | T | C | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2695-1417A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48757970 | |||||||
chr15:48758131 | T | A | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2695-1578A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758131 | |||||||
chr15:48758252 | C | T | 1 | a0002c0002t0006g0266 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2695-1699G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758252 | |||||||
chr15:48758279 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2695-1726A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758279 | |||||||
chr15:48758446 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2694+1689C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758446 | |||||||
chr15:48758587 | C | T | 1 | a0011c0015t0001g0140 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2694+1548G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758587 | |||||||
chr15:48758677 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2694+1458G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758677 | |||||||
chr15:48758718 | C | CAA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0121 others(22): Show |
27 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.2694+1415_2694+141 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758718 | C | CAAA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(73): Show |
79 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.2694+1414_2694+141 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758718 | C | CAAAA | 36 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0065 others(33): Show |
36 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2694+1413_2694+141 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758718 | C | CAAAAAAA | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(81): Show |
88 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2694+1410_2694+141 others(11): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758718 | C | CAAAAAAA others(1): Show |
42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(39): Show |
44 | HG00408.hp2 HG01123.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.2694+1409_2694+141 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758718 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2694+1405_2694+141 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758718 | |||||||
chr15:48758773 | T | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+1362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758773 | |||||||
chr15:48758901 | A | G | 1 | a0021c0026t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2694+1234T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758901 | |||||||
chr15:48758976 | A | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+1159T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48758976 | |||||||
chr15:48759106 | G | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(187): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2694+1029C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759106 | |||||||
chr15:48759442 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2694+693A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759442 | |||||||
chr15:48759453 | C | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2694+682G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759453 | |||||||
chr15:48759457 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2694+678A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759457 | |||||||
chr15:48759646 | T | C | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2694+489A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759646 | |||||||
chr15:48759715 | C | G | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2694+420G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759715 | |||||||
chr15:48759752 | A | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2694+383T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 19/26 | chr15 | 48759752 | |||||||
chr15:48760336 | G | C | 1 | a0006c0006t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2563-70C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760336 | |||||||
chr15:48760472 | A | C | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2563-206T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760472 | |||||||
chr15:48760612 | A | G | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
40 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.2563-346T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760612 | |||||||
chr15:48760614 | T | C | 1 | a0021c0026t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2563-348A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760614 | |||||||
chr15:48760632 | C | T | 50 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(47): Show |
54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2563-366G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760632 | |||||||
chr15:48760704 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2563-438T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760704 | |||||||
chr15:48760999 | G | C | 7 | a0001c0001t0002g0249 a0001c0001t0002g0295 a0002c0002t0002g0243 others(4): Show |
7 | NA18955.hp1 NA18956.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.2563-733C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48760999 | |||||||
chr15:48761053 | T | G | 51 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(48): Show |
55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2563-787A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761053 | |||||||
chr15:48761214 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0189 a0001c0001t0001g0198 others(1): Show |
4 | HG00099.hp1 HG00642.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2563-948C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761214 | |||||||
chr15:48761243 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2563-977T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761243 | |||||||
chr15:48761381 | T | C | 3 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0016t0004g0108 |
3 | HG00099.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2562+1010A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761381 | |||||||
chr15:48761649 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2562+742G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761649 | |||||||
chr15:48761786 | A | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2562+605T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48761786 | |||||||
chr15:48762290 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2562+101T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 18/26 | chr15 | 48762290 | |||||||
chr15:48762755 | C | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
46 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.2281-83G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762755 | |||||||
chr15:48762909 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2281-237A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762909 | |||||||
chr15:48762965 | T | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(74): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2281-293A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762965 | |||||||
chr15:48762989 | T | TA | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(125): Show |
134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2281-318dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48762989 | |||||||
chr15:48763034 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2281-362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763034 | |||||||
chr15:48763098 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2281-426C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763098 | |||||||
chr15:48763138 | G | A | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2281-466C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763138 | |||||||
chr15:48763214 | C | T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2281-542G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763214 | |||||||
chr15:48763263 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2281-591A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763263 | |||||||
chr15:48763404 | T | G | 1 | a0004c0004t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2281-732A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763404 | |||||||
chr15:48763509 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2281-837T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763509 | |||||||
chr15:48763640 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2281-968G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763640 | |||||||
chr15:48763690 | A | AT | 3 | a0003c0003t0001g0159 a0003c0003t0001g0160 a0003c0003t0001g0170 |
3 | HG02080.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2281-1019dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763690 | |||||||
chr15:48763917 | T | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(27): Show |
32 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.2281-1245A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763917 | |||||||
chr15:48763994 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2281-1322A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48763994 | |||||||
chr15:48764047 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2281-1375G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764047 | |||||||
chr15:48764092 | A | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(186): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2281-1420T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764092 | |||||||
chr15:48764473 | T | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(187): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2281-1801A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764473 | |||||||
chr15:48764607 | G | A | 1 | a0002c0002t0002g0258 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2281-1935C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764607 | |||||||
chr15:48764937 | C | T | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+2123G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764937 | |||||||
chr15:48764942 | C | G | 1 | a0004c0004t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2280+2118G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764942 | |||||||
chr15:48764992 | TA | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0147 a0002c0002t0002g0250 others(3): Show |
6 | HG00597.hp2 HG01257.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2280+2067delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48764992 | |||||||
chr15:48765056 | C | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(180): Show |
193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2280+2004G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765056 | |||||||
chr15:48765066 | A | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2280+1994T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765066 | |||||||
chr15:48765279 | C | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(184): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.2280+1781G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765279 | |||||||
chr15:48765424 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2280+1636A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765424 | |||||||
chr15:48765471 | T | C | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+1589A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765471 | |||||||
chr15:48765546 | A | G | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2280+1514T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765546 | |||||||
chr15:48765636 | A | AT | 52 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0031 others(49): Show |
57 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2280+1423dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATT | 40 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0056 others(37): Show |
40 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2280+1422_2280+142 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTT | 8 | a0001c0001t0001g0103 a0001c0001t0002g0295 a0001c0001t0002g0297 others(5): Show |
8 | HG02886.hp1 HG03516.hp1 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.2280+1421_2280+142 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0090 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2280+1420_2280+142 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0098 a0001c0001t0002g0288 a0007c0012t0001g0075 |
3 | HG03041.hp1 HG03486.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2280+1412_2280+142 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0287 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2280+1411_2280+142 others(17): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2280+1407_2280+142 others(21): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0106 |
4 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280+1406_2280+142 others(22): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2280+1405_2280+142 others(23): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2280+1402_2280+142 others(26): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2280+1400_2280+142 others(28): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | AT | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2280+1423delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATT | A | 21 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0063 others(18): Show |
21 | HG00544.hp2 HG00558.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2280+1422_2280+142 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTT | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0222 others(3): Show |
6 | HG02922.hp1 HG03209.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.2280+1421_2280+142 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTTT | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(12): Show |
17 | HG00408.hp2 HG01884.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.2280+1420_2280+142 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2280+1410_2280+142 others(18): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTTTTTT others(10): Show |
A | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+1407_2280+142 others(21): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTTTTTT others(11): Show |
A | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2280+1406_2280+142 others(22): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765636 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2280+1404_2280+142 others(24): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765636 | |||||||
chr15:48765699 | G | C | 1 | a0002c0002t0002g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2280+1361C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765699 | |||||||
chr15:48765802 | C | T | 1 | a0002c0002t0002g0281 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2280+1258G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765802 | |||||||
chr15:48765873 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2280+1187G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765873 | |||||||
chr15:48765995 | T | C | 39 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0065 others(36): Show |
39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2280+1065A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48765995 | |||||||
chr15:48766201 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2280+859G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766201 | |||||||
chr15:48766639 | C | T | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2280+421G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766639 | |||||||
chr15:48766787 | C | CT | 9 | a0001c0001t0002g0295 a0001c0001t0002g0318 a0002c0002t0002g0012 others(6): Show |
10 | HG03225.hp2 HG03927.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2280+272dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48766787 | |||||||
chr15:48767029 | G | T | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2280+31C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 17/26 | chr15 | 48767029 | |||||||
chr15:48767476 | C | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(39): Show |
45 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.2019-13G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767476 | |||||||
chr15:48767506 | C | T | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2019-43G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767506 | |||||||
chr15:48767571 | T | C | 2 | a0015c0031t0002g0321 a0021c0026t0001g0132 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2019-108A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767571 | |||||||
chr15:48767745 | T | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2019-282A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767745 | |||||||
chr15:48767804 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2019-341A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767804 | |||||||
chr15:48767886 | G | T | 50 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(47): Show |
54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2018+333C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767886 | |||||||
chr15:48767947 | C | T | 1 | a0001c0016t0004g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2018+272G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767947 | |||||||
chr15:48767969 | C | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(188): Show |
201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.2018+250G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767969 | |||||||
chr15:48767973 | T | C | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2018+246A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48767973 | |||||||
chr15:48768088 | C | G | 2 | a0015c0031t0002g0321 a0021c0026t0001g0132 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2018+131G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 15/26 | chr15 | 48768088 | |||||||
chr15:48768336 | C | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02615.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.1909-8G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768336 | |||||||
chr15:48768355 | C | T | 1 | a0005c0005t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1909-27G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768355 | |||||||
chr15:48768489 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1909-161C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768489 | |||||||
chr15:48768528 | T | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(184): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1909-200A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768528 | |||||||
chr15:48768591 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1909-263A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768591 | |||||||
chr15:48768645 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1908+311A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768645 | |||||||
chr15:48768733 | T | C | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1908+223A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768733 | |||||||
chr15:48768790 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1908+166G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768790 | |||||||
chr15:48768929 | TAA | T | 4 | a0003c0003t0001g0046 a0003c0003t0001g0141 a0003c0003t0001g0228 others(1): Show |
4 | HG02056.hp1 NA18985.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+25_1908+26del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768929 | |||||||
chr15:48768933 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1908+23T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 14/26 | chr15 | 48768933 | |||||||
chr15:48769104 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0064 |
2 | NA18948.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1783-23A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769104 | |||||||
chr15:48769111 | A | G | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1783-30T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769111 | |||||||
chr15:48769114 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0064 |
2 | NA18948.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1783-33A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769114 | |||||||
chr15:48769171 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1783-90G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769171 | |||||||
chr15:48769199 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1783-118T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769199 | |||||||
chr15:48769249 | T | C | 1 | a0002c0002t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1783-168A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769249 | |||||||
chr15:48769295 | T | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-214A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769295 | |||||||
chr15:48769408 | A | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-327T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769408 | |||||||
chr15:48769458 | G | A | 321 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1783-377C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769458 | |||||||
chr15:48769508 | A | C | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1783-427T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769508 | |||||||
chr15:48769551 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1783-470C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769551 | |||||||
chr15:48769696 | A | G | 57 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(54): Show |
61 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1783-615T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769696 | |||||||
chr15:48769778 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1783-697C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769778 | |||||||
chr15:48769783 | T | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1783-702A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48769783 | |||||||
chr15:48770273 | C | T | 1 | a0003c0003t0001g0161 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1783-1192G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770273 | |||||||
chr15:48770489 | CA | C | 50 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(47): Show |
54 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1783-1409delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770489 | |||||||
chr15:48770918 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1782+1569A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770918 | |||||||
chr15:48770959 | A | AAAAG | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1782+1527_1782+152 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770959 | |||||||
chr15:48770987 | G | A | 1 | a0018c0027t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1782+1500C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770987 | |||||||
chr15:48770993 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1782+1494T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48770993 | |||||||
chr15:48771027 | T | C | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(178): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1782+1460A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771027 | |||||||
chr15:48771232 | T | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(73): Show |
79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1782+1255A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771232 | |||||||
chr15:48771271 | CAA | C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
131 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1782+1214_1782+121 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771271 | |||||||
chr15:48771336 | G | C | 1 | a0002c0002t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1782+1151C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771336 | |||||||
chr15:48771344 | A | T | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1782+1143T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771344 | |||||||
chr15:48771457 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
48 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.1782+1030C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48771457 | |||||||
chr15:48772154 | G | A | 3 | a0007c0012t0001g0062 a0007c0012t0001g0075 a0015c0031t0002g0321 |
3 | HG01891.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1782+333C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772154 | |||||||
chr15:48772175 | T | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1782+312A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772175 | |||||||
chr15:48772275 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1782+212C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772275 | |||||||
chr15:48772325 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(116): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1782+162G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772325 | |||||||
chr15:48772429 | A | C | 6 | a0001c0001t0001g0171 a0001c0001t0001g0213 a0001c0001t0001g0219 others(3): Show |
6 | HG02015.hp1 NA18942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+58T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 13/26 | chr15 | 48772429 | |||||||
chr15:48772697 | G | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0064 |
3 | NA18948.hp1 NA18961.hp2 NA18984.hp1 |
splice_region_variant&intron_variant | LOW | c.1578-6C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48772697 | |||||||
chr15:48773259 | A | C | 2 | a0007c0012t0001g0062 a0007c0012t0001g0075 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1578-568T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773259 | |||||||
chr15:48773346 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1578-655C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773346 | |||||||
chr15:48773441 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1578-750G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773441 | |||||||
chr15:48773492 | T | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(120): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1578-801A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773492 | |||||||
chr15:48773561 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1578-870C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773561 | |||||||
chr15:48773586 | A | T | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1578-895T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773586 | |||||||
chr15:48773837 | A | G | 1 | a0003c0003t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1578-1146T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773837 | |||||||
chr15:48773881 | T | C | 55 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(52): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1578-1190A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48773881 | |||||||
chr15:48774005 | T | C | 1 | a0015c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1578-1314A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774005 | |||||||
chr15:48774080 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-1389A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774080 | |||||||
chr15:48774428 | T | C | 1 | a0006c0006t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1578-1737A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774428 | |||||||
chr15:48774455 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1578-1764C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774455 | |||||||
chr15:48774471 | G | A | 1 | a0009c0008t0001g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1578-1780C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774471 | |||||||
chr15:48774484 | C | A | 1 | a0001c0001t0004g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1578-1793G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774484 | |||||||
chr15:48774523 | C | T | 1 | a0003c0003t0001g0228 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1578-1832G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774523 | |||||||
chr15:48774705 | C | CTG | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-2015_1578-201 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774705 | |||||||
chr15:48774793 | A | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1578-2102T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48774793 | |||||||
chr15:48775140 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1578-2449T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775140 | |||||||
chr15:48775525 | A | G | 1 | a0015c0031t0002g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1578-2834T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775525 | |||||||
chr15:48775559 | T | C | 1 | a0002c0002t0002g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1578-2868A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775559 | |||||||
chr15:48775588 | T | A | 1 | a0001c0001t0001g0036 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1578-2897A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775588 | |||||||
chr15:48775663 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1578-2972T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775663 | |||||||
chr15:48775664 | T | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(120): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1578-2973A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775664 | |||||||
chr15:48775724 | T | A | 51 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(48): Show |
55 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1578-3033A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775724 | |||||||
chr15:48775780 | T | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1578-3089A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775780 | |||||||
chr15:48775922 | TA | T | 324 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(321): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1578-3232delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775922 | |||||||
chr15:48775946 | C | T | 2 | a0001c0001t0001g0037 a0002c0002t0002g0280 |
2 | NA18990.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1578-3255G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48775946 | |||||||
chr15:48776039 | G | GAA | 56 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(53): Show |
60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578-3350_1578-334 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776039 | |||||||
chr15:48776137 | C | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-3446G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776137 | |||||||
chr15:48776161 | A | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-3470T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776161 | |||||||
chr15:48776484 | C | A | 1 | a0002c0002t0002g0271 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1578-3793G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776484 | |||||||
chr15:48776582 | T | C | 2 | a0001c0001t0001g0186 a0009c0008t0001g0187 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1578-3891A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776582 | |||||||
chr15:48776888 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0105 |
2 | HG01169.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1578-4197C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776888 | |||||||
chr15:48776913 | T | C | 2 | a0002c0002t0002g0254 a0002c0002t0002g0269 |
2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1578-4222A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776913 | |||||||
chr15:48776994 | G | A | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(183): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1577+4202C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48776994 | |||||||
chr15:48777138 | A | C | 1 | a0027c0019t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1577+4058T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777138 | |||||||
chr15:48777198 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1577+3998A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777198 | |||||||
chr15:48777308 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+3888C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777308 | |||||||
chr15:48777325 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1577+3871C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777325 | |||||||
chr15:48777466 | T | TTG | 8 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0004g0127 others(5): Show |
8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1577+3728_1577+372 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTG | 12 | a0001c0001t0001g0163 a0001c0001t0001g0215 a0001c0001t0001g0216 others(9): Show |
12 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.1577+3726_1577+372 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTG | 33 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
36 | HG00408.hp2 HG01109.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.1577+3724_1577+372 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTGT others(1): Show |
37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(34): Show |
40 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1577+3722_1577+372 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTGT others(3): Show |
23 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0057 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.1577+3720_1577+372 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0042 a0001c0001t0001g0110 a0001c0001t0002g0316 others(5): Show |
8 | HG00323.hp1 HG01106.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1577+3718_1577+372 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTGT others(7): Show |
3 | a0001c0001t0002g0302 a0001c0001t0002g0303 a0001c0001t0002g0307 |
3 | HG02155.hp1 NA18949.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1577+3716_1577+372 others(18): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | T | TTGTGTGT others(9): Show |
1 | a0002c0002t0002g0258 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1577+3714_1577+372 others(20): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | TTG | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(128): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1577+3728_1577+372 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777466 | TTGTGTG | T | 4 | a0001c0001t0001g0076 a0003c0003t0002g0294 a0014c0018t0001g0232 others(1): Show |
4 | HG01884.hp1 HG02074.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1577+3724_1577+372 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777466 | |||||||
chr15:48777515 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1577+3681G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777515 | |||||||
chr15:48777637 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1577+3559T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777637 | |||||||
chr15:48777638 | T | C | 1 | a0009c0008t0001g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1577+3558A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777638 | |||||||
chr15:48777703 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1577+3493A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777703 | |||||||
chr15:48777848 | G | A | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1577+3348C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777848 | |||||||
chr15:48777995 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1577+3201A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48777995 | |||||||
chr15:48778405 | C | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(120): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1577+2791G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778405 | |||||||
chr15:48778467 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1577+2729C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778467 | |||||||
chr15:48778616 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0128 others(3): Show |
8 | HG00140.hp1 HG00280.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1577+2580G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778616 | |||||||
chr15:48778672 | G | A | 5 | a0007c0012t0001g0062 a0007c0012t0001g0075 a0007c0017t0001g0026 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1577+2524C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778672 | |||||||
chr15:48778674 | G | T | 1 | a0002c0002t0002g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1577+2522C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778674 | |||||||
chr15:48778677 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+2519G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778677 | |||||||
chr15:48778715 | C | T | 9 | a0001c0001t0001g0163 a0001c0001t0002g0287 a0001c0001t0002g0288 others(6): Show |
9 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1577+2481G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778715 | |||||||
chr15:48778779 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02451.hp2 HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1577+2417C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778779 | |||||||
chr15:48778852 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1577+2344C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778852 | |||||||
chr15:48778949 | C | CA | 17 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1577+2246dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778949 | |||||||
chr15:48778965 | G | C | 17 | a0001c0001t0001g0085 a0001c0001t0001g0133 a0001c0001t0001g0176 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1577+2231C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48778965 | |||||||
chr15:48779010 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1577+2186C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779010 | |||||||
chr15:48779348 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1577+1848T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779348 | |||||||
chr15:48779613 | C | A | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+1583G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779613 | |||||||
chr15:48779639 | G | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(26): Show |
31 | HG00408.hp2 HG01109.hp1 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1577+1557C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779639 | |||||||
chr15:48779884 | C | A | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+1312G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779884 | |||||||
chr15:48779930 | G | A | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1577+1266C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48779930 | |||||||
chr15:48780277 | G | A | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+919C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780277 | |||||||
chr15:48780483 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1577+713A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780483 | |||||||
chr15:48780583 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0002g0322 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1577+613A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780583 | |||||||
chr15:48780590 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0002g0322 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1577+606A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780590 | |||||||
chr15:48780780 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0023c0035t0001g0071 |
3 | NA18943.hp1 NA18962.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1577+416G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780780 | |||||||
chr15:48780830 | C | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(120): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1577+366G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780830 | |||||||
chr15:48780838 | G | A | 1 | a0004c0004t0001g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1577+358C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48780838 | |||||||
chr15:48781052 | C | G | 1 | a0011c0015t0001g0140 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1577+144G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781052 | |||||||
chr15:48781080 | A | G | 2 | a0001c0001t0004g0127 a0001c0001t0004g0134 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1577+116T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781080 | |||||||
chr15:48781099 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0123 others(20): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1577+97A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781099 | |||||||
chr15:48781190 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG01496.hp1 HG02257.hp1 HG02280.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1577+6G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 12/26 | chr15 | 48781190 | |||||||
chr15:48781706 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(188): Show |
201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1414-347T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781706 | |||||||
chr15:48781719 | G | C | 17 | a0001c0001t0001g0085 a0001c0001t0001g0133 a0001c0001t0001g0176 others(14): Show |
17 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1414-360C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781719 | |||||||
chr15:48781726 | G | T | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1414-367C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781726 | |||||||
chr15:48781799 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0002g0326 |
2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1413+340A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781799 | |||||||
chr15:48781895 | G | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0147 a0002c0002t0002g0250 others(2): Show |
5 | HG00597.hp2 HG02129.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413+244C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781895 | |||||||
chr15:48781938 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1413+201C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781938 | |||||||
chr15:48781996 | G | A | 1 | a0003c0003t0001g0157 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1413+143C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48781996 | |||||||
chr15:48782034 | G | C | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1413+105C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 11/26 | chr15 | 48782034 | |||||||
chr15:48782342 | C | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1322-112G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782342 | |||||||
chr15:48782505 | C | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(116): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1322-275G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782505 | |||||||
chr15:48782667 | C | T | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1322-437G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782667 | |||||||
chr15:48782721 | AT | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0063 others(1): Show |
4 | NA18948.hp1 NA18961.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1322-492delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782721 | |||||||
chr15:48782818 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1322-588T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782818 | |||||||
chr15:48782967 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1322-737G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48782967 | |||||||
chr15:48783032 | T | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(72): Show |
78 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1322-802A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783032 | |||||||
chr15:48783263 | G | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(116): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1321+710C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783263 | |||||||
chr15:48783479 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1321+494A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783479 | |||||||
chr15:48783506 | G | C | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0006c0006t0001g0025 |
3 | HG01884.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1321+467C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783506 | |||||||
chr15:48783621 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1321+352G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783621 | |||||||
chr15:48783706 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1321+267A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783706 | |||||||
chr15:48783721 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0123 others(20): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1321+252A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783721 | |||||||
chr15:48783775 | G | GTA | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(141): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1321+196_1321+197d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | |||||||
chr15:48783775 | G | GTATA | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(34): Show |
39 | HG00408.hp2 HG01109.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.1321+194_1321+197d others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | |||||||
chr15:48783775 | G | GTATATA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
8 | HG02717.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1321+192_1321+197d others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783775 | |||||||
chr15:48783791 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0002g0255 |
3 | HG02738.hp1 NA18971.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.1321+182C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783791 | |||||||
chr15:48783892 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1321+81A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 10/26 | chr15 | 48783892 | |||||||
chr15:48784379 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1174-259T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784379 | |||||||
chr15:48784476 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0002g0326 |
2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-356A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784476 | |||||||
chr15:48784482 | T | C | 5 | a0007c0012t0001g0062 a0007c0012t0001g0075 a0007c0017t0001g0026 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-362A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784482 | |||||||
chr15:48784529 | A | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-409T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784529 | |||||||
chr15:48784589 | C | T | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174-469G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784589 | |||||||
chr15:48784721 | C | A | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | NA18961.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1174-601G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784721 | |||||||
chr15:48784882 | T | C | 3 | a0003c0003t0001g0159 a0003c0003t0001g0160 a0003c0003t0001g0170 |
3 | HG02080.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1174-762A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48784882 | |||||||
chr15:48785231 | G | C | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1174-1111C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785231 | |||||||
chr15:48785266 | T | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1146A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785266 | |||||||
chr15:48785406 | T | TCTCAAG | 5 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0001t0004g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1287_1174-128 others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785406 | |||||||
chr15:48785619 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1174-1499A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785619 | |||||||
chr15:48785732 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1174-1612A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785732 | |||||||
chr15:48785864 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1174-1744G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785864 | |||||||
chr15:48785918 | AAAGAG | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(114): Show |
123 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1174-1803_1174-179 others(9): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785918 | |||||||
chr15:48785919 | AAGAG | A | 3 | a0001c0001t0001g0226 a0002c0002t0002g0001 a0002c0002t0002g0264 |
6 | NA18953.hp1 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-1803_1174-180 others(8): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785919 | |||||||
chr15:48785984 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1174-1864C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48785984 | |||||||
chr15:48786026 | A | C | 3 | a0001c0001t0004g0048 a0001c0001t0004g0083 a0001c0016t0004g0108 |
3 | HG00099.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1174-1906T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786026 | |||||||
chr15:48786062 | AGT | A | 48 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0037 others(45): Show |
52 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1174-1944_1174-194 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786062 | |||||||
chr15:48786314 | A | C | 1 | a0001c0001t0001g0047 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1174-2194T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786314 | |||||||
chr15:48786385 | C | CA | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1174-2266dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786385 | |||||||
chr15:48786606 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1173+2195G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786606 | |||||||
chr15:48786685 | A | AAAT | 29 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0090 others(26): Show |
30 | HG00735.hp2 HG01981.hp2 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+2113_1173+211 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786685 | |||||||
chr15:48786769 | G | A | 37 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0124 others(34): Show |
37 | HG00140.hp2 HG00621.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.1173+2032C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786769 | |||||||
chr15:48786948 | A | T | 4 | a0002c0002t0002g0012 a0002c0002t0002g0272 a0002c0002t0002g0276 others(1): Show |
5 | NA18952.hp1 NA18964.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1853T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786948 | |||||||
chr15:48786993 | C | G | 1 | a0001c0009t0005g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+1808G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48786993 | |||||||
chr15:48787156 | A | C | 2 | a0014c0018t0001g0232 a0019c0025t0001g0231 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1173+1645T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787156 | |||||||
chr15:48787163 | G | GTTTTTTG others(1): Show |
14 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(11): Show |
14 | HG01175.hp2 HG01978.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1173+1637_1173+163 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTG others(3): Show |
2 | a0001c0001t0001g0186 a0009c0008t0001g0187 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1173+1637_1173+163 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTT others(1): Show |
29 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0065 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1173+1630_1173+163 others(12): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTT others(2): Show |
72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1173+1629_1173+163 others(13): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTT others(3): Show |
18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(15): Show |
18 | HG00621.hp2 HG01106.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1173+1628_1173+163 others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1173+1627_1173+163 others(15): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | G | GTTTTTTT others(5): Show |
1 | a0006c0006t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+1626_1173+163 others(16): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | GT | G | 88 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0037 others(85): Show |
94 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1173+1637delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787163 | GTT | G | 71 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0102 others(68): Show |
73 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1173+1636_1173+163 others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787163 | |||||||
chr15:48787172 | T | G | 1 | a0001c0001t0002g0307 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1173+1629A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787172 | |||||||
chr15:48787182 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1173+1619A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787182 | |||||||
chr15:48787232 | A | G | 1 | a0006c0006t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1173+1569T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787232 | |||||||
chr15:48787264 | C | CTTG | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+1536_1173+153 others(7): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787264 | |||||||
chr15:48787352 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1173+1449C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787352 | |||||||
chr15:48787386 | G | A | 1 | a0027c0019t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1173+1415C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787386 | |||||||
chr15:48787400 | G | A | 1 | a0002c0002t0002g0272 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1173+1401C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787400 | |||||||
chr15:48787461 | G | A | 1 | a0025c0020t0001g0069 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1173+1340C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787461 | |||||||
chr15:48787729 | AC | A | 40 | a0002c0002t0002g0001 a0002c0002t0002g0012 a0002c0002t0002g0243 others(37): Show |
44 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1173+1071delG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48787729 | |||||||
chr15:48788084 | C | T | 8 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0289 others(5): Show |
8 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+717G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788084 | |||||||
chr15:48788118 | T | C | 2 | a0003c0003t0001g0032 a0003c0003t0001g0033 |
2 | NA18992.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1173+683A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788118 | |||||||
chr15:48788148 | A | C | 9 | a0001c0001t0002g0249 a0001c0001t0002g0287 a0001c0001t0002g0288 others(6): Show |
9 | HG01952.hp2 HG01978.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1173+653T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788148 | |||||||
chr15:48788326 | CT | C | 104 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0114 others(101): Show |
110 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1173+474delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788326 | |||||||
chr15:48788326 | CTT | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
156 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1173+473_1173+474d others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788326 | |||||||
chr15:48788330 | T | C | 1 | a0002c0002t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1173+471A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788330 | |||||||
chr15:48788373 | G | A | 2 | a0001c0001t0001g0077 a0006c0006t0001g0020 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+428C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788373 | |||||||
chr15:48788423 | T | G | 2 | a0001c0001t0004g0134 a0020c0021t0001g0135 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1173+378A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788423 | |||||||
chr15:48788427 | G | A | 1 | a0003c0003t0001g0228 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1173+374C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788427 | |||||||
chr15:48788480 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1173+321G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788480 | |||||||
chr15:48788701 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1173+100T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 9/26 | chr15 | 48788701 | |||||||
chr15:48789135 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0003g0235 |
2 | HG02293.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.973-134G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789135 | |||||||
chr15:48789182 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.973-181G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789182 | |||||||
chr15:48789315 | G | GC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.973-315dupG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789315 | |||||||
chr15:48789340 | A | G | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.973-339T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789340 | |||||||
chr15:48789342 | G | A | 1 | a0003c0003t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.973-341C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789342 | |||||||
chr15:48789659 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.973-658A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789659 | |||||||
chr15:48789944 | C | T | 1 | a0003c0003t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.973-943G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48789944 | |||||||
chr15:48790518 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | HG01496.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.972+719T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790518 | |||||||
chr15:48790550 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+687G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790550 | |||||||
chr15:48790652 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+585G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790652 | |||||||
chr15:48790733 | A | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0092 |
3 | HG00323.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.972+504T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790733 | |||||||
chr15:48790825 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.972+412G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790825 | |||||||
chr15:48790853 | C | G | 1 | a0006c0006t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972+384G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790853 | |||||||
chr15:48790854 | C | A | 1 | a0006c0006t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972+383G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790854 | |||||||
chr15:48790987 | T | C | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.972+250A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48790987 | |||||||
chr15:48791001 | C | T | 41 | a0002c0002t0002g0001 a0002c0002t0002g0012 a0002c0002t0002g0243 others(38): Show |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.972+236G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 8/26 | chr15 | 48791001 | |||||||
chr15:48791380 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
splice_region_variant&intron_variant | LOW | c.833-4G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791380 | |||||||
chr15:48791421 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.833-45C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791421 | |||||||
chr15:48791677 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.833-301G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791677 | |||||||
chr15:48791830 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.833-454A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48791830 | |||||||
chr15:48792061 | C | G | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-685G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792061 | |||||||
chr15:48792477 | C | T | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.832+844G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792477 | |||||||
chr15:48792690 | A | G | 3 | a0006c0006t0001g0020 a0006c0006t0001g0025 a0007c0017t0001g0026 |
3 | HG01884.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.832+631T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792690 | |||||||
chr15:48792783 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+538T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792783 | |||||||
chr15:48792815 | A | T | 1 | a0002c0002t0002g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.832+506T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792815 | |||||||
chr15:48792820 | C | CT | 9 | a0001c0001t0001g0129 a0001c0001t0001g0205 a0002c0002t0002g0248 others(6): Show |
9 | HG01069.hp1 HG01081.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+500dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 7/26 | chr15 | 48792820 | |||||||
chr15:48793613 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18984.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.692-152T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48793613 | |||||||
chr15:48793629 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.692-168G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48793629 | |||||||
chr15:48794203 | A | T | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.692-742T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794203 | |||||||
chr15:48794252 | A | T | 1 | a0001c0001t0003g0236 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.692-791T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794252 | |||||||
chr15:48794267 | A | G | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(4): Show |
7 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.692-806T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794267 | |||||||
chr15:48794675 | T | C | 16 | a0001c0001t0001g0147 a0001c0001t0001g0233 a0003c0003t0001g0141 others(13): Show |
17 | HG00558.hp2 HG00597.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.692-1214A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794675 | |||||||
chr15:48794802 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.691+1208C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794802 | |||||||
chr15:48794999 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.691+1011C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48794999 | |||||||
chr15:48795145 | A | G | 1 | a0001c0001t0002g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.691+865T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795145 | |||||||
chr15:48795419 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.691+591A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795419 | |||||||
chr15:48795440 | T | C | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.691+570A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795440 | |||||||
chr15:48795596 | C | T | 41 | a0002c0002t0002g0001 a0002c0002t0002g0012 a0002c0002t0002g0243 others(38): Show |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.691+414G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795596 | |||||||
chr15:48795737 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.691+273A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48795737 | |||||||
chr15:48796001 | G | A | 14 | a0001c0001t0001g0176 a0001c0001t0001g0191 a0001c0001t0001g0193 others(11): Show |
14 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.691+9C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 6/26 | chr15 | 48796001 | |||||||
chr15:48796197 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.541-37G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796197 | |||||||
chr15:48796280 | T | TTA | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02895.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.541-122_541-121dup others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796280 | |||||||
chr15:48796287 | TATAC | T | 42 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.541-131_541-128del others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | |||||||
chr15:48796287 | TATACACA others(3): Show |
T | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.541-137_541-128del others(10): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | |||||||
chr15:48796287 | TATACACA others(7): Show |
T | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.541-141_541-128del others(14): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796287 | |||||||
chr15:48796289 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0001g0192 |
3 | HG01981.hp1 HG02886.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.541-129A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | |||||||
chr15:48796289 | T | TAC | 18 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
20 | HG00140.hp1 HG00280.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.541-131_541-130dup others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | |||||||
chr15:48796289 | TAC | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
23 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.541-131_541-130del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | |||||||
chr15:48796289 | TACAC | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
167 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.541-133_541-130del others(4): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | |||||||
chr15:48796289 | TACACAC | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0085 a0002c0002t0002g0250 others(1): Show |
4 | HG01123.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-135_541-130del others(6): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796289 | |||||||
chr15:48796291 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-131G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796291 | |||||||
chr15:48796295 | C | T | 37 | a0001c0001t0003g0235 a0002c0002t0002g0001 a0002c0002t0002g0012 others(34): Show |
41 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.541-135G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796295 | |||||||
chr15:48796297 | C | T | 2 | a0002c0002t0002g0250 a0002c0002t0002g0276 |
2 | HG04204.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.541-137G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796297 | |||||||
chr15:48796316 | A | C | 1 | a0001c0001t0002g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.541-156T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796316 | |||||||
chr15:48796325 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0002g0319 |
2 | HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.541-165A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796325 | |||||||
chr15:48796356 | G | A | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541-196C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796356 | |||||||
chr15:48796399 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.541-239A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796399 | |||||||
chr15:48796487 | T | A | 1 | a0001c0001t0002g0314 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.541-327A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796487 | |||||||
chr15:48796843 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.540+458T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796843 | |||||||
chr15:48796851 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540+450A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48796851 | |||||||
chr15:48797220 | T | C | 1 | a0002c0002t0002g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.540+81A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797220 | |||||||
chr15:48797227 | C | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.540+74G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797227 | |||||||
chr15:48797248 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.540+53G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 5/26 | chr15 | 48797248 | |||||||
chr15:48797910 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.191+38T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797910 | |||||||
chr15:48797927 | A | C | 1 | a0001c0001t0002g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.191+21T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797927 | |||||||
chr15:48797937 | C | T | 16 | a0001c0001t0001g0147 a0001c0001t0001g0233 a0003c0003t0001g0141 others(13): Show |
17 | HG00558.hp2 HG00597.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.191+11G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 3/26 | chr15 | 48797937 | |||||||
chr15:48798157 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.88-106G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798157 | |||||||
chr15:48798261 | CT | C | 48 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0107 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.88-211delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798261 | |||||||
chr15:48798430 | T | C | 1 | a0004c0004t0001g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.88-379A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798430 | |||||||
chr15:48798540 | CT | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.88-490delA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798540 | |||||||
chr15:48798846 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-795G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798846 | |||||||
chr15:48798916 | TATA | T | 40 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0173 others(37): Show |
40 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-868_88-866delTA others(1): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48798916 | |||||||
chr15:48799106 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.88-1055A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799106 | |||||||
chr15:48799160 | G | GA | 33 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
36 | HG00408.hp2 HG01109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.88-1110dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799160 | |||||||
chr15:48799307 | T | C | 2 | a0001c0009t0005g0022 a0001c0009t0005g0023 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88-1256A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799307 | |||||||
chr15:48799484 | A | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.88-1433T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799484 | |||||||
chr15:48799617 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.88-1566A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799617 | |||||||
chr15:48799982 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.88-1931T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48799982 | |||||||
chr15:48800052 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88-2001G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800052 | |||||||
chr15:48800119 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0004g0134 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-2068G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800119 | |||||||
chr15:48800156 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 others(1): Show |
4 | HG02698.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-2105C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800156 | |||||||
chr15:48800224 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88-2173A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800224 | |||||||
chr15:48800646 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.88-2595G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48800646 | |||||||
chr15:48801104 | T | C | 2 | a0014c0018t0001g0232 a0019c0025t0001g0231 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.88-3053A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801104 | |||||||
chr15:48801403 | G | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88-3352C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801403 | |||||||
chr15:48801440 | A | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0016t0004g0108 others(1): Show |
4 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-3389T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801440 | |||||||
chr15:48801627 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.88-3576A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801627 | |||||||
chr15:48801738 | G | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.88-3687C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801738 | |||||||
chr15:48801808 | C | A | 1 | a0001c0001t0002g0319 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.87+3755G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801808 | |||||||
chr15:48801952 | C | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG01175.hp2 HG01978.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.87+3611G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48801952 | |||||||
chr15:48802022 | G | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0138 others(36): Show |
41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.87+3541C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802022 | |||||||
chr15:48802032 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.87+3531C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802032 | |||||||
chr15:48802052 | T | C | 1 | a0007c0012t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.87+3511A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802052 | |||||||
chr15:48802066 | G | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0138 others(36): Show |
41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.87+3497C>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802066 | |||||||
chr15:48802197 | G | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.87+3366C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802197 | |||||||
chr15:48802358 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.87+3205T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802358 | |||||||
chr15:48802367 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.87+3196C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802367 | |||||||
chr15:48802437 | C | A | 1 | a0001c0001t0002g0326 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.87+3126G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802437 | |||||||
chr15:48802446 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87+3117G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802446 | |||||||
chr15:48802637 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.87+2926A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802637 | |||||||
chr15:48802670 | G | A | 42 | a0002c0002t0002g0001 a0002c0002t0002g0012 a0002c0002t0002g0243 others(39): Show |
46 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.87+2893C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802670 | |||||||
chr15:48802754 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.87+2809G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802754 | |||||||
chr15:48802821 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.87+2742A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48802821 | |||||||
chr15:48803005 | T | G | 15 | a0001c0001t0001g0176 a0001c0001t0001g0191 a0001c0001t0001g0192 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.87+2558A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803005 | |||||||
chr15:48803170 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.87+2393G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803170 | |||||||
chr15:48803670 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG01243.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+1893A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803670 | |||||||
chr15:48803819 | A | G | 2 | a0006c0006t0001g0025 a0007c0017t0001g0026 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.87+1744T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48803819 | |||||||
chr15:48804103 | T | C | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.87+1460A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804103 | |||||||
chr15:48804181 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+1382A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804181 | |||||||
chr15:48804377 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.87+1186C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804377 | |||||||
chr15:48804452 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.87+1111A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804452 | |||||||
chr15:48804463 | A | G | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.87+1100T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804463 | |||||||
chr15:48804489 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.87+1074C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804489 | |||||||
chr15:48804608 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.87+955G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804608 | |||||||
chr15:48804818 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.87+745T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804818 | |||||||
chr15:48804859 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.87+704T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804859 | |||||||
chr15:48804878 | C | A | 41 | a0002c0002t0002g0001 a0002c0002t0002g0012 a0002c0002t0002g0243 others(38): Show |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.87+685G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48804878 | |||||||
chr15:48805037 | A | G | 1 | a0001c0024t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+526T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805037 | |||||||
chr15:48805438 | G | GT | 42 | a0001c0001t0002g0249 a0002c0002t0002g0001 a0002c0002t0002g0012 others(39): Show |
46 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.87+124dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805438 | |||||||
chr15:48805439 | T | G | 1 | a0020c0021t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.87+124A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805439 | |||||||
chr15:48805448 | T | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(28): Show |
34 | HG00408.hp2 HG01109.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.87+115A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805448 | |||||||
chr15:48805449 | A | T | 4 | a0001c0001t0001g0031 a0003c0003t0001g0030 a0003c0003t0001g0032 others(1): Show |
4 | HG02027.hp1 HG02040.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+114T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805449 | |||||||
chr15:48805535 | C | CT | 116 | a0001c0001t0001g0013 a0001c0001t0001g0102 a0001c0001t0001g0103 others(113): Show |
122 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.87+27dupA | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805535 | |||||||
chr15:48805536 | T | TC | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
98 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.87+26_87+27insG | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805536 | |||||||
chr15:48805537 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(28): Show |
34 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.87+26A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805537 | |||||||
chr15:48805538 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.87+25A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 2/26 | chr15 | 48805538 | |||||||
chr15:48805819 | C | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-7-163G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48805819 | |||||||
chr15:48805825 | T | C | 5 | a0001c0001t0002g0315 a0001c0001t0002g0316 a0001c0001t0002g0317 others(2): Show |
5 | HG00140.hp2 HG01099.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-169A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48805825 | |||||||
chr15:48806483 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-827G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806483 | |||||||
chr15:48806506 | T | A | 1 | a0014c0018t0001g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7-850A>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806506 | |||||||
chr15:48806558 | G | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0138 others(36): Show |
41 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-7-902C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806558 | |||||||
chr15:48806690 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-7-1034G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806690 | |||||||
chr15:48806964 | G | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0212 others(18): Show |
23 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7-1308C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806964 | |||||||
chr15:48806992 | T | C | 1 | a0019c0025t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-1336A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48806992 | |||||||
chr15:48807561 | C | CA | 18 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
18 | HG00323.hp2 HG00642.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-1906dupT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | |||||||
chr15:48807561 | CA | C | 149 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(146): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-7-1906delT | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | |||||||
chr15:48807561 | CAA | C | 42 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-7-1907_-7-1906del others(2): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807561 | |||||||
chr15:48807718 | C | T | 41 | a0001c0001t0002g0249 a0002c0002t0002g0001 a0002c0002t0002g0012 others(38): Show |
45 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-7-2062G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807718 | |||||||
chr15:48807782 | T | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0138 others(37): Show |
42 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-7-2126A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807782 | |||||||
chr15:48807904 | T | TTAAAG | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-7-2253_-7-2249dup others(5): Show |
CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807904 | |||||||
chr15:48807932 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-7-2276T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48807932 | |||||||
chr15:48808083 | C | A | 1 | a0003c0003t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-7-2427G>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808083 | |||||||
chr15:48808513 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG01175.hp2 HG01978.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-8+2448G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808513 | |||||||
chr15:48808546 | A | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0212 others(20): Show |
25 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+2415T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808546 | |||||||
chr15:48808785 | G | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
2 | NA18957.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-8+2176C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808785 | |||||||
chr15:48808956 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2005T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808956 | |||||||
chr15:48808983 | C | T | 2 | a0001c0001t0001g0233 a0014c0018t0001g0232 |
2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+1978G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48808983 | |||||||
chr15:48809005 | T | C | 2 | a0001c0001t0001g0233 a0014c0018t0001g0232 |
2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+1956A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809005 | |||||||
chr15:48809008 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-8+1953G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809008 | |||||||
chr15:48809077 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-8+1884T>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809077 | |||||||
chr15:48809272 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-8+1689A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809272 | |||||||
chr15:48809294 | T | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-8+1667A>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809294 | |||||||
chr15:48809312 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+1649G>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809312 | |||||||
chr15:48809610 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8+1351A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809610 | |||||||
chr15:48809634 | G | A | 40 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0173 others(37): Show |
40 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-8+1327C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809634 | |||||||
chr15:48809693 | G | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0016t0004g0108 others(2): Show |
5 | HG00099.hp2 HG00323.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+1268C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809693 | |||||||
chr15:48809799 | A | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(8): Show |
12 | HG01169.hp2 HG02717.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+1162T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809799 | |||||||
chr15:48809840 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-8+1121C>T | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809840 | |||||||
chr15:48809938 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8+1023T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48809938 | |||||||
chr15:48810130 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-8+831T>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810130 | |||||||
chr15:48810183 | T | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0212 others(18): Show |
23 | HG00408.hp2 HG01109.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+778A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810183 | |||||||
chr15:48810190 | T | C | 3 | a0001c0001t0001g0233 a0014c0018t0001g0232 a0019c0025t0001g0231 |
3 | HG01884.hp1 HG02451.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+771A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810190 | |||||||
chr15:48810468 | G | T | 2 | a0008c0011t0001g0094 a0008c0011t0001g0095 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-8+493C>A | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810468 | |||||||
chr15:48810622 | T | C | 3 | a0001c0001t0001g0233 a0014c0018t0001g0232 a0019c0025t0001g0231 |
3 | HG01884.hp1 HG02451.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-8+339A>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810622 | |||||||
chr15:48810688 | C | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-8+273G>C | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810688 | |||||||
chr15:48810703 | A | C | 1 | a0001c0001t0001g0013 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-8+258T>G | CEP152 | ENSG00000103995.14 | transcript | ENST00000380950.7 | protein_coding | 1/26 | chr15 | 48810703 |