Item | Value |
---|---|
geneid | 55125 |
ensemblid | ENSG00000101639.19 |
hgncid | 25515 |
symbol | CEP192 |
name | centrosomal protein 192 |
refseq_nuc | NM_032142.4 |
refseq_prot | NP_115518.3 |
ensembl_nuc | ENST00000506447.5 |
ensembl_prot | ENSP00000427550.1 |
mane_status | MANE Select |
chr | chr18 |
start | 12991362 |
end | 13125036 |
strand | + |
ver | v1.2 |
region | chr18:12991362-13125036 |
region5000 | chr18:12986362-13130036 |
regionname0 | CEP192_chr18_12991362_13125036 |
regionname5000 | CEP192_chr18_12986362_13130036 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2537 | 74 | 6 | 6 | 50 | 1 | 11 | 38 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0002 | 0/0 | 2537 | 71 | 10 | 17 | 32 | 5 | 7 | 22 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0003 | 1/1 | 2537 | 63 | 3 | 17 | 23 | 4 | 14 | 17 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0004 | 0/0 | 2537 | 50 | 0 | 2 | 44 | 0 | 4 | 36 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0005 | 0/0 | 2537 | 47 | 21 | 4 | 15 | 2 | 5 | 12 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0006 | 0/0 | 2537 | 12 | 10 | 0 | 0 | 1 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0007 | 0/0 | 2536 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2531): Show |
chr18 | 12986362 | 13130036 |
a0008 | 0/0 | 2537 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0009 | 0/0 | 2537 | 7 | 1 | 0 | 6 | 0 | 0 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0010 | 0/0 | 2537 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0011 | 0/0 | 2537 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0012 | 0/0 | 2537 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0013 | 0/0 | 2537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0014 | 0/0 | 2537 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0015 | 0/0 | 2537 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0016 | 0/0 | 2537 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0017 | 0/0 | 2537 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0018 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0019 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0020 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0021 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0022 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0023 | 0/0 | 2537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0024 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0025 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0026 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0027 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0028 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0029 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0030 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0031 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0032 | 0/0 | 2537 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0033 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0034 | 0/0 | 2537 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0035 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
a0036 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | MEDFR others(2532): Show |
chr18 | 12986362 | 13130036 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 7611 | 69 | 5 | 6 | 47 | 1 | 10 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0001c0033 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0001c0034 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0001c0036 | 0/0 | 7611 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0001c0040 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0001c0044 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0002c0001 | 0/0 | 7611 | 69 | 10 | 16 | 31 | 5 | 7 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0002c0022 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0002c0023 | 0/0 | 7611 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0003c0003 | 1/1 | 7611 | 63 | 3 | 17 | 23 | 4 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0004c0004 | 0/0 | 7611 | 50 | 0 | 2 | 44 | 0 | 4 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0005c0005 | 0/0 | 7611 | 47 | 21 | 4 | 15 | 2 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0006c0006 | 0/0 | 7611 | 12 | 10 | 0 | 0 | 1 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0007c0007 | 0/0 | 7608 | 10 | 9 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7603): Show |
chr18 | 12986362 | 13130036 | ||
a0008c0008 | 0/0 | 7611 | 8 | 8 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0009c0009 | 0/0 | 7611 | 7 | 1 | 0 | 6 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0010c0010 | 0/0 | 7611 | 7 | 0 | 7 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0011c0011 | 0/0 | 7611 | 5 | 3 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0012c0013 | 0/0 | 7611 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0012c0039 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0013c0016 | 0/0 | 7611 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0013c0029 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0014c0012 | 0/0 | 7611 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0015c0014 | 0/0 | 7611 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0016c0018 | 0/0 | 7611 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0017c0017 | 0/0 | 7611 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0018c0019 | 0/0 | 7611 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0019c0015 | 0/0 | 7611 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0020c0025 | 0/0 | 7611 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0021c0026 | 0/0 | 7611 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0022c0021 | 0/0 | 7611 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0023c0027 | 0/0 | 7611 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0024c0042 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0025c0031 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0026c0038 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0027c0045 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0028c0043 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0029c0020 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0030c0041 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0031c0030 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0032c0037 | 0/0 | 7611 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0033c0024 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0034c0032 | 0/0 | 7611 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0035c0028 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 | ||
a0036c0035 | 0/0 | 7611 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | ATGGA others(7606): Show |
chr18 | 12986362 | 13130036 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 7960 | 68 | 5 | 6 | 47 | 1 | 9 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0002t0005 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0033t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0034t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0036t0001 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0040t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0001c0044t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0002c0001t0001 | 0/0 | 7960 | 69 | 10 | 16 | 31 | 5 | 7 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0002c0022t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0002c0023t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0003c0003t0002 | 1/1 | 7960 | 62 | 3 | 17 | 22 | 4 | 14 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0003c0003t0006 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0004c0004t0001 | 0/0 | 7960 | 49 | 0 | 2 | 43 | 0 | 4 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0004c0004t0004 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0005c0005t0001 | 0/0 | 7960 | 47 | 21 | 4 | 15 | 2 | 5 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0006c0006t0001 | 0/0 | 7960 | 2 | 0 | 0 | 0 | 1 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0006c0006t0002 | 0/0 | 7960 | 10 | 10 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0007c0007t0002 | 0/0 | 7957 | 10 | 9 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7952): Show |
chr18 | 12986362 | 13130036 |
a0008c0008t0001 | 0/0 | 7960 | 8 | 8 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0009c0009t0001 | 0/0 | 7960 | 7 | 1 | 0 | 6 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0010c0010t0002 | 0/0 | 7960 | 7 | 0 | 7 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0011c0011t0001 | 0/0 | 7960 | 5 | 3 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0012c0013t0002 | 0/0 | 7960 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0012c0039t0002 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0013c0016t0003 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0013c0029t0003 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0014c0012t0001 | 0/0 | 7960 | 3 | 3 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0015c0014t0001 | 0/0 | 7960 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0016c0018t0002 | 0/0 | 7960 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0017c0017t0002 | 0/0 | 7960 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0018c0019t0001 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0019c0015t0002 | 0/0 | 7960 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0020c0025t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0021c0026t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0022c0021t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0023c0027t0001 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0024c0042t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0025c0031t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0026c0038t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0027c0045t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0028c0043t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0029c0020t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0030c0041t0002 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0031c0030t0001 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0032c0037t0002 | 0/0 | 7960 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0033c0024t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0034c0032t0001 | 0/0 | 7960 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0035c0028t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
a0036c0035t0001 | 0/0 | 7960 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | AGTGC others(7955): Show |
chr18 | 12986362 | 13130036 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0033t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0034t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0036t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0040t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0001c0044t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0022t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0002c0023t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0003c0003t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0004c0004t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0005c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0006c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0007c0007t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0008c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0009c0009t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0009c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0009c0009t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0009c0009t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0010c0010t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0011c0011t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0011c0011t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0011c0011t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0011c0011t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0011c0011t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0012c0013t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0012c0013t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0012c0013t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0012c0039t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0013c0016t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0013c0016t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0013c0029t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0014c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0014c0012t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0014c0012t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0015c0014t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0015c0014t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0016c0018t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0016c0018t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0017c0017t0002g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0018c0019t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0018c0019t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0019c0015t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0019c0015t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0020c0025t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0021c0026t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0022c0021t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0023c0027t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0024c0042t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0025c0031t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0026c0038t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0027c0045t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0028c0043t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0029c0020t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0030c0041t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0031c0030t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0032c0037t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0033c0024t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0034c0032t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0035c0028t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
a0036c0035t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0002 | g0089 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00099 | hp2 | a0005 | c0005 | t0001 | g0136 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0296 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00140 | hp2 | a0003 | c0003 | t0002 | g0102 | EUR | GBR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0281 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0057 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00323 | hp1 | a0003 | c0003 | t0002 | g0056 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00323 | hp2 | a0002 | c0001 | t0001 | g0343 | EUR | FIN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00408 | hp2 | a0004 | c0004 | t0001 | g0117 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00423 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0330 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00438 | hp1 | a0004 | c0004 | t0001 | g0119 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0347 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0299 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0074 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00558 | hp2 | a0004 | c0004 | t0004 | g0176 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00597 | hp1 | a0005 | c0005 | t0001 | g0284 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00597 | hp2 | a0003 | c0003 | t0002 | g0073 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00609 | hp1 | a0004 | c0004 | t0001 | g0185 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0300 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00621 | hp1 | a0004 | c0004 | t0001 | g0199 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00621 | hp2 | a0009 | c0009 | t0001 | g0003 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00639 | hp1 | a0002 | c0023 | t0001 | g0291 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0059 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00642 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0322 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0285 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00735 | hp2 | a0003 | c0003 | t0002 | g0053 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00738 | hp1 | a0020 | c0025 | t0001 | g0295 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00738 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0293 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG00741 | hp2 | a0003 | c0003 | t0002 | g0110 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0288 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01069 | hp2 | a0003 | c0003 | t0002 | g0008 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0008 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01071 | hp2 | a0005 | c0005 | t0001 | g0116 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0065 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0286 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01099 | hp1 | a0002 | c0001 | t0001 | g0352 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01099 | hp2 | a0005 | c0005 | t0001 | g0134 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01109 | hp1 | a0021 | c0026 | t0001 | g0294 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01109 | hp2 | a0022 | c0021 | t0001 | g0346 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01167 | hp1 | a0005 | c0005 | t0001 | g0124 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01167 | hp2 | a0011 | c0011 | t0001 | g0283 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01168 | hp1 | a0010 | c0010 | t0002 | g0111 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01169 | hp1 | a0011 | c0011 | t0001 | g0282 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01169 | hp2 | a0010 | c0010 | t0002 | g0112 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01192 | hp1 | a0023 | c0027 | t0001 | g0342 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01255 | hp1 | a0005 | c0005 | t0001 | g0127 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01255 | hp2 | a0003 | c0003 | t0002 | g0100 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01256 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0304 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01258 | hp1 | a0003 | c0003 | t0002 | g0011 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01258 | hp2 | a0010 | c0010 | t0002 | g0103 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01261 | hp2 | a0003 | c0003 | t0002 | g0060 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0305 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01361 | hp2 | a0004 | c0004 | t0001 | g0180 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01496 | hp1 | a0003 | c0003 | t0002 | g0072 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0290 | AMR | CLM | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01515 | hp1 | a0006 | c0006 | t0001 | g0357 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01515 | hp2 | a0016 | c0018 | t0002 | g0091 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01516 | hp1 | a0005 | c0005 | t0001 | g0147 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0021 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01517 | hp1 | a0016 | c0018 | t0002 | g0061 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01517 | hp2 | a0002 | c0001 | t0001 | g0021 | EUR | IBS | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01884 | hp1 | a0005 | c0005 | t0001 | g0162 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01884 | hp2 | a0005 | c0005 | t0001 | g0158 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01891 | hp1 | a0008 | c0008 | t0001 | g0132 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01891 | hp2 | a0006 | c0006 | t0002 | g0041 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01928 | hp1 | a0002 | c0001 | t0001 | g0311 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01928 | hp2 | a0010 | c0010 | t0002 | g0078 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01952 | hp1 | a0003 | c0003 | t0002 | g0071 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01952 | hp2 | a0007 | c0007 | t0002 | g0027 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0055 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0313 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01981 | hp1 | a0010 | c0010 | t0002 | g0080 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01981 | hp2 | a0004 | c0004 | t0001 | g0174 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0323 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG01993 | hp2 | a0010 | c0010 | t0002 | g0079 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02004 | hp2 | a0010 | c0010 | t0002 | g0047 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02015 | hp1 | a0005 | c0005 | t0001 | g0126 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0345 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0324 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02071 | hp1 | a0005 | c0005 | t0001 | g0016 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0298 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02074 | hp1 | a0003 | c0003 | t0002 | g0049 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0309 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02080 | hp1 | a0017 | c0017 | t0002 | g0010 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02083 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02129 | hp1 | a0003 | c0003 | t0002 | g0044 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02132 | hp1 | a0024 | c0042 | t0001 | g0140 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02145 | hp1 | a0012 | c0039 | t0002 | g0104 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02145 | hp2 | a0008 | c0008 | t0001 | g0168 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02257 | hp1 | a0017 | c0017 | t0002 | g0010 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02257 | hp2 | a0006 | c0006 | t0002 | g0026 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02258 | hp1 | a0006 | c0006 | t0002 | g0036 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02258 | hp2 | a0013 | c0029 | t0003 | g0214 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02273 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02280 | hp1 | a0006 | c0006 | t0002 | g0043 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02280 | hp2 | a0003 | c0003 | t0002 | g0085 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02293 | hp2 | a0002 | c0001 | t0001 | g0318 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02300 | hp1 | a0003 | c0003 | t0002 | g0098 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02451 | hp1 | a0005 | c0005 | t0001 | g0133 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0325 | EAS | KHV | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02572 | hp1 | a0001 | c0044 | t0001 | g0268 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02572 | hp2 | a0008 | c0008 | t0001 | g0129 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02615 | hp1 | a0014 | c0012 | t0001 | g0012 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02615 | hp2 | a0007 | c0007 | t0002 | g0029 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02622 | hp1 | a0025 | c0031 | t0001 | g0012 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02622 | hp2 | a0007 | c0007 | t0002 | g0025 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02630 | hp1 | a0008 | c0008 | t0001 | g0128 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02630 | hp2 | a0005 | c0005 | t0001 | g0122 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02647 | hp1 | a0006 | c0006 | t0002 | g0037 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02647 | hp2 | a0005 | c0005 | t0001 | g0145 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02683 | hp2 | a0003 | c0003 | t0002 | g0058 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0292 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02698 | hp2 | a0003 | c0003 | t0002 | g0082 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02717 | hp1 | a0026 | c0038 | t0001 | g0151 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02717 | hp2 | a0008 | c0008 | t0001 | g0131 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02723 | hp1 | a0006 | c0006 | t0002 | g0035 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02723 | hp2 | a0011 | c0011 | t0001 | g0335 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0331 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02735 | hp2 | a0003 | c0003 | t0002 | g0086 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02738 | hp2 | a0003 | c0003 | t0002 | g0105 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02818 | hp1 | a0007 | c0007 | t0002 | g0007 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02818 | hp2 | a0005 | c0005 | t0001 | g0163 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0157 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02886 | hp2 | a0008 | c0008 | t0001 | g0146 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02895 | hp1 | a0019 | c0015 | t0002 | g0040 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02896 | hp1 | a0014 | c0012 | t0001 | g0114 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02896 | hp2 | a0007 | c0007 | t0002 | g0030 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02897 | hp1 | a0014 | c0012 | t0001 | g0113 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02897 | hp2 | a0019 | c0015 | t0002 | g0039 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02922 | hp1 | a0007 | c0007 | t0002 | g0006 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02922 | hp2 | a0027 | c0045 | t0001 | g0333 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02965 | hp1 | a0012 | c0013 | t0002 | g0083 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02965 | hp2 | a0006 | c0006 | t0002 | g0033 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0340 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02976 | hp2 | a0018 | c0019 | t0001 | g0165 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03041 | hp1 | a0002 | c0001 | t0001 | g0337 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03041 | hp2 | a0013 | c0016 | t0003 | g0215 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03098 | hp1 | a0005 | c0005 | t0001 | g0153 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03098 | hp2 | a0012 | c0013 | t0002 | g0108 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03130 | hp1 | a0005 | c0005 | t0001 | g0161 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03130 | hp2 | a0007 | c0007 | t0002 | g0024 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03139 | hp1 | a0028 | c0043 | t0001 | g0164 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03139 | hp2 | a0006 | c0006 | t0002 | g0034 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03195 | hp1 | a0005 | c0005 | t0001 | g0152 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03195 | hp2 | a0002 | c0001 | t0001 | g0336 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03209 | hp1 | a0008 | c0008 | t0001 | g0130 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0360 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03225 | hp1 | a0007 | c0007 | t0002 | g0006 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03225 | hp2 | a0002 | c0001 | t0001 | g0338 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03239 | hp1 | a0005 | c0005 | t0001 | g0138 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03239 | hp2 | a0006 | c0006 | t0001 | g0355 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03453 | hp1 | a0013 | c0016 | t0003 | g0216 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03453 | hp2 | a0011 | c0011 | t0001 | g0353 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03486 | hp1 | a0006 | c0006 | t0002 | g0038 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03486 | hp2 | a0005 | c0005 | t0001 | g0150 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03491 | hp1 | a0002 | c0001 | t0001 | g0287 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03491 | hp2 | a0001 | c0036 | t0001 | g0222 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03492 | hp1 | a0003 | c0003 | t0002 | g0051 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03492 | hp2 | a0002 | c0001 | t0001 | g0289 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0359 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03516 | hp2 | a0008 | c0008 | t0001 | g0167 | AFR | ESN | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03540 | hp1 | a0005 | c0005 | t0001 | g0159 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0123 | AFR | GWD | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03579 | hp1 | a0002 | c0001 | t0001 | g0020 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0339 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03654 | hp1 | a0005 | c0005 | t0001 | g0115 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0237 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03669 | hp1 | a0005 | c0005 | t0001 | g0141 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03669 | hp2 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03688 | hp1 | a0003 | c0003 | t0002 | g0075 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0205 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03704 | hp2 | a0005 | c0005 | t0001 | g0160 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0344 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03710 | hp2 | a0004 | c0004 | t0001 | g0179 | SAS | PJL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03831 | hp1 | a0003 | c0003 | t0002 | g0097 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03834 | hp1 | a0005 | c0005 | t0001 | g0135 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03927 | hp2 | a0003 | c0003 | t0002 | g0076 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0054 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04184 | hp1 | a0003 | c0003 | t0002 | g0095 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | BEB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04199 | hp1 | a0004 | c0004 | t0001 | g0173 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04199 | hp2 | a0003 | c0003 | t0002 | g0052 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04204 | hp1 | a0003 | c0003 | t0002 | g0062 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04204 | hp2 | a0002 | c0001 | t0001 | g0308 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0297 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0081 | SAS | STU | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18522 | hp1 | a0009 | c0009 | t0001 | g0219 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18612 | hp1 | a0003 | c0003 | t0002 | g0093 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0189 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18747 | hp2 | a0004 | c0004 | t0001 | g0208 | EAS | CHB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18906 | hp1 | a0012 | c0013 | t0002 | g0096 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18906 | hp2 | a0007 | c0007 | t0002 | g0007 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18940 | hp2 | a0002 | c0001 | t0001 | g0349 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18941 | hp1 | a0005 | c0005 | t0001 | g0139 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18941 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18942 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18944 | hp1 | a0015 | c0014 | t0001 | g0013 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18944 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0307 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18946 | hp2 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18947 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18947 | hp2 | a0030 | c0041 | t0002 | g0106 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18949 | hp1 | a0004 | c0004 | t0001 | g0204 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18949 | hp2 | a0002 | c0022 | t0001 | g0302 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18950 | hp1 | a0001 | c0040 | t0001 | g0241 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18950 | hp2 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18954 | hp1 | a0009 | c0009 | t0001 | g0217 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0329 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18956 | hp2 | a0005 | c0005 | t0001 | g0170 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18959 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18961 | hp1 | a0004 | c0004 | t0001 | g0202 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18962 | hp1 | a0003 | c0003 | t0002 | g0077 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0191 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18964 | hp1 | a0004 | c0004 | t0001 | g0182 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18964 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18965 | hp1 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0328 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18966 | hp1 | a0005 | c0005 | t0001 | g0014 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18966 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18967 | hp1 | a0003 | c0003 | t0002 | g0090 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0201 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18968 | hp2 | a0003 | c0003 | t0006 | g0099 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18969 | hp1 | a0003 | c0003 | t0002 | g0066 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0321 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18970 | hp1 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18971 | hp1 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18974 | hp1 | a0004 | c0004 | t0001 | g0177 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18975 | hp1 | a0004 | c0004 | t0001 | g0196 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18977 | hp1 | a0031 | c0030 | t0001 | g0175 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18977 | hp2 | a0005 | c0005 | t0001 | g0169 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0348 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18979 | hp2 | a0032 | c0037 | t0002 | g0069 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18980 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18981 | hp1 | a0001 | c0033 | t0001 | g0210 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18981 | hp2 | a0004 | c0004 | t0001 | g0181 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18982 | hp1 | a0005 | c0005 | t0001 | g0144 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18982 | hp2 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18983 | hp1 | a0015 | c0014 | t0001 | g0014 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18983 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18984 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18985 | hp2 | a0015 | c0014 | t0001 | g0013 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0314 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18989 | hp1 | a0004 | c0004 | t0001 | g0184 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18990 | hp1 | a0003 | c0003 | t0002 | g0101 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18993 | hp2 | a0004 | c0004 | t0001 | g0193 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18998 | hp1 | a0002 | c0001 | t0001 | g0320 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18998 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19000 | hp1 | a0004 | c0004 | t0001 | g0197 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19001 | hp2 | a0004 | c0004 | t0001 | g0190 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19002 | hp1 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19002 | hp2 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19003 | hp1 | a0003 | c0003 | t0002 | g0045 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0319 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19004 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19005 | hp1 | a0004 | c0004 | t0001 | g0192 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19005 | hp2 | a0005 | c0005 | t0001 | g0125 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19006 | hp1 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19006 | hp2 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19007 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19009 | hp1 | a0004 | c0004 | t0001 | g0186 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19009 | hp2 | a0001 | c0034 | t0001 | g0247 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0350 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0171 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19030 | hp2 | a0033 | c0024 | t0001 | g0358 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19043 | hp1 | a0005 | c0005 | t0001 | g0156 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19043 | hp2 | a0002 | c0001 | t0001 | g0341 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19055 | hp1 | a0005 | c0005 | t0001 | g0142 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19056 | hp2 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19057 | hp1 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19057 | hp2 | a0004 | c0004 | t0001 | g0195 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19058 | hp1 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19058 | hp2 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19060 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19064 | hp1 | a0005 | c0005 | t0001 | g0120 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19064 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19065 | hp1 | a0004 | c0004 | t0001 | g0178 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19065 | hp2 | a0005 | c0005 | t0001 | g0016 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19067 | hp2 | a0005 | c0005 | t0001 | g0207 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19076 | hp2 | a0002 | c0001 | t0001 | g0326 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19078 | hp2 | a0004 | c0004 | t0001 | g0200 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0351 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19082 | hp1 | a0004 | c0004 | t0001 | g0194 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19084 | hp1 | a0005 | c0005 | t0001 | g0143 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19084 | hp2 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19085 | hp2 | a0005 | c0005 | t0001 | g0137 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0316 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19087 | hp2 | a0003 | c0003 | t0002 | g0109 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19088 | hp1 | a0004 | c0004 | t0001 | g0188 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19088 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19090 | hp1 | a0009 | c0009 | t0001 | g0003 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0332 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19240 | hp1 | a0005 | c0005 | t0001 | g0154 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA19240 | hp2 | a0011 | c0011 | t0001 | g0334 | AFR | YRI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20129 | hp1 | a0005 | c0005 | t0001 | g0155 | AFR | ASW | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0048 | AFR | ASW | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20805 | hp1 | a0034 | c0032 | t0001 | g0118 | EUR | TSI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0020 | EUR | TSI | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20905 | hp1 | a0004 | c0004 | t0001 | g0206 | SAS | GIH | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | GIH | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02109 | hp1 | a0005 | c0005 | t0001 | g0148 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02109 | hp2 | a0002 | c0001 | t0001 | g0312 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02486 | hp2 | a0007 | c0007 | t0002 | g0028 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG02559 | hp2 | a0018 | c0019 | t0001 | g0166 | AFR | ACB | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03471 | hp1 | a0029 | c0020 | t0001 | g0354 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG03471 | hp2 | a0005 | c0005 | t0001 | g0121 | AFR | MSL | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG06807 | hp1 | a0005 | c0005 | t0001 | g0149 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
HG06807 | hp2 | a0006 | c0006 | t0002 | g0042 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18955 | hp1 | a0009 | c0009 | t0001 | g0218 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20300 | hp1 | a0005 | c0005 | t0001 | g0172 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0088 | AFR | USA | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA21309 | hp1 | a0035 | c0028 | t0001 | g0356 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
NA21309 | hp2 | a0036 | c0035 | t0001 | g0213 | AFR | LWK | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0084 | REF | REF | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
homoSapiens | grch38p0 | a0003 | c0003 | t0002 | g0050 | REF | REF | CEP192_chr18_12986362_13130036 | CEP192 | chr18 | 12986362 | 13130036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:13001459 | A | G | 1 | a0027 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.167A>G | p.Tyr56Cys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 247/7960 | 167/7614 | 56/2537 | chr18 | 13001459 | |||
chr18:13001491 | G | A | 1 | a0029 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.199G>A | p.Gly67Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 279/7960 | 199/7614 | 67/2537 | chr18 | 13001491 | |||
chr18:13001513 | G | C | 17 | a0002 a0004 a0006 others(14): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.221G>C | p.Gly74Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 301/7960 | 221/7614 | 74/2537 | chr18 | 13001513 | |||
chr18:13001524 | G | A | 9 | a0002 a0011 a0020 others(6): Show |
83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
missense_variant | MODERATE | c.232G>A | p.Gly78Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/45 | 312/7960 | 232/7614 | 78/2537 | chr18 | 13001524 | |||
chr18:13008498 | G | C | 1 | a0010 | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.333G>C | p.Leu111Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 413/7960 | 333/7614 | 111/2537 | chr18 | 13008498 | |||
chr18:13008578 | C | G | 1 | a0009 | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
missense_variant | MODERATE | c.413C>G | p.Ser138Cys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 493/7960 | 413/7614 | 138/2537 | chr18 | 13008578 | |||
chr18:13015328 | A | C | 2 | a0018 a0028 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
missense_variant&splice_region_variant | MODERATE | c.520A>C | p.Ile174Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/45 | 600/7960 | 520/7614 | 174/2537 | chr18 | 13015328 | |||
chr18:13015367 | A | G | 1 | a0023 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.559A>G | p.Thr187Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/45 | 639/7960 | 559/7614 | 187/2537 | chr18 | 13015367 | |||
chr18:13018510 | T | C | 2 | a0014 a0025 |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.820T>C | p.Phe274Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/45 | 900/7960 | 820/7614 | 274/2537 | chr18 | 13018510 | |||
chr18:13042248 | A | G | 2 | a0015 a0024 |
4 | HG02132.hp1 NA18944.hp1 NA18983.hp1 others(1): Show |
missense_variant | MODERATE | c.1981A>G | p.Ile661Val | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/45 | 2061/7960 | 1981/7614 | 661/2537 | chr18 | 13042248 | |||
chr18:13049151 | A | G | 1 | a0034 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2360A>G | p.Lys787Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 16/45 | 2440/7960 | 2360/7614 | 787/2537 | chr18 | 13049151 | |||
chr18:13049280 | C | T | 1 | a0034 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2489C>T | p.Thr830Ile | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 16/45 | 2569/7960 | 2489/7614 | 830/2537 | chr18 | 13049280 | |||
chr18:13049812 | GAGC | G | 1 | a0007 | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
conservative_inframe_deletion | MODERATE | c.2941_2943delCAG | p.Gln981del | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/45 | 3021/7960 | 2941/7614 | 981/2537 | INFO_REALIGN_3_PRIME | chr18 | 13049812 | ||
chr18:13049816 | A | G | 1 | a0007 | 10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.2942A>G | p.Gln981Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/45 | 3022/7960 | 2942/7614 | 981/2537 | chr18 | 13049816 | |||
chr18:13053032 | C | T | 1 | a0030 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.3131C>T | p.Ser1044Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/45 | 3211/7960 | 3131/7614 | 1044/2537 | chr18 | 13053032 | |||
chr18:13053058 | A | G | 2 | a0011 a0027 |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.3157A>G | p.Thr1053Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/45 | 3237/7960 | 3157/7614 | 1053/2537 | chr18 | 13053058 | |||
chr18:13055916 | A | C | 1 | a0021 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.3326A>C | p.Gln1109Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3406/7960 | 3326/7614 | 1109/2537 | chr18 | 13055916 | |||
chr18:13056066 | C | G | 1 | a0013 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.3476C>G | p.Pro1159Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3556/7960 | 3476/7614 | 1159/2537 | chr18 | 13056066 | |||
chr18:13056231 | A | G | 1 | a0019 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.3641A>G | p.Gln1214Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3721/7960 | 3641/7614 | 1214/2537 | chr18 | 13056231 | |||
chr18:13056362 | G | A | 1 | a0025 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.3772G>A | p.Ala1258Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3852/7960 | 3772/7614 | 1258/2537 | chr18 | 13056362 | |||
chr18:13056561 | G | C | 1 | a0018 | 2 | HG02559.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.3971G>C | p.Gly1324Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4051/7960 | 3971/7614 | 1324/2537 | chr18 | 13056561 | |||
chr18:13056563 | A | C | 1 | a0016 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.3973A>C | p.Thr1325Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4053/7960 | 3973/7614 | 1325/2537 | chr18 | 13056563 | |||
chr18:13056683 | G | A | 3 | a0001 a0022 a0036 |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.4093G>A | p.Val1365Met | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 4173/7960 | 4093/7614 | 1365/2537 | chr18 | 13056683 | |||
chr18:13057656 | C | T | 1 | a0022 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.4180C>T | p.Leu1394Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/45 | 4260/7960 | 4180/7614 | 1394/2537 | chr18 | 13057656 | |||
chr18:13057699 | T | G | 1 | a0024 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.4223T>G | p.Ile1408Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/45 | 4303/7960 | 4223/7614 | 1408/2537 | chr18 | 13057699 | |||
chr18:13059223 | T | C | 1 | a0032 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.4399T>C | p.Cys1467Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4479/7960 | 4399/7614 | 1467/2537 | chr18 | 13059223 | |||
chr18:13068110 | G | A | 2 | a0001 a0022 |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
missense_variant | MODERATE | c.4631G>A | p.Arg1544His | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4711/7960 | 4631/7614 | 1544/2537 | chr18 | 13068110 | |||
chr18:13068133 | T | C | 28 | a0001 a0002 a0004 others(25): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
missense_variant | MODERATE | c.4654T>C | p.Ser1552Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4734/7960 | 4654/7614 | 1552/2537 | chr18 | 13068133 | |||
chr18:13068235 | C | G | 1 | a0019 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant&splice_region_variant | MODERATE | c.4756C>G | p.Gln1586Glu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4836/7960 | 4756/7614 | 1586/2537 | chr18 | 13068235 | |||
chr18:13069132 | A | G | 1 | a0017 | 2 | HG02080.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.5006A>G | p.His1669Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/45 | 5086/7960 | 5006/7614 | 1669/2537 | chr18 | 13069132 | |||
chr18:13069783 | C | T | 29 | a0001 a0002 a0004 others(26): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
missense_variant | MODERATE | c.5101C>T | p.Leu1701Phe | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/45 | 5181/7960 | 5101/7614 | 1701/2537 | chr18 | 13069783 | |||
chr18:13071110 | C | T | 1 | a0020 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.5246C>T | p.Ser1749Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/45 | 5326/7960 | 5246/7614 | 1749/2537 | chr18 | 13071110 | |||
chr18:13087048 | A | G | 1 | a0008 | 8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
missense_variant | MODERATE | c.5648A>G | p.Asn1883Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/45 | 5728/7960 | 5648/7614 | 1883/2537 | chr18 | 13087048 | |||
chr18:13089457 | G | T | 1 | a0035 | 1 | NA21309.hp1 | missense_variant&splice_region_variant | MODERATE | c.5995G>T | p.Ala1999Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/45 | 6075/7960 | 5995/7614 | 1999/2537 | chr18 | 13089457 | |||
chr18:13092425 | G | A | 2 | a0004 a0031 |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
missense_variant | MODERATE | c.6152G>A | p.Ser2051Asn | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/45 | 6232/7960 | 6152/7614 | 2051/2537 | chr18 | 13092425 | |||
chr18:13095592 | G | A | 3 | a0001 a0022 a0036 |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.6344G>A | p.Arg2115Gln | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6424/7960 | 6344/7614 | 2115/2537 | chr18 | 13095592 | |||
chr18:13095610 | T | C | 29 | a0001 a0002 a0004 others(26): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
missense_variant | MODERATE | c.6362T>C | p.Leu2121Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6442/7960 | 6362/7614 | 2121/2537 | chr18 | 13095610 | |||
chr18:13095627 | G | A | 1 | a0031 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.6379G>A | p.Glu2127Lys | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6459/7960 | 6379/7614 | 2127/2537 | chr18 | 13095627 | |||
chr18:13095655 | A | G | 2 | a0014 a0025 |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.6407A>G | p.His2136Arg | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/45 | 6487/7960 | 6407/7614 | 2136/2537 | chr18 | 13095655 | |||
chr18:13100327 | G | A | 1 | a0010 | 7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.6686G>A | p.Arg2229Gln | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/45 | 6766/7960 | 6686/7614 | 2229/2537 | chr18 | 13100327 | |||
chr18:13100452 | A | G | 2 | a0004 a0031 |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
missense_variant | MODERATE | c.6811A>G | p.Lys2271Glu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/45 | 6891/7960 | 6811/7614 | 2271/2537 | chr18 | 13100452 | |||
chr18:13105006 | T | G | 1 | a0026 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6974T>G | p.Val2325Gly | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/45 | 7054/7960 | 6974/7614 | 2325/2537 | chr18 | 13105006 | |||
chr18:13105034 | A | T | 1 | a0033 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.7002A>T | p.Arg2334Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/45 | 7082/7960 | 7002/7614 | 2334/2537 | chr18 | 13105034 | |||
chr18:13116433 | G | T | 30 | a0001 a0002 a0004 others(27): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
missense_variant | MODERATE | c.7346G>T | p.Arg2449Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/45 | 7426/7960 | 7346/7614 | 2449/2537 | chr18 | 13116433 | |||
chr18:13124770 | A | T | 1 | a0001 | 1 | HG03654.hp2 | stop_lost | HIGH | c.7614A>T | p.Ter2538Tyrext*? | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 7694/7960 | 7614/7614 | 2538/2537 | chr18 | 13124770 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:13008564 | C | T | 1 | a0001c0044 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.399C>T | p.Ala133Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/45 | 479/7960 | 399/7614 | 133/2537 | chr18 | 13008564 | |||
chr18:13019206 | T | C | 3 | a0014c0012 a0025c0031 a0034c0032 |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.1050T>C | p.Ser350Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/45 | 1130/7960 | 1050/7614 | 350/2537 | chr18 | 13019206 | |||
chr18:13038432 | A | G | 2 | a0004c0004 a0031c0030 |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
synonymous_variant | LOW | c.1662A>G | p.Thr554Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/45 | 1742/7960 | 1662/7614 | 554/2537 | chr18 | 13038432 | |||
chr18:13040859 | A | G | 2 | a0013c0016 a0013c0029 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1839A>G | p.Pro613Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/45 | 1919/7960 | 1839/7614 | 613/2537 | chr18 | 13040859 | |||
chr18:13055830 | C | T | 1 | a0001c0040 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.3240C>T | p.Ala1080Ala | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3320/7960 | 3240/7614 | 1080/2537 | chr18 | 13055830 | |||
chr18:13056082 | G | C | 1 | a0001c0033 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.3492G>C | p.Pro1164Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3572/7960 | 3492/7614 | 1164/2537 | chr18 | 13056082 | |||
chr18:13056334 | C | T | 10 | a0002c0001 a0002c0022 a0002c0023 others(7): Show |
82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
synonymous_variant | LOW | c.3744C>T | p.His1248His | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/45 | 3824/7960 | 3744/7614 | 1248/2537 | chr18 | 13056334 | |||
chr18:13059096 | A | G | 1 | a0001c0036 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.4272A>G | p.Thr1424Thr | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4352/7960 | 4272/7614 | 1424/2537 | chr18 | 13059096 | |||
chr18:13059174 | A | G | 1 | a0009c0009 | 7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
synonymous_variant | LOW | c.4350A>G | p.Pro1450Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/45 | 4430/7960 | 4350/7614 | 1450/2537 | chr18 | 13059174 | |||
chr18:13067906 | T | C | 2 | a0018c0019 a0028c0043 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.4564T>C | p.Leu1522Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 22/45 | 4644/7960 | 4564/7614 | 1522/2537 | chr18 | 13067906 | |||
chr18:13068192 | C | A | 1 | a0013c0016 | 2 | HG03041.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.4713C>A | p.Gly1571Gly | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/45 | 4793/7960 | 4713/7614 | 1571/2537 | chr18 | 13068192 | |||
chr18:13092480 | C | T | 1 | a0012c0039 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.6207C>T | p.Ser2069Ser | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/45 | 6287/7960 | 6207/7614 | 2069/2537 | chr18 | 13092480 | |||
chr18:13099554 | C | A | 1 | a0002c0022 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.6636C>A | p.Ile2212Ile | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/45 | 6716/7960 | 6636/7614 | 2212/2537 | chr18 | 13099554 | |||
chr18:13113654 | T | A | 1 | a0001c0034 | 1 | NA19009.hp2 | synonymous_variant | LOW | c.7116T>A | p.Pro2372Pro | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/45 | 7196/7960 | 7116/7614 | 2372/2537 | chr18 | 13113654 | |||
chr18:13117641 | G | A | 1 | a0002c0023 | 1 | HG00639.hp1 | splice_region_variant&synonymous_variant | LOW | c.7473G>A | p.Leu2491Leu | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/45 | 7553/7960 | 7473/7614 | 2491/2537 | chr18 | 13117641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:12991377 | C | T | 1 | a0003c0003t0006 | 1 | NA18968.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/45 | 8048 | chr18 | 12991377 | ||||||
chr18:12991394 | T | C | 37 | a0001c0002t0001 a0001c0002t0005 a0001c0033t0001 others(34): Show |
290 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(287): Show |
5_prime_UTR_variant | MODIFIER | c.-48T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/45 | 8031 | chr18 | 12991394 | ||||||
chr18:13124935 | T | C | 1 | a0004c0004t0004 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 165 | chr18 | 13124935 | ||||||
chr18:13125021 | A | G | 2 | a0013c0016t0003 a0013c0029t0003 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 45/45 | 251 | chr18 | 13125021 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:12991522 | C | T | 83 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(80): Show |
87 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+85C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991522 | |||||||
chr18:12991526 | G | A | 9 | a0006c0006t0002g0026 a0007c0007t0002g0006 a0007c0007t0002g0007 others(6): Show |
11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+89G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991526 | |||||||
chr18:12991554 | G | T | 5 | a0007c0007t0002g0006 a0007c0007t0002g0007 a0007c0007t0002g0028 others(2): Show |
7 | HG02486.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+117G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991554 | |||||||
chr18:12991578 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0032 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-5+141G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991578 | |||||||
chr18:12991618 | G | T | 67 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(64): Show |
70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-5+181G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991618 | |||||||
chr18:12991632 | C | A | 2 | a0011c0011t0001g0282 a0011c0011t0001g0283 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-5+195C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991632 | |||||||
chr18:12991845 | T | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+408T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991845 | |||||||
chr18:12991920 | A | ATG | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+483_-5+484insTG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12991920 | |||||||
chr18:12992163 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-5+726C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992163 | |||||||
chr18:12992173 | T | TA | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+737dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12992173 | ||||||
chr18:12992220 | A | T | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-5+783A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992220 | |||||||
chr18:12992262 | C | G | 161 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(158): Show |
171 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-5+825C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992262 | |||||||
chr18:12992276 | A | G | 1 | a0002c0001t0001g0360 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-5+839A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992276 | |||||||
chr18:12992279 | C | A | 2 | a0005c0005t0001g0115 a0005c0005t0001g0116 |
2 | HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-5+842C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992279 | |||||||
chr18:12992308 | C | A | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+871C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992308 | |||||||
chr18:12992314 | G | A | 1 | a0004c0004t0001g0117 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-5+877G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992314 | |||||||
chr18:12992403 | T | C | 1 | a0001c0002t0001g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-5+966T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992403 | |||||||
chr18:12992524 | T | C | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5+1087T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992524 | |||||||
chr18:12992551 | G | T | 1 | a0004c0004t0001g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5+1114G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992551 | |||||||
chr18:12992559 | T | C | 2 | a0002c0001t0001g0020 a0002c0001t0001g0285 |
3 | HG00735.hp1 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-5+1122T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992559 | |||||||
chr18:12992630 | T | C | 1 | a0004c0004t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+1193T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992630 | |||||||
chr18:12992666 | T | C | 1 | a0005c0005t0001g0120 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5+1229T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992666 | |||||||
chr18:12992830 | T | A | 1 | a0001c0002t0001g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+1393T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992830 | |||||||
chr18:12992853 | G | C | 4 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG02132.hp2 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1416G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992853 | |||||||
chr18:12992904 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+1467A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992904 | |||||||
chr18:12992978 | A | G | 2 | a0005c0005t0001g0016 a0005c0005t0001g0207 |
3 | HG02071.hp1 NA19065.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-5+1541A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12992978 | |||||||
chr18:12993158 | G | T | 2 | a0004c0004t0001g0205 a0004c0004t0001g0206 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-5+1721G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993158 | |||||||
chr18:12993196 | A | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+1759A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993196 | |||||||
chr18:12993249 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+1812G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993249 | |||||||
chr18:12993357 | G | A | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-5+1920G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993357 | |||||||
chr18:12993382 | A | G | 1 | a0001c0002t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-5+1945A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993382 | |||||||
chr18:12993544 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+2107A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993544 | |||||||
chr18:12993598 | G | T | 30 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(27): Show |
40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-5+2161G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993598 | |||||||
chr18:12993606 | C | T | 1 | a0005c0005t0001g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-5+2169C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993606 | |||||||
chr18:12993684 | T | G | 1 | a0004c0004t0001g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-5+2247T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993684 | |||||||
chr18:12993710 | C | T | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+2273C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993710 | |||||||
chr18:12993748 | CTCTT | C | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2314_-5+2317del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12993748 | ||||||
chr18:12993760 | C | T | 2 | a0010c0010t0002g0111 a0010c0010t0002g0112 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+2323C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993760 | |||||||
chr18:12993889 | C | T | 1 | a0003c0003t0002g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-5+2452C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993889 | |||||||
chr18:12993902 | C | T | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-5+2465C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12993902 | |||||||
chr18:12994247 | C | T | 1 | a0005c0005t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-5+2810C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994247 | |||||||
chr18:12994251 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-5+2814G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994251 | |||||||
chr18:12994444 | G | A | 1 | a0005c0005t0001g0120 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-5+3007G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994444 | |||||||
chr18:12994469 | G | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+3032G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994469 | |||||||
chr18:12994592 | G | A | 1 | a0002c0001t0001g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-5+3155G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994592 | |||||||
chr18:12994779 | C | T | 85 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(82): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-5+3342C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994779 | |||||||
chr18:12994784 | G | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-5+3347G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994784 | |||||||
chr18:12994852 | G | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+3415G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994852 | |||||||
chr18:12994966 | A | C | 1 | a0003c0003t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-5+3529A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12994966 | |||||||
chr18:12995053 | A | AT | 17 | a0003c0003t0002g0011 a0003c0003t0002g0097 a0003c0003t0002g0098 others(14): Show |
19 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+3642dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | ||||||
chr18:12995053 | ATT | A | 43 | a0001c0002t0001g0019 a0001c0002t0001g0032 a0001c0002t0001g0266 others(40): Show |
44 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5+3641_-5+3642del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | ||||||
chr18:12995053 | ATTT | A | 232 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0031 others(229): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-5+3640_-5+3642del others(3): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | ||||||
chr18:12995053 | ATTTT | A | 13 | a0002c0001t0001g0287 a0002c0001t0001g0288 a0004c0004t0001g0173 others(10): Show |
16 | HG00621.hp2 HG01069.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+3639_-5+3642del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | INFO_REALIGN_3_PRIME | chr18 | 12995053 | ||||||
chr18:12995122 | C | T | 4 | a0002c0001t0001g0345 a0018c0019t0001g0165 a0018c0019t0001g0166 others(1): Show |
4 | HG02040.hp1 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+3685C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995122 | |||||||
chr18:12995130 | C | T | 150 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(147): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-5+3693C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995130 | |||||||
chr18:12995186 | T | C | 287 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(284): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-5+3749T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995186 | |||||||
chr18:12995207 | G | T | 1 | a0002c0001t0001g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-5+3770G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995207 | |||||||
chr18:12995223 | G | A | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-5+3786G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995223 | |||||||
chr18:12995307 | G | A | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+3870G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995307 | |||||||
chr18:12995315 | C | G | 1 | a0001c0002t0001g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+3878C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995315 | |||||||
chr18:12995342 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+3905G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995342 | |||||||
chr18:12995380 | A | T | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-5+3943A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995380 | |||||||
chr18:12995472 | G | A | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-4-3949G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995472 | |||||||
chr18:12995546 | G | A | 57 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(54): Show |
59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.-4-3875G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995546 | |||||||
chr18:12995963 | C | T | 1 | a0005c0005t0001g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4-3458C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12995963 | |||||||
chr18:12996047 | G | A | 1 | a0002c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4-3374G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996047 | |||||||
chr18:12996110 | G | A | 1 | a0006c0006t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-4-3311G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996110 | |||||||
chr18:12996170 | G | A | 2 | a0002c0001t0001g0287 a0002c0001t0001g0289 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4-3251G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996170 | |||||||
chr18:12996262 | A | G | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.-4-3159A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996262 | |||||||
chr18:12996411 | AT | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-3009delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996411 | |||||||
chr18:12996438 | A | C | 1 | a0007c0007t0002g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4-2983A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996438 | |||||||
chr18:12996445 | G | A | 1 | a0002c0001t0001g0290 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-4-2976G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996445 | |||||||
chr18:12996501 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-2920C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996501 | |||||||
chr18:12996535 | C | T | 1 | a0003c0003t0002g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4-2886C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996535 | |||||||
chr18:12996536 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-2885G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996536 | |||||||
chr18:12996572 | C | T | 3 | a0002c0001t0001g0288 a0002c0001t0001g0343 a0023c0027t0001g0342 |
3 | HG00323.hp2 HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-4-2849C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996572 | |||||||
chr18:12996577 | A | T | 1 | a0005c0005t0001g0162 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4-2844A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996577 | |||||||
chr18:12996746 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-4-2675C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12996746 | |||||||
chr18:12997024 | C | G | 1 | a0001c0002t0001g0278 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-4-2397C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997024 | |||||||
chr18:12997144 | G | T | 4 | a0003c0003t0002g0009 a0003c0003t0002g0092 a0003c0003t0002g0093 others(1): Show |
5 | NA18612.hp1 NA19007.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-2277G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997144 | |||||||
chr18:12997288 | A | G | 1 | a0004c0004t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-4-2133A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997288 | |||||||
chr18:12997544 | T | C | 1 | a0002c0023t0001g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4-1877T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997544 | |||||||
chr18:12997645 | A | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1776A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997645 | |||||||
chr18:12997774 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-1647A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997774 | |||||||
chr18:12997795 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4-1626G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12997795 | |||||||
chr18:12998006 | T | G | 1 | a0002c0001t0001g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-4-1415T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998006 | |||||||
chr18:12998268 | G | A | 137 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(134): Show |
142 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-4-1153G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998268 | |||||||
chr18:12998356 | A | C | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-1065A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998356 | |||||||
chr18:12998437 | A | G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-984A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998437 | |||||||
chr18:12998656 | G | A | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-4-765G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998656 | |||||||
chr18:12998930 | G | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-491G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12998930 | |||||||
chr18:12999143 | T | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-278T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 1/44 | chr18 | 12999143 | |||||||
chr18:12999620 | G | C | 1 | a0005c0005t0001g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.164+32G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999620 | |||||||
chr18:12999676 | G | A | 1 | a0003c0003t0002g0044 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.164+88G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999676 | |||||||
chr18:12999755 | C | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+167C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999755 | |||||||
chr18:12999822 | C | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+234C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999822 | |||||||
chr18:12999828 | A | AT | 11 | a0002c0001t0001g0332 a0002c0001t0001g0352 a0003c0003t0002g0090 others(8): Show |
11 | HG01099.hp1 HG01515.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.164+258dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | ||||||
chr18:12999828 | AT | A | 63 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(60): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.164+258delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | ||||||
chr18:12999828 | ATTTTTTT | A | 61 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(58): Show |
63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.164+252_164+258del others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 12999828 | ||||||
chr18:12999965 | A | G | 231 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(228): Show |
253 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.164+377A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999965 | |||||||
chr18:12999987 | G | A | 4 | a0003c0003t0002g0009 a0003c0003t0002g0092 a0003c0003t0002g0093 others(1): Show |
5 | NA18612.hp1 NA19007.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+399G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 12999987 | |||||||
chr18:13000085 | T | TTCTCTC | 12 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(9): Show |
14 | HG01952.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.164+499_164+504dup others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000085 | ||||||
chr18:13000091 | C | CT | 35 | a0003c0003t0002g0085 a0003c0003t0002g0095 a0003c0003t0002g0105 others(32): Show |
45 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.164+530dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT | 27 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(24): Show |
30 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT others(1): Show |
13 | a0002c0001t0001g0289 a0002c0001t0001g0290 a0002c0001t0001g0305 others(10): Show |
13 | HG00438.hp2 HG01361.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT others(2): Show |
9 | a0002c0001t0001g0314 a0002c0001t0001g0315 a0002c0001t0001g0316 others(6): Show |
9 | HG02040.hp1 HG02976.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT others(3): Show |
13 | a0002c0001t0001g0023 a0002c0001t0001g0317 a0002c0001t0001g0318 others(10): Show |
14 | HG00673.hp1 HG01099.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT others(4): Show |
6 | a0002c0001t0001g0325 a0002c0001t0001g0326 a0002c0001t0001g0327 others(3): Show |
6 | HG02523.hp2 HG03516.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTCTCTTT others(5): Show |
3 | a0002c0001t0001g0328 a0002c0001t0001g0329 a0002c0001t0001g0330 |
3 | HG00423.hp2 NA18954.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.164+504_164+505ins others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | C | CTT | 10 | a0003c0003t0002g0086 a0003c0003t0002g0087 a0003c0003t0002g0088 others(7): Show |
10 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.164+529_164+530dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CT | C | 11 | a0001c0002t0001g0211 a0001c0002t0001g0223 a0001c0002t0001g0224 others(8): Show |
11 | HG02004.hp2 HG02132.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.164+530delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CTTTT | C | 6 | a0002c0001t0001g0293 a0002c0001t0001g0336 a0002c0001t0001g0337 others(3): Show |
6 | HG00741.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+527_164+530del others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CTTTTTT | C | 6 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(3): Show |
6 | HG01109.hp2 HG01981.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+525_164+530del others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CTTTTTTT | C | 9 | a0001c0036t0001g0222 a0005c0005t0001g0124 a0009c0009t0001g0003 others(6): Show |
12 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+524_164+530del others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CTTTTTTT others(1): Show |
C | 58 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(55): Show |
60 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.164+523_164+530del others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000091 | CTTTTTTT others(3): Show |
C | 1 | a0005c0005t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164+521_164+530del others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000091 | ||||||
chr18:13000092 | T | TC | 4 | a0001c0002t0001g0230 a0001c0002t0001g0258 a0001c0002t0001g0272 others(1): Show |
4 | HG02559.hp1 HG03654.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+504_164+505ins others(1): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000092 | |||||||
chr18:13000093 | T | C | 63 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(60): Show |
66 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.164+505T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000093 | |||||||
chr18:13000094 | T | C | 12 | a0001c0002t0001g0211 a0001c0002t0001g0223 a0001c0002t0001g0224 others(9): Show |
12 | HG02132.hp2 HG02559.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+506T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000094 | |||||||
chr18:13000095 | T | C | 62 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(59): Show |
65 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.164+507T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000095 | |||||||
chr18:13000096 | T | C | 11 | a0001c0002t0001g0211 a0001c0002t0001g0223 a0001c0002t0001g0224 others(8): Show |
11 | HG01515.hp1 HG02132.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.164+508T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000096 | |||||||
chr18:13000097 | T | C | 6 | a0002c0001t0001g0293 a0002c0001t0001g0336 a0002c0001t0001g0337 others(3): Show |
6 | HG00741.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+509T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000097 | |||||||
chr18:13000098 | T | C | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.164+510T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000098 | |||||||
chr18:13000099 | T | C | 7 | a0002c0001t0001g0293 a0002c0001t0001g0336 a0002c0001t0001g0337 others(4): Show |
7 | HG00741.hp1 HG01109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+511T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000099 | |||||||
chr18:13000100 | T | C | 9 | a0001c0036t0001g0222 a0005c0005t0001g0124 a0009c0009t0001g0003 others(6): Show |
12 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+512T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000100 | |||||||
chr18:13000101 | T | C | 59 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(56): Show |
61 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+513T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000101 | |||||||
chr18:13000102 | T | C | 10 | a0001c0036t0001g0222 a0005c0005t0001g0124 a0005c0005t0001g0161 others(7): Show |
13 | HG00621.hp2 HG01167.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.164+514T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000102 | |||||||
chr18:13000103 | T | C | 59 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(56): Show |
61 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+515T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000103 | |||||||
chr18:13000104 | T | C | 1 | a0005c0005t0001g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.164+516T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000104 | |||||||
chr18:13000167 | A | G | 85 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.164+579A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000167 | |||||||
chr18:13000211 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.164+623A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000211 | |||||||
chr18:13000231 | TAC | T | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.164+647_164+648del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr18 | 13000231 | ||||||
chr18:13000278 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.164+690A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000278 | |||||||
chr18:13000339 | C | T | 2 | a0012c0013t0002g0083 a0012c0039t0002g0104 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.164+751C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000339 | |||||||
chr18:13000438 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+850A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000438 | |||||||
chr18:13000486 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.164+898G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000486 | |||||||
chr18:13000547 | A | G | 40 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(37): Show |
42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.165-910A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000547 | |||||||
chr18:13000548 | T | C | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-909T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000548 | |||||||
chr18:13000737 | C | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.165-720C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000737 | |||||||
chr18:13000976 | C | T | 150 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(147): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.165-481C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13000976 | |||||||
chr18:13001343 | C | T | 2 | a0003c0003t0002g0081 a0003c0003t0002g0082 |
2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.165-114C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001343 | |||||||
chr18:13001380 | C | T | 1 | a0002c0001t0001g0313 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.165-77C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001380 | |||||||
chr18:13001411 | T | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-46T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 2/44 | chr18 | 13001411 | |||||||
chr18:13001705 | T | C | 61 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(58): Show |
63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.290+123T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13001705 | |||||||
chr18:13001949 | C | A | 79 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(76): Show |
83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.290+367C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13001949 | |||||||
chr18:13002010 | G | A | 1 | a0001c0002t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.290+428G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002010 | |||||||
chr18:13002197 | C | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.290+615C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002197 | |||||||
chr18:13002304 | G | C | 1 | a0005c0005t0001g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.290+722G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002304 | |||||||
chr18:13002309 | AGC | A | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+728_290+729del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002309 | |||||||
chr18:13002310 | G | A | 150 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(147): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.290+728G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002310 | |||||||
chr18:13002312 | T | A | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+730T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002312 | |||||||
chr18:13002353 | C | G | 67 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(64): Show |
69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.290+771C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002353 | |||||||
chr18:13002497 | G | T | 7 | a0010c0010t0002g0047 a0010c0010t0002g0078 a0010c0010t0002g0079 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+915G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002497 | |||||||
chr18:13002755 | G | T | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+1173G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002755 | |||||||
chr18:13002798 | TGTATTTG others(1): Show |
T | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.290+1223_290+1230d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13002798 | ||||||
chr18:13002807 | G | A | 1 | a0012c0013t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.290+1225G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13002807 | |||||||
chr18:13003192 | T | A | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+1610T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003192 | |||||||
chr18:13003225 | G | C | 89 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.290+1643G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003225 | |||||||
chr18:13003268 | G | A | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.290+1686G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003268 | |||||||
chr18:13003391 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.290+1809A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003391 | |||||||
chr18:13003436 | G | A | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.290+1854G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003436 | |||||||
chr18:13003451 | GA | G | 136 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(133): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.290+1890delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | ||||||
chr18:13003451 | GAA | G | 9 | a0002c0001t0001g0287 a0002c0001t0001g0290 a0002c0001t0001g0304 others(6): Show |
9 | HG01167.hp2 HG01256.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1889_290+1890d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | ||||||
chr18:13003451 | GAAAAA | G | 135 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(132): Show |
140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.290+1886_290+1890d others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003451 | ||||||
chr18:13003480 | T | C | 1 | a0013c0029t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290+1898T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003480 | |||||||
chr18:13003548 | T | A | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+1966T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003548 | |||||||
chr18:13003579 | A | T | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+1997A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003579 | |||||||
chr18:13003605 | C | A | 1 | a0005c0005t0001g0125 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.290+2023C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003605 | |||||||
chr18:13003630 | A | G | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+2048A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003630 | |||||||
chr18:13003873 | TTGTC | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+2294_290+2297d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13003873 | ||||||
chr18:13003912 | G | T | 1 | a0004c0004t0001g0197 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.290+2330G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13003912 | |||||||
chr18:13004062 | A | C | 2 | a0005c0005t0001g0148 a0005c0005t0001g0149 |
2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.290+2480A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004062 | |||||||
chr18:13004105 | T | G | 9 | a0006c0006t0002g0026 a0007c0007t0002g0006 a0007c0007t0002g0007 others(6): Show |
11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+2523T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004105 | |||||||
chr18:13004193 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.290+2611G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004193 | |||||||
chr18:13004201 | T | C | 1 | a0017c0017t0002g0010 | 2 | HG02080.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.290+2619T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004201 | |||||||
chr18:13004252 | C | T | 61 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(58): Show |
63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.290+2670C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004252 | |||||||
chr18:13004260 | T | C | 1 | a0001c0002t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.290+2678T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004260 | |||||||
chr18:13004273 | G | T | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+2691G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004273 | |||||||
chr18:13004299 | C | CT | 139 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(136): Show |
144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.290+2728dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13004299 | ||||||
chr18:13004421 | C | T | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.290+2839C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004421 | |||||||
chr18:13004453 | C | T | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+2871C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004453 | |||||||
chr18:13004732 | A | G | 44 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(41): Show |
46 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.290+3150A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004732 | |||||||
chr18:13004826 | G | A | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+3244G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004826 | |||||||
chr18:13004998 | C | T | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+3416C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004998 | |||||||
chr18:13004999 | A | C | 1 | a0002c0001t0001g0303 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.290+3417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13004999 | |||||||
chr18:13005474 | T | C | 290 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(287): Show |
314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.291-2982T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005474 | |||||||
chr18:13005541 | C | G | 1 | a0005c0005t0001g0170 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.291-2915C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005541 | |||||||
chr18:13005629 | G | C | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.291-2827G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005629 | |||||||
chr18:13005668 | C | A | 4 | a0002c0001t0001g0340 a0002c0001t0001g0341 a0002c0001t0001g0359 others(1): Show |
4 | HG02976.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-2788C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005668 | |||||||
chr18:13005917 | G | A | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.291-2539G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005917 | |||||||
chr18:13005950 | A | G | 1 | a0031c0030t0001g0175 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.291-2506A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13005950 | |||||||
chr18:13006113 | C | T | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-2343C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006113 | |||||||
chr18:13006196 | A | G | 1 | a0001c0002t0001g0211 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.291-2260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006196 | |||||||
chr18:13006285 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-2171A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006285 | |||||||
chr18:13006327 | C | T | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2129C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006327 | |||||||
chr18:13006404 | A | G | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2052A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006404 | |||||||
chr18:13006598 | A | G | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.291-1858A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006598 | |||||||
chr18:13006765 | TG | T | 61 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(58): Show |
63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.291-1690delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13006765 | |||||||
chr18:13007154 | T | C | 1 | a0026c0038t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291-1302T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007154 | |||||||
chr18:13007195 | A | G | 1 | a0004c0004t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.291-1261A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007195 | |||||||
chr18:13007339 | A | G | 2 | a0003c0003t0002g0076 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.291-1117A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007339 | |||||||
chr18:13007347 | C | A | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.291-1109C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007347 | |||||||
chr18:13007481 | T | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.291-975T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007481 | |||||||
chr18:13007516 | G | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.291-940G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007516 | |||||||
chr18:13007558 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.291-898C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007558 | |||||||
chr18:13007621 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.291-835A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007621 | |||||||
chr18:13007828 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.291-628C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007828 | |||||||
chr18:13007830 | C | T | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-626C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13007830 | |||||||
chr18:13008124 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-332G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008124 | |||||||
chr18:13008246 | C | CTG | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.291-208_291-207dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | INFO_REALIGN_3_PRIME | chr18 | 13008246 | ||||||
chr18:13008308 | T | C | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291-148T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008308 | |||||||
chr18:13008309 | A | G | 1 | a0005c0005t0001g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.291-147A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008309 | |||||||
chr18:13008370 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.291-86A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008370 | |||||||
chr18:13008377 | A | G | 1 | a0003c0003t0002g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.291-79A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008377 | |||||||
chr18:13008393 | T | C | 1 | a0001c0002t0001g0265 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.291-63T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 3/44 | chr18 | 13008393 | |||||||
chr18:13008702 | A | AT | 23 | a0001c0002t0001g0019 a0001c0002t0001g0264 a0001c0002t0001g0266 others(20): Show |
24 | HG00438.hp2 HG01192.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.466+89dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13008702 | ||||||
chr18:13008742 | C | T | 22 | a0003c0003t0002g0009 a0003c0003t0002g0045 a0003c0003t0002g0046 others(19): Show |
23 | HG00558.hp1 HG00597.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.466+111C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008742 | |||||||
chr18:13008895 | A | G | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+264A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008895 | |||||||
chr18:13008969 | A | G | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466+338A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13008969 | |||||||
chr18:13009008 | C | CT | 11 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0259 others(8): Show |
11 | HG02293.hp1 HG02451.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+382dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009008 | ||||||
chr18:13009012 | TTG | T | 53 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0116 others(50): Show |
55 | HG00099.hp2 HG01071.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.466+383_466+384del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009012 | ||||||
chr18:13009013 | TG | T | 11 | a0005c0005t0001g0115 a0005c0005t0001g0121 a0005c0005t0001g0122 others(8): Show |
11 | HG01167.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+383delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009013 | |||||||
chr18:13009014 | G | GT | 8 | a0003c0003t0002g0090 a0003c0003t0002g0094 a0003c0003t0002g0107 others(5): Show |
8 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+400dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | ||||||
chr18:13009014 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.466+383G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009014 | |||||||
chr18:13009014 | GT | G | 42 | a0002c0001t0001g0350 a0003c0003t0002g0089 a0004c0004t0001g0001 others(39): Show |
52 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.466+400delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | ||||||
chr18:13009014 | GTT | G | 104 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(101): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.466+399_466+400del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13009014 | ||||||
chr18:13009289 | G | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+658G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009289 | |||||||
chr18:13009366 | T | C | 4 | a0001c0002t0001g0017 a0001c0002t0001g0229 a0001c0002t0001g0231 others(1): Show |
5 | HG02523.hp1 NA18940.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+735T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009366 | |||||||
chr18:13009409 | C | T | 61 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(58): Show |
63 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.466+778C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009409 | |||||||
chr18:13009443 | T | A | 1 | a0002c0001t0001g0317 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.466+812T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009443 | |||||||
chr18:13009447 | A | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.466+816A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009447 | |||||||
chr18:13009482 | G | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466+851G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009482 | |||||||
chr18:13009597 | C | G | 1 | a0002c0001t0001g0348 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.466+966C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009597 | |||||||
chr18:13009623 | A | G | 3 | a0011c0011t0001g0335 a0011c0011t0001g0353 a0027c0045t0001g0333 |
3 | HG02723.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.466+992A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009623 | |||||||
chr18:13009731 | G | C | 57 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(54): Show |
59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.466+1100G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009731 | |||||||
chr18:13009906 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.466+1275T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009906 | |||||||
chr18:13009913 | G | A | 1 | a0005c0005t0001g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.466+1282G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13009913 | |||||||
chr18:13010017 | G | A | 85 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(82): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+1386G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010017 | |||||||
chr18:13010128 | C | A | 1 | a0001c0002t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.466+1497C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010128 | |||||||
chr18:13010182 | T | A | 2 | a0003c0003t0002g0049 a0030c0041t0002g0106 |
2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.466+1551T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010182 | |||||||
chr18:13010191 | C | A | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+1560C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010191 | |||||||
chr18:13010239 | C | G | 150 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(147): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.466+1608C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010239 | |||||||
chr18:13010617 | C | T | 67 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(64): Show |
69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.466+1986C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010617 | |||||||
chr18:13010634 | T | G | 138 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(135): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.466+2003T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010634 | |||||||
chr18:13010702 | C | T | 1 | a0007c0007t0002g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.466+2071C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010702 | |||||||
chr18:13010801 | G | A | 1 | a0005c0005t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.466+2170G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010801 | |||||||
chr18:13010993 | G | A | 1 | a0005c0005t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.467-1980G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13010993 | |||||||
chr18:13011001 | C | T | 57 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(54): Show |
59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.467-1972C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011001 | |||||||
chr18:13011079 | T | C | 2 | a0006c0006t0002g0033 a0006c0006t0002g0036 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.467-1894T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011079 | |||||||
chr18:13011183 | T | C | 287 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(284): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.467-1790T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011183 | |||||||
chr18:13011184 | G | A | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1789G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011184 | |||||||
chr18:13011226 | C | CA | 68 | a0003c0003t0002g0089 a0003c0003t0002g0105 a0005c0005t0001g0014 others(65): Show |
70 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.467-1733dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011226 | ||||||
chr18:13011226 | CA | C | 220 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(217): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.467-1733delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011226 | ||||||
chr18:13011432 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.467-1541T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011432 | |||||||
chr18:13011531 | GT | G | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.467-1433delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chr18 | 13011531 | ||||||
chr18:13011639 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.467-1334C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011639 | |||||||
chr18:13011846 | A | G | 10 | a0001c0002t0001g0251 a0001c0002t0001g0252 a0001c0002t0001g0253 others(7): Show |
10 | HG00673.hp2 HG02040.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1127A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011846 | |||||||
chr18:13011863 | C | G | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-1110C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011863 | |||||||
chr18:13011898 | A | C | 1 | a0003c0003t0002g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.467-1075A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13011898 | |||||||
chr18:13012045 | A | G | 7 | a0010c0010t0002g0047 a0010c0010t0002g0078 a0010c0010t0002g0079 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-928A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012045 | |||||||
chr18:13012153 | C | G | 1 | a0011c0011t0001g0353 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.467-820C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012153 | |||||||
chr18:13012295 | T | A | 150 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(147): Show |
169 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.467-678T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012295 | |||||||
chr18:13012364 | A | G | 1 | a0004c0004t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.467-609A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012364 | |||||||
chr18:13012471 | C | T | 1 | a0002c0001t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.467-502C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012471 | |||||||
chr18:13012483 | C | T | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.467-490C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012483 | |||||||
chr18:13012548 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-425G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012548 | |||||||
chr18:13012651 | T | C | 62 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(59): Show |
64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.467-322T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012651 | |||||||
chr18:13012873 | A | T | 1 | a0008c0008t0001g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.467-100A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 4/44 | chr18 | 13012873 | |||||||
chr18:13013153 | T | C | 2 | a0001c0002t0001g0260 a0001c0002t0001g0267 |
2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.519+128T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013153 | |||||||
chr18:13013196 | G | T | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+171G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013196 | |||||||
chr18:13013203 | GGGTAGTG others(9): Show |
G | 13 | a0006c0006t0002g0026 a0006c0006t0002g0034 a0006c0006t0002g0035 others(10): Show |
15 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.519+181_519+196del others(16): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13013203 | ||||||
chr18:13013231 | C | G | 1 | a0031c0030t0001g0175 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.519+206C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013231 | |||||||
chr18:13013242 | TGATGTCA others(3): Show |
T | 1 | a0010c0010t0002g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.519+218_519+227del others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013242 | |||||||
chr18:13013275 | C | T | 1 | a0010c0010t0002g0103 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.519+250C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013275 | |||||||
chr18:13013310 | T | A | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+285T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013310 | |||||||
chr18:13013391 | C | T | 1 | a0003c0003t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.519+366C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013391 | |||||||
chr18:13013558 | A | G | 1 | a0031c0030t0001g0175 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.519+533A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013558 | |||||||
chr18:13013661 | C | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519+636C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013661 | |||||||
chr18:13013763 | A | C | 2 | a0006c0006t0002g0042 a0006c0006t0002g0043 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.519+738A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13013763 | |||||||
chr18:13014138 | T | C | 4 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(1): Show |
4 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1113T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014138 | |||||||
chr18:13014384 | T | TCTCAC | 6 | a0001c0002t0001g0017 a0001c0002t0001g0229 a0001c0002t0001g0231 others(3): Show |
7 | HG00544.hp2 HG02523.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-940_520-939ins others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13014384 | ||||||
chr18:13014528 | A | G | 6 | a0002c0001t0001g0298 a0002c0001t0001g0299 a0002c0001t0001g0300 others(3): Show |
6 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-800A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014528 | |||||||
chr18:13014792 | C | CATATATA others(4): Show |
3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-526_520-516dup others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr18 | 13014792 | ||||||
chr18:13014864 | G | A | 1 | a0002c0001t0001g0314 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.520-464G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014864 | |||||||
chr18:13014874 | A | G | 1 | a0002c0001t0001g0323 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.520-454A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014874 | |||||||
chr18:13014882 | G | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.520-446G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014882 | |||||||
chr18:13014882 | G | C | 85 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(82): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.520-446G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014882 | |||||||
chr18:13014904 | C | T | 1 | a0002c0023t0001g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.520-424C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014904 | |||||||
chr18:13014927 | T | G | 1 | a0001c0002t0001g0264 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.520-401T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13014927 | |||||||
chr18:13015028 | G | A | 1 | a0001c0002t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.520-300G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015028 | |||||||
chr18:13015147 | G | A | 1 | a0003c0003t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.520-181G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015147 | |||||||
chr18:13015247 | T | C | 67 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(64): Show |
69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.520-81T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015247 | |||||||
chr18:13015292 | A | G | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-36A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 5/44 | chr18 | 13015292 | |||||||
chr18:13015491 | A | C | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.640+43A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015491 | |||||||
chr18:13015510 | T | G | 1 | a0001c0002t0001g0236 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.640+62T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015510 | |||||||
chr18:13015626 | A | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.640+178A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015626 | |||||||
chr18:13015814 | C | T | 4 | a0001c0002t0001g0250 a0013c0016t0003g0215 a0013c0016t0003g0216 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+366C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015814 | |||||||
chr18:13015843 | T | C | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+395T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015843 | |||||||
chr18:13015859 | C | T | 71 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(68): Show |
74 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.640+411C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13015859 | |||||||
chr18:13016036 | G | A | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.640+588G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016036 | |||||||
chr18:13016274 | C | T | 1 | a0002c0001t0001g0303 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.640+826C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016274 | |||||||
chr18:13016475 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.641-713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016475 | |||||||
chr18:13016514 | T | C | 1 | a0005c0005t0001g0126 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.641-674T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016514 | |||||||
chr18:13016737 | C | G | 1 | a0009c0009t0001g0217 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.641-451C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016737 | |||||||
chr18:13016813 | T | C | 1 | a0002c0001t0001g0349 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.641-375T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016813 | |||||||
chr18:13016863 | A | G | 1 | a0005c0005t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.641-325A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13016863 | |||||||
chr18:13017123 | A | G | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG00544.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.641-65A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 6/44 | chr18 | 13017123 | |||||||
chr18:13017416 | T | C | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.789+80T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017416 | |||||||
chr18:13017463 | G | A | 70 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(67): Show |
73 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.789+127G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017463 | |||||||
chr18:13017673 | A | G | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.789+337A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017673 | |||||||
chr18:13017724 | T | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.789+388T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017724 | |||||||
chr18:13017857 | A | G | 1 | a0001c0002t0001g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.789+521A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017857 | |||||||
chr18:13017888 | T | C | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+552T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13017888 | |||||||
chr18:13018072 | A | G | 291 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(288): Show |
315 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.790-408A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018072 | |||||||
chr18:13018080 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-400A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018080 | |||||||
chr18:13018430 | A | G | 1 | a0001c0002t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.790-50A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018430 | |||||||
chr18:13018460 | C | T | 1 | a0004c0004t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.790-20C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 7/44 | chr18 | 13018460 | |||||||
chr18:13018667 | CT | C | 56 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0031 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.925+59delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | INFO_REALIGN_3_PRIME | chr18 | 13018667 | ||||||
chr18:13018674 | T | A | 7 | a0001c0002t0001g0230 a0001c0002t0001g0251 a0001c0002t0001g0252 others(4): Show |
7 | HG02080.hp2 HG02083.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+59T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018674 | |||||||
chr18:13018674 | TA | T | 7 | a0001c0002t0001g0018 a0001c0002t0001g0220 a0001c0002t0001g0233 others(4): Show |
8 | HG02015.hp2 HG02129.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+69delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | INFO_REALIGN_3_PRIME | chr18 | 13018674 | ||||||
chr18:13018675 | A | T | 5 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(2): Show |
5 | HG01891.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+60A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018675 | |||||||
chr18:13018807 | G | A | 1 | a0005c0005t0001g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.925+192G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018807 | |||||||
chr18:13018808 | T | C | 1 | a0036c0035t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.925+193T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018808 | |||||||
chr18:13018966 | A | G | 2 | a0003c0003t0002g0081 a0003c0003t0002g0082 |
2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.926-116A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 8/44 | chr18 | 13018966 | |||||||
chr18:13019264 | G | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+58G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019264 | |||||||
chr18:13019337 | T | C | 89 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+131T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019337 | |||||||
chr18:13019494 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1050+288G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019494 | |||||||
chr18:13019697 | A | G | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1050+491A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019697 | |||||||
chr18:13019873 | C | T | 89 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+667C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019873 | |||||||
chr18:13019893 | A | G | 1 | a0002c0001t0001g0311 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1050+687A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019893 | |||||||
chr18:13019951 | T | G | 4 | a0001c0002t0001g0209 a0001c0002t0001g0212 a0006c0006t0002g0034 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050+745T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13019951 | |||||||
chr18:13020102 | C | T | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1050+896C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020102 | |||||||
chr18:13020167 | T | G | 89 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(86): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1050+961T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020167 | |||||||
chr18:13020250 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1050+1044A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020250 | |||||||
chr18:13020312 | T | C | 2 | a0006c0006t0002g0042 a0006c0006t0002g0043 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+1106T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020312 | |||||||
chr18:13020651 | A | G | 1 | a0001c0002t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1050+1445A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020651 | |||||||
chr18:13020882 | T | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1050+1676T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13020882 | |||||||
chr18:13021020 | T | C | 6 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+1814T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021020 | |||||||
chr18:13021078 | G | T | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1050+1872G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021078 | |||||||
chr18:13021211 | A | G | 1 | a0002c0001t0001g0022 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1050+2005A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021211 | |||||||
chr18:13021274 | G | A | 8 | a0007c0007t0002g0006 a0007c0007t0002g0007 a0007c0007t0002g0024 others(5): Show |
10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050+2068G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021274 | |||||||
chr18:13021305 | G | A | 11 | a0005c0005t0001g0133 a0005c0005t0001g0148 a0005c0005t0001g0149 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1050+2099G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021305 | |||||||
chr18:13021631 | G | A | 243 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1050+2425G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021631 | |||||||
chr18:13021992 | T | C | 1 | a0006c0006t0002g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1050+2786T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13021992 | |||||||
chr18:13022432 | G | C | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1050+3226G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022432 | |||||||
chr18:13022484 | G | A | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1050+3278G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022484 | |||||||
chr18:13022593 | C | T | 3 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 |
3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1050+3387C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022593 | |||||||
chr18:13022607 | C | A | 1 | a0004c0004t0001g0186 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1050+3401C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13022607 | |||||||
chr18:13023026 | A | G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1050+3820A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023026 | |||||||
chr18:13023104 | C | T | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+3898C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023104 | |||||||
chr18:13023150 | A | G | 62 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(59): Show |
64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.1050+3944A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023150 | |||||||
chr18:13023266 | A | G | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1050+4060A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023266 | |||||||
chr18:13023476 | A | AT | 7 | a0001c0002t0001g0227 a0001c0002t0001g0258 a0009c0009t0001g0003 others(4): Show |
10 | HG00621.hp2 HG01928.hp2 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.1050+4284dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13023476 | ||||||
chr18:13023476 | AT | A | 63 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(60): Show |
67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1050+4284delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13023476 | ||||||
chr18:13023569 | A | T | 2 | a0001c0002t0001g0261 a0001c0002t0001g0262 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1050+4363A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023569 | |||||||
chr18:13023761 | C | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1050+4555C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023761 | |||||||
chr18:13023974 | T | C | 1 | a0013c0029t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1050+4768T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13023974 | |||||||
chr18:13024187 | G | A | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+4981G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024187 | |||||||
chr18:13024236 | T | C | 1 | a0015c0014t0001g0013 | 2 | NA18944.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1050+5030T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024236 | |||||||
chr18:13024372 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050+5166A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024372 | |||||||
chr18:13024459 | GTTTA | G | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-5188_1051-518 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13024459 | ||||||
chr18:13024562 | A | G | 2 | a0004c0004t0001g0002 a0004c0004t0001g0195 |
5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-5101A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024562 | |||||||
chr18:13024596 | A | G | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051-5067A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024596 | |||||||
chr18:13024767 | T | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1051-4896T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024767 | |||||||
chr18:13024780 | A | AT | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051-4876dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13024780 | ||||||
chr18:13024793 | C | T | 79 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(76): Show |
83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1051-4870C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024793 | |||||||
chr18:13024848 | C | T | 3 | a0004c0004t0001g0005 a0004c0004t0001g0200 a0004c0004t0001g0202 |
5 | NA18961.hp1 NA18980.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-4815C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024848 | |||||||
chr18:13024849 | G | A | 1 | a0001c0002t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1051-4814G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024849 | |||||||
chr18:13024918 | C | T | 20 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(17): Show |
20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4745C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024918 | |||||||
chr18:13024921 | C | T | 20 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(17): Show |
20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4742C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024921 | |||||||
chr18:13024926 | C | A | 85 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(82): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1051-4737C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13024926 | |||||||
chr18:13025051 | C | T | 20 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(17): Show |
20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-4612C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025051 | |||||||
chr18:13025065 | C | A | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1051-4598C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025065 | |||||||
chr18:13025118 | A | G | 1 | a0008c0008t0001g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1051-4545A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025118 | |||||||
chr18:13025417 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-4246A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025417 | |||||||
chr18:13025672 | C | T | 349 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(346): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1051-3991C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13025672 | |||||||
chr18:13026037 | A | G | 2 | a0005c0005t0001g0143 a0005c0005t0001g0144 |
2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1051-3626A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026037 | |||||||
chr18:13026051 | G | A | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-3612G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026051 | |||||||
chr18:13026055 | A | G | 1 | a0005c0005t0001g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1051-3608A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026055 | |||||||
chr18:13026070 | T | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1051-3593T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026070 | |||||||
chr18:13026106 | T | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-3557T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026106 | |||||||
chr18:13026121 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1051-3542T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026121 | |||||||
chr18:13026367 | G | T | 3 | a0003c0003t0002g0063 a0003c0003t0002g0064 a0017c0017t0002g0010 |
4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-3296G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026367 | |||||||
chr18:13026383 | G | T | 2 | a0001c0002t0001g0211 a0001c0033t0001g0210 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1051-3280G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026383 | |||||||
chr18:13026408 | C | G | 1 | a0002c0001t0001g0313 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1051-3255C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026408 | |||||||
chr18:13026587 | T | A | 1 | a0001c0002t0001g0223 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1051-3076T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026587 | |||||||
chr18:13026604 | G | C | 1 | a0001c0002t0001g0267 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1051-3059G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026604 | |||||||
chr18:13026796 | G | C | 1 | a0012c0013t0002g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1051-2867G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026796 | |||||||
chr18:13026917 | G | GT | 5 | a0001c0002t0001g0258 a0001c0033t0001g0210 a0003c0003t0002g0090 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-2738dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13026917 | ||||||
chr18:13026939 | C | A | 1 | a0008c0008t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1051-2724C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13026939 | |||||||
chr18:13027085 | G | A | 1 | a0011c0011t0001g0334 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1051-2578G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027085 | |||||||
chr18:13027223 | T | C | 3 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 |
3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1051-2440T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027223 | |||||||
chr18:13027542 | G | T | 79 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(76): Show |
83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1051-2121G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027542 | |||||||
chr18:13027555 | C | T | 13 | a0006c0006t0002g0026 a0006c0006t0002g0034 a0006c0006t0002g0035 others(10): Show |
15 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1051-2108C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027555 | |||||||
chr18:13027656 | G | A | 2 | a0002c0001t0001g0287 a0002c0001t0001g0289 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1051-2007G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027656 | |||||||
chr18:13027663 | T | C | 62 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(59): Show |
64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.1051-2000T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027663 | |||||||
chr18:13027800 | G | A | 1 | a0004c0004t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1051-1863G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027800 | |||||||
chr18:13027906 | T | C | 1 | a0026c0038t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-1757T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13027906 | |||||||
chr18:13028102 | C | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1051-1561C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028102 | |||||||
chr18:13028204 | T | G | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-1459T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028204 | |||||||
chr18:13028369 | T | C | 1 | a0030c0041t0002g0106 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1051-1294T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028369 | |||||||
chr18:13028597 | G | A | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051-1066G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028597 | |||||||
chr18:13028634 | CT | C | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1051-1028delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028634 | |||||||
chr18:13028644 | C | G | 1 | a0004c0004t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1051-1019C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028644 | |||||||
chr18:13028645 | G | A | 91 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(88): Show |
96 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1051-1018G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028645 | |||||||
chr18:13028676 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1051-987C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028676 | |||||||
chr18:13028767 | G | A | 1 | a0004c0004t0004g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1051-896G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028767 | |||||||
chr18:13028966 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1051-697G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13028966 | |||||||
chr18:13029069 | T | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1051-594T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029069 | |||||||
chr18:13029118 | G | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-545G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029118 | |||||||
chr18:13029148 | G | GT | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051-511dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | INFO_REALIGN_3_PRIME | chr18 | 13029148 | ||||||
chr18:13029158 | G | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1051-505G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029158 | |||||||
chr18:13029201 | A | C | 1 | a0002c0001t0001g0332 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051-462A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029201 | |||||||
chr18:13029447 | A | G | 2 | a0003c0003t0002g0076 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1051-216A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029447 | |||||||
chr18:13029576 | A | G | 67 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(64): Show |
69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1051-87A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 9/44 | chr18 | 13029576 | |||||||
chr18:13030084 | G | A | 10 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(7): Show |
10 | HG01109.hp2 HG02976.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+82G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030084 | |||||||
chr18:13030213 | C | G | 1 | a0031c0030t0001g0175 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1390+211C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030213 | |||||||
chr18:13030384 | G | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1391-81G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030384 | |||||||
chr18:13030437 | T | A | 1 | a0003c0003t0002g0092 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1391-28T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 10/44 | chr18 | 13030437 | |||||||
chr18:13030618 | T | C | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1534+10T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030618 | |||||||
chr18:13030734 | T | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1534+126T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030734 | |||||||
chr18:13030835 | A | G | 1 | a0004c0004t0001g0178 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1534+227A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030835 | |||||||
chr18:13030838 | T | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+230T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030838 | |||||||
chr18:13030887 | T | C | 1 | a0004c0004t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1534+279T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030887 | |||||||
chr18:13030955 | C | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+347C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030955 | |||||||
chr18:13030981 | AGT | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+377_1534+378d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13030981 | ||||||
chr18:13030984 | G | A | 1 | a0002c0001t0001g0337 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1534+376G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13030984 | |||||||
chr18:13031031 | CA | C | 11 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(8): Show |
11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1534+425delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031031 | ||||||
chr18:13031072 | A | T | 2 | a0004c0004t0001g0205 a0004c0004t0001g0206 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1534+464A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031072 | |||||||
chr18:13031157 | C | T | 2 | a0002c0001t0001g0292 a0002c0001t0001g0297 |
2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1534+549C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031157 | |||||||
chr18:13031243 | G | GT | 85 | a0001c0002t0001g0225 a0001c0002t0001g0232 a0001c0002t0001g0271 others(82): Show |
87 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1534+657dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | ||||||
chr18:13031243 | G | GTT | 26 | a0001c0002t0001g0263 a0002c0001t0001g0296 a0002c0001t0001g0322 others(23): Show |
27 | HG00140.hp1 HG00673.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1534+656_1534+657d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | ||||||
chr18:13031243 | GT | G | 47 | a0001c0002t0001g0209 a0002c0001t0001g0298 a0004c0004t0001g0001 others(44): Show |
58 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1534+657delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13031243 | ||||||
chr18:13031278 | C | T | 88 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(85): Show |
95 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1534+670C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031278 | |||||||
chr18:13031287 | G | A | 1 | a0009c0009t0001g0003 | 4 | HG00621.hp2 NA18970.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+679G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031287 | |||||||
chr18:13031489 | T | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+881T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031489 | |||||||
chr18:13031490 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+882G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031490 | |||||||
chr18:13031500 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+892G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031500 | |||||||
chr18:13031526 | C | T | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1534+918C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031526 | |||||||
chr18:13031539 | G | A | 1 | a0006c0006t0002g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1534+931G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031539 | |||||||
chr18:13031660 | G | A | 1 | a0009c0009t0001g0217 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1534+1052G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031660 | |||||||
chr18:13031991 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1534+1383C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13031991 | |||||||
chr18:13032277 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534+1669G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032277 | |||||||
chr18:13032484 | C | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+1876C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032484 | |||||||
chr18:13032537 | G | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1534+1929G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032537 | |||||||
chr18:13032541 | G | A | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1534+1933G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032541 | |||||||
chr18:13032623 | A | G | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1534+2015A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032623 | |||||||
chr18:13032667 | G | A | 2 | a0001c0002t0001g0260 a0001c0002t0001g0267 |
2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1534+2059G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032667 | |||||||
chr18:13032929 | C | T | 1 | a0028c0043t0001g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1534+2321C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032929 | |||||||
chr18:13032930 | ACT | A | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1534+2325_1534+232 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13032930 | ||||||
chr18:13032962 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1534+2354A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13032962 | |||||||
chr18:13033054 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1534+2446G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033054 | |||||||
chr18:13033148 | A | T | 2 | a0003c0003t0002g0052 a0003c0003t0002g0053 |
2 | HG00735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1534+2540A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033148 | |||||||
chr18:13033308 | C | T | 58 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(55): Show |
60 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1534+2700C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033308 | |||||||
chr18:13033471 | A | G | 1 | a0002c0001t0001g0293 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1534+2863A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033471 | |||||||
chr18:13033970 | T | A | 1 | a0003c0003t0002g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-3267T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033970 | |||||||
chr18:13033975 | G | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1535-3262G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033975 | |||||||
chr18:13033976 | T | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-3261T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13033976 | |||||||
chr18:13034409 | T | C | 1 | a0002c0001t0001g0299 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1535-2828T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034409 | |||||||
chr18:13034423 | G | A | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1535-2814G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034423 | |||||||
chr18:13034527 | G | A | 4 | a0005c0005t0001g0134 a0005c0005t0001g0135 a0005c0005t0001g0136 others(1): Show |
4 | HG00099.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-2710G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034527 | |||||||
chr18:13034603 | C | T | 1 | a0001c0002t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1535-2634C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034603 | |||||||
chr18:13034604 | G | A | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1535-2633G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034604 | |||||||
chr18:13034814 | G | A | 1 | a0007c0007t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1535-2423G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034814 | |||||||
chr18:13034820 | T | TA | 116 | a0001c0002t0001g0253 a0001c0002t0001g0273 a0001c0002t0001g0275 others(113): Show |
125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1535-2399dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13034820 | ||||||
chr18:13034922 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-2315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13034922 | |||||||
chr18:13035202 | T | C | 1 | a0005c0005t0001g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1535-2035T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035202 | |||||||
chr18:13035282 | T | C | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1535-1955T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035282 | |||||||
chr18:13035394 | G | C | 1 | a0033c0024t0001g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1535-1843G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035394 | |||||||
chr18:13035832 | G | A | 243 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1535-1405G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13035832 | |||||||
chr18:13036035 | T | G | 284 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(281): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1535-1202T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036035 | |||||||
chr18:13036145 | C | CA | 47 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0044t0001g0268 others(44): Show |
49 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1535-1079dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036145 | ||||||
chr18:13036151 | A | C | 1 | a0005c0005t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1535-1086A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036151 | |||||||
chr18:13036162 | TTTTG | T | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-1067_1535-106 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036162 | ||||||
chr18:13036178 | T | A | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.1535-1059T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036178 | |||||||
chr18:13036182 | A | T | 1 | a0001c0002t0001g0265 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1535-1055A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036182 | |||||||
chr18:13036255 | C | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-982C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036255 | |||||||
chr18:13036425 | C | T | 67 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(64): Show |
70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1535-812C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036425 | |||||||
chr18:13036639 | C | CCT | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1535-595_1535-594d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036639 | ||||||
chr18:13036681 | A | G | 1 | a0036c0035t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1535-556A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036681 | |||||||
chr18:13036748 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1535-489C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036748 | |||||||
chr18:13036781 | T | A | 20 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(17): Show |
20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-456T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036781 | |||||||
chr18:13036782 | C | T | 20 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(17): Show |
20 | HG01167.hp1 HG01884.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1535-455C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036782 | |||||||
chr18:13036875 | C | CTT | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1535-361_1535-360d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | INFO_REALIGN_3_PRIME | chr18 | 13036875 | ||||||
chr18:13036900 | A | C | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535-337A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036900 | |||||||
chr18:13036917 | A | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1535-320A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036917 | |||||||
chr18:13036947 | A | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-290A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13036947 | |||||||
chr18:13037019 | C | A | 287 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(284): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1535-218C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13037019 | |||||||
chr18:13037117 | G | A | 2 | a0003c0003t0002g0004 a0003c0003t0002g0065 |
4 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535-120G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 11/44 | chr18 | 13037117 | |||||||
chr18:13037433 | A | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1599+132A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037433 | |||||||
chr18:13037596 | C | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+295C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037596 | |||||||
chr18:13037696 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1599+395C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037696 | |||||||
chr18:13037698 | G | A | 1 | a0001c0033t0001g0210 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1599+397G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037698 | |||||||
chr18:13037830 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1599+529C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13037830 | |||||||
chr18:13038014 | A | C | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1600-356A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038014 | |||||||
chr18:13038195 | A | G | 1 | a0002c0001t0001g0317 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1600-175A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038195 | |||||||
chr18:13038202 | T | C | 1 | a0003c0003t0002g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1600-168T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038202 | |||||||
chr18:13038306 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1600-64A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 12/44 | chr18 | 13038306 | |||||||
chr18:13038635 | A | G | 1 | a0004c0004t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1809+56A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038635 | |||||||
chr18:13038786 | C | T | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+207C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038786 | |||||||
chr18:13038825 | T | A | 1 | a0002c0001t0001g0326 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1809+246T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13038825 | |||||||
chr18:13039054 | A | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1809+475A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039054 | |||||||
chr18:13039181 | G | T | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1809+602G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039181 | |||||||
chr18:13039230 | G | A | 1 | a0003c0003t0002g0008 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1809+651G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039230 | |||||||
chr18:13039262 | C | T | 66 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(63): Show |
68 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1809+683C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039262 | |||||||
chr18:13039263 | G | A | 1 | a0005c0005t0001g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1809+684G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039263 | |||||||
chr18:13039310 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1809+731C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039310 | |||||||
chr18:13039326 | G | A | 5 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(2): Show |
5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1809+747G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039326 | |||||||
chr18:13039424 | C | G | 67 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(64): Show |
69 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1809+845C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039424 | |||||||
chr18:13039455 | CA | C | 348 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(345): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1809+892delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chr18 | 13039455 | ||||||
chr18:13039455 | CAA | C | 6 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(3): Show |
6 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+891_1809+892d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chr18 | 13039455 | ||||||
chr18:13039753 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1810-1077G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039753 | |||||||
chr18:13039779 | C | T | 8 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(5): Show |
8 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1810-1051C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039779 | |||||||
chr18:13039828 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1810-1002G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13039828 | |||||||
chr18:13040085 | A | C | 108 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(105): Show |
117 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1810-745A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13040085 | |||||||
chr18:13040114 | T | C | 5 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(2): Show |
5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1810-716T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 13/44 | chr18 | 13040114 | |||||||
chr18:13041033 | G | A | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1936+77G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041033 | |||||||
chr18:13041050 | A | T | 1 | a0004c0004t0001g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1936+94A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041050 | |||||||
chr18:13041231 | G | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+275G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041231 | |||||||
chr18:13041303 | GATA | G | 4 | a0001c0002t0001g0245 a0001c0002t0001g0269 a0001c0002t0001g0272 others(1): Show |
4 | NA19001.hp1 NA19056.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+350_1936+352d others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041303 | ||||||
chr18:13041476 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1936+520G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041476 | |||||||
chr18:13041519 | A | G | 1 | a0002c0001t0001g0312 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1936+563A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041519 | |||||||
chr18:13041547 | C | G | 1 | a0005c0005t0001g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1936+591C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041547 | |||||||
chr18:13041580 | T | C | 1 | a0001c0002t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1936+624T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041580 | |||||||
chr18:13041581 | C | CT | 7 | a0001c0002t0001g0257 a0001c0002t0001g0259 a0002c0001t0001g0317 others(4): Show |
7 | HG02040.hp2 HG02056.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1937-609dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041581 | ||||||
chr18:13041581 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1937-623C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041581 | |||||||
chr18:13041581 | CT | C | 6 | a0001c0002t0001g0209 a0003c0003t0002g0045 a0014c0012t0001g0012 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-609delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | INFO_REALIGN_3_PRIME | chr18 | 13041581 | ||||||
chr18:13041787 | A | C | 5 | a0005c0005t0001g0014 a0005c0005t0001g0125 a0015c0014t0001g0013 others(2): Show |
6 | HG02132.hp1 NA18944.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1937-417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041787 | |||||||
chr18:13041831 | G | C | 41 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(38): Show |
43 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1937-373G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041831 | |||||||
chr18:13041856 | G | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1937-348G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041856 | |||||||
chr18:13041860 | C | A | 1 | a0002c0001t0001g0300 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1937-344C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13041860 | |||||||
chr18:13042143 | C | T | 1 | a0015c0014t0001g0013 | 2 | NA18944.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1937-61C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 14/44 | chr18 | 13042143 | |||||||
chr18:13042549 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2067+215A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042549 | |||||||
chr18:13042638 | C | T | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2067+304C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042638 | |||||||
chr18:13042639 | G | A | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.2067+305G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042639 | |||||||
chr18:13042931 | C | T | 1 | a0001c0002t0001g0262 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2067+597C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13042931 | |||||||
chr18:13043059 | G | A | 1 | a0007c0007t0002g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2067+725G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043059 | |||||||
chr18:13043729 | T | C | 1 | a0002c0001t0001g0319 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2067+1395T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043729 | |||||||
chr18:13043910 | T | C | 1 | a0002c0001t0001g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2067+1576T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043910 | |||||||
chr18:13043974 | C | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2067+1640C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13043974 | |||||||
chr18:13044015 | T | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2067+1681T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044015 | |||||||
chr18:13044093 | G | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2067+1759G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044093 | |||||||
chr18:13044262 | A | G | 6 | a0001c0002t0001g0220 a0001c0002t0001g0233 a0001c0002t0001g0248 others(3): Show |
6 | HG02129.hp2 NA18942.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.2067+1928A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044262 | |||||||
chr18:13044420 | T | TTTTTG | 114 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2067+2101_2067+210 others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13044420 | ||||||
chr18:13044683 | T | C | 1 | a0002c0023t0001g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2067+2349T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13044683 | |||||||
chr18:13045032 | T | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2067+2698T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045032 | |||||||
chr18:13045217 | C | T | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067+2883C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045217 | |||||||
chr18:13045321 | T | C | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2067+2987T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045321 | |||||||
chr18:13045563 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2067+3229G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045563 | |||||||
chr18:13045768 | G | A | 1 | a0001c0002t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2068-3091G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13045768 | |||||||
chr18:13046069 | G | A | 1 | a0001c0002t0001g0276 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2068-2790G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046069 | |||||||
chr18:13046078 | G | T | 1 | a0001c0002t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2068-2781G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046078 | |||||||
chr18:13046081 | C | G | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2068-2778C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046081 | |||||||
chr18:13046127 | G | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2068-2732G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046127 | |||||||
chr18:13046133 | G | A | 3 | a0005c0005t0001g0134 a0005c0005t0001g0135 a0005c0005t0001g0136 |
3 | HG00099.hp2 HG01099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2068-2726G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046133 | |||||||
chr18:13046146 | T | C | 114 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2068-2713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046146 | |||||||
chr18:13046147 | G | A | 1 | a0005c0005t0001g0126 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2068-2712G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046147 | |||||||
chr18:13046178 | G | A | 78 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(75): Show |
82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.2068-2681G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046178 | |||||||
chr18:13046260 | G | A | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2068-2599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046260 | |||||||
chr18:13046565 | A | G | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2068-2294A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046565 | |||||||
chr18:13046669 | A | G | 2 | a0014c0012t0001g0113 a0014c0012t0001g0114 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2068-2190A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046669 | |||||||
chr18:13046751 | A | T | 1 | a0001c0002t0001g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2068-2108A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046751 | |||||||
chr18:13046788 | C | G | 6 | a0003c0003t0002g0045 a0003c0003t0002g0071 a0003c0003t0002g0072 others(3): Show |
6 | HG00558.hp1 HG00597.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-2071C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046788 | |||||||
chr18:13046829 | C | CT | 74 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(71): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2068-2012dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | ||||||
chr18:13046829 | C | CTT | 42 | a0001c0002t0001g0227 a0001c0002t0001g0263 a0001c0002t0001g0273 others(39): Show |
44 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2068-2013_2068-201 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | ||||||
chr18:13046829 | CTTTTTTT | C | 6 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068-2018_2068-201 others(11): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13046829 | ||||||
chr18:13046847 | T | G | 1 | a0002c0001t0001g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2068-2012T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046847 | |||||||
chr18:13046920 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2068-1939A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13046920 | |||||||
chr18:13047209 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2068-1650C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047209 | |||||||
chr18:13047222 | T | C | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2068-1637T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047222 | |||||||
chr18:13047234 | A | G | 67 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(64): Show |
70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2068-1625A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047234 | |||||||
chr18:13047269 | C | T | 1 | a0003c0003t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2068-1590C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047269 | |||||||
chr18:13047271 | G | A | 2 | a0014c0012t0001g0012 a0025c0031t0001g0012 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2068-1588G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047271 | |||||||
chr18:13047295 | A | G | 2 | a0006c0006t0002g0042 a0006c0006t0002g0043 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2068-1564A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047295 | |||||||
chr18:13047360 | T | TAC | 29 | a0002c0001t0001g0022 a0004c0004t0001g0002 a0004c0004t0001g0195 others(26): Show |
35 | HG00642.hp1 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.2068-1482_2068-148 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13047360 | ||||||
chr18:13047360 | T | TACAC | 4 | a0001c0002t0001g0273 a0013c0016t0003g0215 a0013c0016t0003g0216 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-1484_2068-148 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13047360 | ||||||
chr18:13047552 | C | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2068-1307C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047552 | |||||||
chr18:13047785 | T | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2068-1074T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047785 | |||||||
chr18:13047786 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-1073C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047786 | |||||||
chr18:13047806 | T | C | 42 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(39): Show |
44 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2068-1053T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047806 | |||||||
chr18:13047819 | C | A | 4 | a0001c0002t0001g0240 a0001c0002t0001g0260 a0001c0002t0001g0267 others(1): Show |
4 | NA18950.hp1 NA18985.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068-1040C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047819 | |||||||
chr18:13047835 | C | G | 3 | a0005c0005t0001g0145 a0005c0005t0001g0161 a0005c0005t0001g0162 |
3 | HG01884.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2068-1024C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047835 | |||||||
chr18:13047984 | T | C | 114 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(111): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2068-875T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13047984 | |||||||
chr18:13048497 | C | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2068-362C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048497 | |||||||
chr18:13048534 | C | T | 1 | a0004c0004t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2068-325C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048534 | |||||||
chr18:13048571 | AT | A | 11 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(8): Show |
11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2068-286delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | INFO_REALIGN_3_PRIME | chr18 | 13048571 | ||||||
chr18:13048575 | C | A | 11 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(8): Show |
11 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2068-284C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048575 | |||||||
chr18:13048785 | A | G | 2 | a0005c0005t0001g0161 a0005c0005t0001g0162 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2068-74A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048785 | |||||||
chr18:13048797 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2068-62G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 15/44 | chr18 | 13048797 | |||||||
chr18:13049949 | G | A | 1 | a0001c0002t0001g0269 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3017+58G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13049949 | |||||||
chr18:13049949 | G | GA | 287 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(284): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3017+65dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13049949 | ||||||
chr18:13050048 | C | G | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+157C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050048 | |||||||
chr18:13050061 | C | CT | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3017+180dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13050061 | ||||||
chr18:13050147 | G | T | 3 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0002t0001g0258 |
3 | HG02040.hp2 NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.3017+256G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050147 | |||||||
chr18:13050170 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3017+279G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050170 | |||||||
chr18:13050390 | C | G | 82 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(79): Show |
89 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.3017+499C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050390 | |||||||
chr18:13050452 | C | T | 2 | a0001c0002t0001g0211 a0001c0033t0001g0210 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3017+561C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050452 | |||||||
chr18:13050533 | C | T | 2 | a0001c0002t0001g0211 a0001c0033t0001g0210 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3017+642C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050533 | |||||||
chr18:13050568 | T | G | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+677T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050568 | |||||||
chr18:13050575 | CT | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3017+696delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13050575 | ||||||
chr18:13050611 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3017+720G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050611 | |||||||
chr18:13050752 | G | A | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3017+861G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050752 | |||||||
chr18:13050883 | A | G | 1 | a0003c0003t0002g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3017+992A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050883 | |||||||
chr18:13050929 | G | A | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3017+1038G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050929 | |||||||
chr18:13050982 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3017+1091C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050982 | |||||||
chr18:13050996 | T | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.3017+1105T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13050996 | |||||||
chr18:13051138 | A | G | 1 | a0004c0004t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3017+1247A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051138 | |||||||
chr18:13051250 | A | G | 2 | a0016c0018t0002g0061 a0016c0018t0002g0091 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3017+1359A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051250 | |||||||
chr18:13051365 | T | TTG | 19 | a0005c0005t0001g0123 a0006c0006t0002g0026 a0006c0006t0002g0033 others(16): Show |
21 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.3017+1489_3017+149 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13051365 | ||||||
chr18:13051506 | T | C | 1 | a0005c0005t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3018-1413T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051506 | |||||||
chr18:13051612 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0032 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3018-1307C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051612 | |||||||
chr18:13051703 | C | G | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3018-1216C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051703 | |||||||
chr18:13051771 | C | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3018-1148C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051771 | |||||||
chr18:13051893 | C | T | 1 | a0003c0003t0002g0011 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3018-1026C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13051893 | |||||||
chr18:13052039 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3018-880C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052039 | |||||||
chr18:13052070 | G | A | 1 | a0001c0002t0001g0249 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3018-849G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052070 | |||||||
chr18:13052229 | A | G | 1 | a0002c0001t0001g0304 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3018-690A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052229 | |||||||
chr18:13052431 | T | C | 18 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(15): Show |
18 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.3018-488T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052431 | |||||||
chr18:13052474 | C | A | 78 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(75): Show |
82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3018-445C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052474 | |||||||
chr18:13052664 | C | T | 62 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(59): Show |
64 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.3018-255C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052664 | |||||||
chr18:13052689 | G | A | 1 | a0004c0004t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3018-230G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052689 | |||||||
chr18:13052829 | A | C | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3018-90A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052829 | |||||||
chr18:13052864 | T | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018-55T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052864 | |||||||
chr18:13052868 | G | T | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3018-51G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052868 | |||||||
chr18:13052895 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-24G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052895 | |||||||
chr18:13052896 | T | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-23T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052896 | |||||||
chr18:13052897 | G | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-22G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052897 | |||||||
chr18:13052898 | TGA | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-19_3018-18del others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr18 | 13052898 | ||||||
chr18:13052901 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-18G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052901 | |||||||
chr18:13052903 | T | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3018-16T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 17/44 | chr18 | 13052903 | |||||||
chr18:13053150 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3189+60A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053150 | |||||||
chr18:13053512 | G | A | 1 | a0005c0005t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3189+422G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053512 | |||||||
chr18:13053752 | C | T | 1 | a0005c0005t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3189+662C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13053752 | |||||||
chr18:13054104 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3189+1014A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054104 | |||||||
chr18:13054276 | A | G | 2 | a0004c0004t0001g0205 a0004c0004t0001g0206 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3189+1186A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054276 | |||||||
chr18:13054383 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.3189+1293G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054383 | |||||||
chr18:13054455 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.3190-1325T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054455 | |||||||
chr18:13054529 | T | G | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0044t0001g0268 |
3 | HG02451.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3190-1251T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054529 | |||||||
chr18:13054534 | A | G | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3190-1246A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054534 | |||||||
chr18:13054975 | C | T | 2 | a0002c0001t0001g0331 a0020c0025t0001g0295 |
2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3190-805C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13054975 | |||||||
chr18:13055183 | G | T | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3190-597G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055183 | |||||||
chr18:13055279 | C | CA | 9 | a0001c0002t0001g0227 a0001c0002t0001g0273 a0002c0001t0001g0359 others(6): Show |
9 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3190-484dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chr18 | 13055279 | ||||||
chr18:13055279 | CA | C | 16 | a0001c0002t0001g0239 a0004c0004t0001g0190 a0005c0005t0001g0150 others(13): Show |
16 | HG01515.hp1 HG01884.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.3190-484delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | INFO_REALIGN_3_PRIME | chr18 | 13055279 | ||||||
chr18:13055302 | C | T | 57 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(54): Show |
59 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.3190-478C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055302 | |||||||
chr18:13055400 | G | A | 1 | a0003c0003t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3190-380G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055400 | |||||||
chr18:13055402 | T | C | 1 | a0030c0041t0002g0106 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3190-378T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055402 | |||||||
chr18:13055513 | C | T | 1 | a0003c0003t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3190-267C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055513 | |||||||
chr18:13055766 | T | G | 2 | a0006c0006t0002g0033 a0006c0006t0002g0036 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3190-14T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 18/44 | chr18 | 13055766 | |||||||
chr18:13056852 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4108+154G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13056852 | |||||||
chr18:13056908 | A | G | 2 | a0003c0003t0002g0057 a0003c0003t0002g0110 |
2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.4108+210A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13056908 | |||||||
chr18:13057031 | C | G | 1 | a0006c0006t0002g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4108+333C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057031 | |||||||
chr18:13057046 | G | A | 7 | a0002c0001t0001g0305 a0002c0001t0001g0306 a0002c0001t0001g0311 others(4): Show |
7 | HG01361.hp1 HG01928.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.4108+348G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057046 | |||||||
chr18:13057065 | C | T | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4108+367C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057065 | |||||||
chr18:13057253 | G | GT | 40 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(37): Show |
42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4109-329dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | INFO_REALIGN_3_PRIME | chr18 | 13057253 | ||||||
chr18:13057253 | G | T | 6 | a0004c0004t0001g0015 a0004c0004t0001g0183 a0004c0004t0001g0187 others(3): Show |
7 | HG00621.hp1 NA18612.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.4109-332G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057253 | |||||||
chr18:13057257 | G | T | 40 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(37): Show |
42 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4109-328G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 19/44 | chr18 | 13057257 | |||||||
chr18:13057799 | C | T | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4257+66C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13057799 | |||||||
chr18:13057856 | T | C | 1 | a0002c0001t0001g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4257+123T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13057856 | |||||||
chr18:13058020 | T | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4257+287T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058020 | |||||||
chr18:13058319 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4257+586A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058319 | |||||||
chr18:13058407 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4257+674C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058407 | |||||||
chr18:13058460 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4258-622C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058460 | |||||||
chr18:13058495 | T | C | 239 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(236): Show |
253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.4258-587T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058495 | |||||||
chr18:13058503 | A | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4258-579A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058503 | |||||||
chr18:13058616 | G | A | 2 | a0002c0001t0001g0307 a0002c0001t0001g0310 |
2 | NA18945.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4258-466G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058616 | |||||||
chr18:13058837 | A | G | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0044t0001g0268 |
3 | HG02451.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4258-245A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058837 | |||||||
chr18:13058864 | A | T | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4258-218A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058864 | |||||||
chr18:13058870 | C | G | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4258-212C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058870 | |||||||
chr18:13058922 | C | T | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4258-160C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13058922 | |||||||
chr18:13059034 | T | C | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4258-48T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 20/44 | chr18 | 13059034 | |||||||
chr18:13059327 | A | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+15A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059327 | |||||||
chr18:13059373 | T | C | 34 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(31): Show |
36 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.4488+61T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059373 | |||||||
chr18:13059377 | A | C | 1 | a0001c0002t0001g0281 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4488+65A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059377 | |||||||
chr18:13059408 | G | A | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4488+96G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059408 | |||||||
chr18:13059495 | T | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4488+183T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059495 | |||||||
chr18:13059537 | A | G | 2 | a0005c0005t0001g0122 a0005c0005t0001g0123 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4488+225A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059537 | |||||||
chr18:13059539 | G | A | 1 | a0005c0005t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4488+227G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059539 | |||||||
chr18:13059876 | C | T | 13 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(10): Show |
13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.4488+564C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13059876 | |||||||
chr18:13060023 | G | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4488+711G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060023 | |||||||
chr18:13060080 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+768A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060080 | |||||||
chr18:13060144 | G | A | 1 | a0006c0006t0001g0355 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4488+832G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060144 | |||||||
chr18:13060181 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.4488+869G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060181 | |||||||
chr18:13060486 | G | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+1174G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060486 | |||||||
chr18:13060638 | ATT | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+1328_4488+132 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13060638 | ||||||
chr18:13060763 | A | T | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.4488+1451A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060763 | |||||||
chr18:13060799 | T | C | 1 | a0005c0005t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4488+1487T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060799 | |||||||
chr18:13060911 | G | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4488+1599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13060911 | |||||||
chr18:13060929 | GA | G | 277 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(274): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.4488+1629delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13060929 | ||||||
chr18:13061003 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+1691T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061003 | |||||||
chr18:13061013 | T | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+1701T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061013 | |||||||
chr18:13061089 | G | A | 1 | a0002c0001t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4488+1777G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061089 | |||||||
chr18:13061319 | C | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4488+2007C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061319 | |||||||
chr18:13061322 | GA | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4488+2018delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13061322 | ||||||
chr18:13061340 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4488+2028T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061340 | |||||||
chr18:13061542 | A | G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2230A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061542 | |||||||
chr18:13061668 | G | A | 1 | a0002c0001t0001g0323 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4488+2356G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061668 | |||||||
chr18:13061781 | A | G | 40 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(37): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.4488+2469A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061781 | |||||||
chr18:13061859 | G | A | 1 | a0002c0001t0001g0290 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4488+2547G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061859 | |||||||
chr18:13061995 | T | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2683T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13061995 | |||||||
chr18:13062074 | A | C | 1 | a0001c0002t0001g0277 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4488+2762A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062074 | |||||||
chr18:13062087 | C | T | 2 | a0008c0008t0001g0132 a0008c0008t0001g0168 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.4488+2775C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062087 | |||||||
chr18:13062102 | T | A | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4488+2790T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062102 | |||||||
chr18:13062135 | A | T | 2 | a0003c0003t0002g0049 a0030c0041t0002g0106 |
2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.4488+2823A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062135 | |||||||
chr18:13062228 | CT | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+2918delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062228 | ||||||
chr18:13062251 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+2939G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062251 | |||||||
chr18:13062414 | T | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4488+3102T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062414 | |||||||
chr18:13062486 | T | C | 2 | a0001c0002t0001g0261 a0001c0002t0001g0262 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4488+3174T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062486 | |||||||
chr18:13062526 | A | AT | 157 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(154): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.4488+3228dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062526 | ||||||
chr18:13062526 | AT | A | 43 | a0001c0002t0001g0245 a0003c0003t0002g0109 a0004c0004t0001g0001 others(40): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.4488+3228delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13062526 | ||||||
chr18:13062540 | T | A | 1 | a0001c0002t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4488+3228T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062540 | |||||||
chr18:13062572 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4488+3260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062572 | |||||||
chr18:13062920 | T | A | 1 | a0005c0005t0001g0016 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3608T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062920 | |||||||
chr18:13062946 | T | A | 1 | a0005c0005t0001g0016 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3634T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062946 | |||||||
chr18:13062952 | G | A | 1 | a0005c0005t0001g0016 | 2 | HG02071.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4488+3640G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13062952 | |||||||
chr18:13063085 | T | C | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4488+3773T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063085 | |||||||
chr18:13063096 | T | C | 1 | a0004c0004t0001g0181 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.4488+3784T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063096 | |||||||
chr18:13063127 | C | G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+3815C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063127 | |||||||
chr18:13063203 | C | G | 1 | a0010c0010t0002g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4488+3891C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063203 | |||||||
chr18:13063341 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4488+4029C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063341 | |||||||
chr18:13063475 | G | A | 11 | a0001c0002t0001g0017 a0001c0002t0001g0223 a0001c0002t0001g0224 others(8): Show |
12 | HG00544.hp2 HG02523.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.4488+4163G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063475 | |||||||
chr18:13063772 | T | A | 1 | a0005c0005t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4489-4059T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063772 | |||||||
chr18:13063820 | A | AT | 52 | a0001c0002t0001g0250 a0005c0005t0001g0014 a0005c0005t0001g0115 others(49): Show |
53 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.4489-3993dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13063820 | ||||||
chr18:13063890 | G | A | 17 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(14): Show |
17 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.4489-3941G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063890 | |||||||
chr18:13063892 | C | T | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4489-3939C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063892 | |||||||
chr18:13063897 | T | G | 6 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-3934T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13063897 | |||||||
chr18:13063995 | A | AT | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4489-3831dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13063995 | ||||||
chr18:13064089 | G | A | 1 | a0001c0002t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4489-3742G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064089 | |||||||
chr18:13064127 | T | G | 1 | a0004c0004t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4489-3704T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064127 | |||||||
chr18:13064440 | G | A | 2 | a0011c0011t0001g0282 a0011c0011t0001g0283 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4489-3391G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064440 | |||||||
chr18:13064480 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-3351C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064480 | |||||||
chr18:13064611 | C | CA | 57 | a0001c0002t0001g0225 a0001c0002t0001g0227 a0001c0002t0001g0246 others(54): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.4489-3201dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13064611 | ||||||
chr18:13064611 | CA | C | 22 | a0002c0001t0001g0287 a0003c0003t0002g0070 a0003c0003t0002g0074 others(19): Show |
22 | HG00558.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.4489-3201delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13064611 | ||||||
chr18:13064671 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4489-3160A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064671 | |||||||
chr18:13064861 | C | T | 1 | a0002c0001t0001g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4489-2970C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064861 | |||||||
chr18:13064879 | G | A | 77 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(74): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.4489-2952G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064879 | |||||||
chr18:13064879 | G | T | 1 | a0004c0004t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4489-2952G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13064879 | |||||||
chr18:13065096 | T | C | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4489-2735T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065096 | |||||||
chr18:13065175 | G | GT | 63 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(60): Show |
67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.4489-2644dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13065175 | ||||||
chr18:13065175 | G | T | 1 | a0002c0001t0001g0352 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4489-2656G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065175 | |||||||
chr18:13065178 | T | G | 2 | a0001c0002t0001g0261 a0001c0002t0001g0262 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4489-2653T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065178 | |||||||
chr18:13065290 | G | T | 1 | a0004c0004t0001g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4489-2541G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065290 | |||||||
chr18:13065352 | G | A | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-2479G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065352 | |||||||
chr18:13065361 | A | G | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4489-2470A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065361 | |||||||
chr18:13065364 | G | A | 1 | a0001c0002t0001g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4489-2467G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065364 | |||||||
chr18:13065485 | C | A | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4489-2346C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065485 | |||||||
chr18:13065549 | A | C | 8 | a0007c0007t0002g0006 a0007c0007t0002g0007 a0007c0007t0002g0024 others(5): Show |
10 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.4489-2282A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065549 | |||||||
chr18:13065549 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4489-2282A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065549 | |||||||
chr18:13065712 | A | G | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.4489-2119A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065712 | |||||||
chr18:13065729 | C | G | 13 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(10): Show |
13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.4489-2102C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065729 | |||||||
chr18:13065807 | A | C | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4489-2024A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065807 | |||||||
chr18:13065934 | G | A | 1 | a0001c0002t0001g0274 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4489-1897G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065934 | |||||||
chr18:13065987 | G | T | 1 | a0005c0005t0001g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4489-1844G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13065987 | |||||||
chr18:13066017 | A | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.4489-1814A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066017 | |||||||
chr18:13066039 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-1792G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066039 | |||||||
chr18:13066110 | C | G | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-1721C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066110 | |||||||
chr18:13066124 | T | C | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.4489-1707T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066124 | |||||||
chr18:13066365 | T | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-1466T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066365 | |||||||
chr18:13066511 | C | A | 1 | a0002c0001t0001g0349 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4489-1320C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066511 | |||||||
chr18:13066706 | G | C | 1 | a0005c0005t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4489-1125G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066706 | |||||||
chr18:13066790 | C | G | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.4489-1041C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066790 | |||||||
chr18:13066954 | T | G | 1 | a0002c0001t0001g0316 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4489-877T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13066954 | |||||||
chr18:13066963 | C | CTG | 84 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(81): Show |
96 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.4489-833_4489-832d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTG | 49 | a0002c0001t0001g0290 a0002c0001t0001g0305 a0002c0001t0001g0306 others(46): Show |
53 | HG00423.hp2 HG00621.hp1 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.4489-835_4489-832d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTG | 15 | a0002c0001t0001g0023 a0002c0001t0001g0316 a0002c0001t0001g0318 others(12): Show |
16 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.4489-837_4489-832d others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTGT others(1): Show |
22 | a0002c0001t0001g0315 a0002c0001t0001g0322 a0005c0005t0001g0016 others(19): Show |
23 | HG00597.hp1 HG00673.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.4489-839_4489-832d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTGT others(3): Show |
10 | a0005c0005t0001g0116 a0005c0005t0001g0124 a0005c0005t0001g0126 others(7): Show |
10 | HG00099.hp2 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.4489-841_4489-832d others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTGT others(5): Show |
20 | a0005c0005t0001g0014 a0005c0005t0001g0115 a0005c0005t0001g0125 others(17): Show |
24 | HG00621.hp2 HG02717.hp1 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.4489-843_4489-832d others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTGT others(7): Show |
5 | a0005c0005t0001g0152 a0005c0005t0001g0158 a0005c0005t0001g0171 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4489-845_4489-832d others(16): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | C | CTGTGTGT others(11): Show |
1 | a0033c0024t0001g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4489-849_4489-832d others(20): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066963 | CTG | C | 71 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(68): Show |
74 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.4489-833_4489-832d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066963 | ||||||
chr18:13066969 | G | GTGTGTGT others(5): Show |
8 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(5): Show |
8 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-851_4489-850i others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13066969 | ||||||
chr18:13067057 | A | C | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4489-774A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067057 | |||||||
chr18:13067124 | AT | A | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-700delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | INFO_REALIGN_3_PRIME | chr18 | 13067124 | ||||||
chr18:13067127 | T | A | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4489-704T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067127 | |||||||
chr18:13067139 | T | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4489-692T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067139 | |||||||
chr18:13067271 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-560G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067271 | |||||||
chr18:13067297 | G | A | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4489-534G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067297 | |||||||
chr18:13067369 | G | A | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4489-462G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067369 | |||||||
chr18:13067462 | A | T | 1 | a0010c0010t0002g0103 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4489-369A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067462 | |||||||
chr18:13067535 | T | C | 1 | a0001c0002t0001g0223 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4489-296T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067535 | |||||||
chr18:13067544 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-287G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067544 | |||||||
chr18:13067652 | G | T | 1 | a0001c0002t0001g0211 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4489-179G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067652 | |||||||
chr18:13067728 | G | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.4489-103G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067728 | |||||||
chr18:13067774 | A | G | 1 | a0003c0003t0002g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4489-57A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067774 | |||||||
chr18:13067802 | A | G | 2 | a0001c0002t0001g0261 a0001c0002t0001g0262 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4489-29A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 21/44 | chr18 | 13067802 | |||||||
chr18:13068324 | T | G | 5 | a0003c0003t0002g0076 a0003c0003t0002g0098 a0003c0003t0002g0102 others(2): Show |
5 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.4759-35T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/44 | chr18 | 13068324 | |||||||
chr18:13068340 | T | A | 5 | a0003c0003t0002g0076 a0003c0003t0002g0098 a0003c0003t0002g0102 others(2): Show |
5 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.4759-19T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 23/44 | chr18 | 13068340 | |||||||
chr18:13068429 | T | C | 1 | a0005c0005t0001g0120 | 1 | NA19064.hp1 | splice_region_variant&intron_variant | LOW | c.4822+7T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068429 | |||||||
chr18:13068577 | G | C | 1 | a0027c0045t0001g0333 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4822+155G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068577 | |||||||
chr18:13068612 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4822+190G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068612 | |||||||
chr18:13068694 | A | C | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.4823-158A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068694 | |||||||
chr18:13068715 | T | A | 3 | a0001c0002t0001g0209 a0001c0002t0001g0212 a0022c0021t0001g0346 |
3 | HG01109.hp2 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4823-137T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068715 | |||||||
chr18:13068726 | C | T | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4823-126C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068726 | |||||||
chr18:13068819 | G | A | 1 | a0013c0029t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4823-33G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 24/44 | chr18 | 13068819 | |||||||
chr18:13069006 | C | T | 1 | a0004c0004t0001g0178 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4962+15C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 25/44 | chr18 | 13069006 | |||||||
chr18:13069057 | C | T | 4 | a0012c0013t0002g0083 a0012c0013t0002g0096 a0012c0013t0002g0108 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4963-32C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 25/44 | chr18 | 13069057 | |||||||
chr18:13069222 | C | T | 46 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(43): Show |
56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.5055+41C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069222 | |||||||
chr18:13069329 | G | A | 1 | a0005c0005t0001g0120 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5055+148G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069329 | |||||||
chr18:13069468 | C | T | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5056-270C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069468 | |||||||
chr18:13069709 | T | C | 1 | a0005c0005t0001g0139 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5056-29T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 26/44 | chr18 | 13069709 | |||||||
chr18:13070120 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5174+264C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070120 | |||||||
chr18:13070156 | C | CA | 4 | a0002c0001t0001g0332 a0009c0009t0001g0003 a0009c0009t0001g0217 others(1): Show |
7 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.5174+312dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chr18 | 13070156 | ||||||
chr18:13070156 | CA | C | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5174+312delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | INFO_REALIGN_3_PRIME | chr18 | 13070156 | ||||||
chr18:13070528 | T | C | 1 | a0012c0013t0002g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5175-511T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070528 | |||||||
chr18:13070567 | C | T | 3 | a0001c0002t0001g0209 a0001c0002t0001g0212 a0022c0021t0001g0346 |
3 | HG01109.hp2 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.5175-472C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070567 | |||||||
chr18:13070712 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5175-327G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070712 | |||||||
chr18:13070713 | C | T | 3 | a0003c0003t0002g0011 a0003c0003t0002g0060 a0003c0003t0002g0085 |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.5175-326C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070713 | |||||||
chr18:13070724 | G | A | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5175-315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070724 | |||||||
chr18:13070754 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5175-285C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070754 | |||||||
chr18:13070852 | C | G | 1 | a0001c0002t0001g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5175-187C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070852 | |||||||
chr18:13070931 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.5175-108T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 27/44 | chr18 | 13070931 | |||||||
chr18:13071237 | G | A | 1 | a0003c0003t0002g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5348+25G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071237 | |||||||
chr18:13071321 | A | T | 1 | a0001c0002t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5348+109A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071321 | |||||||
chr18:13071353 | A | T | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.5348+141A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071353 | |||||||
chr18:13071385 | A | G | 1 | a0011c0011t0001g0353 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5348+173A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071385 | |||||||
chr18:13071396 | G | A | 1 | a0002c0001t0001g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5348+184G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071396 | |||||||
chr18:13071441 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5348+229G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071441 | |||||||
chr18:13071654 | T | C | 1 | a0011c0011t0001g0353 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5348+442T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071654 | |||||||
chr18:13071724 | G | GT | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5348+521dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chr18 | 13071724 | ||||||
chr18:13071752 | C | T | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5348+540C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071752 | |||||||
chr18:13071828 | A | G | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5348+616A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071828 | |||||||
chr18:13071975 | A | G | 1 | a0002c0001t0001g0347 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5348+763A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13071975 | |||||||
chr18:13072042 | G | A | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5349-713G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072042 | |||||||
chr18:13072110 | C | T | 5 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(2): Show |
5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.5349-645C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072110 | |||||||
chr18:13072380 | G | A | 1 | a0007c0007t0002g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5349-375G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072380 | |||||||
chr18:13072444 | A | T | 63 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(60): Show |
67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5349-311A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072444 | |||||||
chr18:13072479 | G | T | 1 | a0006c0006t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5349-276G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072479 | |||||||
chr18:13072560 | A | G | 1 | a0005c0005t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5349-195A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072560 | |||||||
chr18:13072583 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5349-172A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072583 | |||||||
chr18:13072703 | G | A | 76 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(73): Show |
79 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.5349-52G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 28/44 | chr18 | 13072703 | |||||||
chr18:13072959 | T | C | 1 | a0002c0001t0001g0304 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5440-50T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072959 | |||||||
chr18:13072964 | G | T | 2 | a0004c0004t0001g0177 a0004c0004t0001g0178 |
2 | NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5440-45G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072964 | |||||||
chr18:13072980 | T | C | 138 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(135): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.5440-29T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 29/44 | chr18 | 13072980 | |||||||
chr18:13073265 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5616+80C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073265 | |||||||
chr18:13073288 | C | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5616+103C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073288 | |||||||
chr18:13073386 | G | C | 1 | a0001c0002t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5616+201G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073386 | |||||||
chr18:13073533 | C | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+348C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073533 | |||||||
chr18:13073619 | C | G | 1 | a0001c0002t0001g0243 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5616+434C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073619 | |||||||
chr18:13073642 | C | T | 127 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(124): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.5616+457C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073642 | |||||||
chr18:13073703 | C | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+518C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073703 | |||||||
chr18:13073723 | G | A | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+538G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073723 | |||||||
chr18:13073776 | T | C | 1 | a0001c0002t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5616+591T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073776 | |||||||
chr18:13073809 | G | A | 1 | a0005c0005t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5616+624G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073809 | |||||||
chr18:13073864 | G | A | 1 | a0001c0002t0001g0240 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5616+679G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073864 | |||||||
chr18:13073866 | G | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+681G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073866 | |||||||
chr18:13073878 | G | A | 1 | a0005c0005t0001g0139 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5616+693G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13073878 | |||||||
chr18:13074014 | TAA | T | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5616+832_5616+833d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13074014 | ||||||
chr18:13074142 | TCTATATC | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+961_5616+967d others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13074142 | ||||||
chr18:13074143 | C | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+958C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074143 | |||||||
chr18:13074164 | G | A | 1 | a0007c0007t0002g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5616+979G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074164 | |||||||
chr18:13074240 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+1055C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074240 | |||||||
chr18:13074241 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+1056G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074241 | |||||||
chr18:13074352 | A | G | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5616+1167A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074352 | |||||||
chr18:13074395 | C | T | 3 | a0003c0003t0002g0063 a0003c0003t0002g0064 a0017c0017t0002g0010 |
4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+1210C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074395 | |||||||
chr18:13074396 | G | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+1211G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074396 | |||||||
chr18:13074418 | A | G | 2 | a0008c0008t0001g0132 a0008c0008t0001g0168 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.5616+1233A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074418 | |||||||
chr18:13074477 | C | G | 33 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(30): Show |
35 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.5616+1292C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074477 | |||||||
chr18:13074665 | A | G | 2 | a0003c0003t0002g0076 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.5616+1480A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074665 | |||||||
chr18:13074798 | G | A | 5 | a0004c0004t0001g0002 a0004c0004t0001g0184 a0004c0004t0001g0186 others(2): Show |
8 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+1613G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074798 | |||||||
chr18:13074837 | C | T | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5616+1652C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074837 | |||||||
chr18:13074851 | T | G | 1 | a0007c0007t0002g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5616+1666T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13074851 | |||||||
chr18:13075302 | CT | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+2118delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075302 | |||||||
chr18:13075458 | C | T | 1 | a0004c0004t0001g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5616+2273C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075458 | |||||||
chr18:13075552 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+2367G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075552 | |||||||
chr18:13075607 | C | T | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5616+2422C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075607 | |||||||
chr18:13075712 | A | T | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5616+2527A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075712 | |||||||
chr18:13075877 | A | T | 1 | a0004c0004t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5616+2692A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075877 | |||||||
chr18:13075999 | G | C | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.5616+2814G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13075999 | |||||||
chr18:13076133 | G | C | 1 | a0004c0004t0001g0192 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5616+2948G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076133 | |||||||
chr18:13076213 | T | C | 9 | a0006c0006t0002g0026 a0007c0007t0002g0006 a0007c0007t0002g0007 others(6): Show |
11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.5616+3028T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076213 | |||||||
chr18:13076251 | T | C | 78 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(75): Show |
81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5616+3066T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076251 | |||||||
chr18:13076297 | T | C | 2 | a0014c0012t0001g0012 a0025c0031t0001g0012 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.5616+3112T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076297 | |||||||
chr18:13076344 | C | T | 137 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(134): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.5616+3159C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076344 | |||||||
chr18:13076350 | G | A | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5616+3165G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076350 | |||||||
chr18:13076395 | TTG | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+3214_5616+321 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13076395 | ||||||
chr18:13076616 | C | G | 1 | a0003c0003t0002g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5616+3431C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076616 | |||||||
chr18:13076627 | G | C | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5616+3442G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076627 | |||||||
chr18:13076646 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+3461C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076646 | |||||||
chr18:13076663 | C | T | 1 | a0001c0002t0001g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5616+3478C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076663 | |||||||
chr18:13076664 | G | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+3479G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076664 | |||||||
chr18:13076664 | G | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+3479G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076664 | |||||||
chr18:13076795 | T | C | 1 | a0002c0001t0001g0348 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5616+3610T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076795 | |||||||
chr18:13076932 | C | T | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5616+3747C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076932 | |||||||
chr18:13076941 | A | G | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5616+3756A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13076941 | |||||||
chr18:13077185 | C | T | 1 | a0005c0005t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5616+4000C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077185 | |||||||
chr18:13077198 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5616+4013G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077198 | |||||||
chr18:13077213 | G | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5616+4028G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077213 | |||||||
chr18:13077316 | A | G | 131 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(128): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.5616+4131A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077316 | |||||||
chr18:13077729 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+4544G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077729 | |||||||
chr18:13077954 | CT | C | 235 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(232): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.5616+4773delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13077954 | ||||||
chr18:13077966 | G | T | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5616+4781G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077966 | |||||||
chr18:13077978 | C | A | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5616+4793C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13077978 | |||||||
chr18:13078103 | A | G | 4 | a0003c0003t0002g0008 a0003c0003t0002g0057 a0003c0003t0002g0058 others(1): Show |
5 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.5616+4918A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078103 | |||||||
chr18:13078307 | C | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5616+5122C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078307 | |||||||
chr18:13078540 | C | T | 1 | a0004c0004t0001g0200 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.5616+5355C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078540 | |||||||
chr18:13078597 | G | T | 1 | a0001c0002t0001g0245 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5616+5412G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078597 | |||||||
chr18:13078619 | G | A | 1 | a0020c0025t0001g0295 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5616+5434G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078619 | |||||||
chr18:13078633 | G | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5616+5448G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078633 | |||||||
chr18:13078682 | C | T | 24 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(21): Show |
26 | HG01167.hp1 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.5616+5497C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078682 | |||||||
chr18:13078742 | G | A | 1 | a0004c0004t0001g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5616+5557G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078742 | |||||||
chr18:13078750 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5616+5565C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078750 | |||||||
chr18:13078818 | G | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5616+5633G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078818 | |||||||
chr18:13078819 | A | T | 1 | a0005c0005t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5616+5634A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078819 | |||||||
chr18:13078849 | A | T | 1 | a0013c0016t0003g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5616+5664A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078849 | |||||||
chr18:13078987 | T | C | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5616+5802T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078987 | |||||||
chr18:13078996 | A | G | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5616+5811A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13078996 | |||||||
chr18:13079061 | A | G | 1 | a0004c0004t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5616+5876A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079061 | |||||||
chr18:13079086 | G | A | 1 | a0004c0004t0001g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5616+5901G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079086 | |||||||
chr18:13079345 | A | G | 77 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(74): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.5616+6160A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079345 | |||||||
chr18:13079457 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5616+6272A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079457 | |||||||
chr18:13079552 | G | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+6367G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079552 | |||||||
chr18:13079604 | G | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5616+6419G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079604 | |||||||
chr18:13079645 | A | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5616+6460A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079645 | |||||||
chr18:13079649 | C | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+6464C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079649 | |||||||
chr18:13079675 | C | T | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5616+6490C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079675 | |||||||
chr18:13079790 | A | C | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5616+6605A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079790 | |||||||
chr18:13079858 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5616+6673T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079858 | |||||||
chr18:13079911 | T | C | 1 | a0006c0006t0002g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5616+6726T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079911 | |||||||
chr18:13079993 | G | A | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5616+6808G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13079993 | |||||||
chr18:13080181 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6836C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080181 | |||||||
chr18:13080231 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6786G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080231 | |||||||
chr18:13080284 | C | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-6733C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080284 | |||||||
chr18:13080313 | T | C | 1 | a0010c0010t0002g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5617-6704T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080313 | |||||||
chr18:13080381 | T | A | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-6636T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080381 | |||||||
chr18:13080399 | A | C | 3 | a0003c0003t0002g0063 a0003c0003t0002g0064 a0017c0017t0002g0010 |
4 | HG02080.hp1 HG02083.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-6618A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080399 | |||||||
chr18:13080563 | T | C | 4 | a0002c0001t0001g0023 a0002c0001t0001g0318 a0002c0001t0001g0323 others(1): Show |
5 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-6454T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080563 | |||||||
chr18:13080890 | T | G | 78 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(75): Show |
81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5617-6127T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080890 | |||||||
chr18:13080970 | G | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-6047G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13080970 | |||||||
chr18:13081162 | G | A | 2 | a0001c0002t0001g0260 a0001c0002t0001g0267 |
2 | NA18985.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.5617-5855G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081162 | |||||||
chr18:13081304 | T | C | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5617-5713T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081304 | |||||||
chr18:13081322 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-5695T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081322 | |||||||
chr18:13081565 | G | C | 1 | a0004c0004t0001g0192 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5617-5452G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081565 | |||||||
chr18:13081614 | G | GT | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-5396dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13081614 | ||||||
chr18:13081795 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-5222G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081795 | |||||||
chr18:13081936 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-5081G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13081936 | |||||||
chr18:13082013 | T | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-5004T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082013 | |||||||
chr18:13082102 | C | G | 1 | a0010c0010t0002g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5617-4915C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082102 | |||||||
chr18:13082240 | A | G | 1 | a0002c0001t0001g0022 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.5617-4777A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082240 | |||||||
chr18:13082330 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4687C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082330 | |||||||
chr18:13082333 | T | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4684T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082333 | |||||||
chr18:13082432 | C | CT | 52 | a0001c0002t0001g0242 a0001c0002t0001g0280 a0002c0001t0001g0297 others(49): Show |
52 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.5617-4560dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | ||||||
chr18:13082432 | C | CTT | 18 | a0002c0001t0001g0298 a0002c0001t0001g0359 a0003c0003t0002g0049 others(15): Show |
22 | HG00741.hp2 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.5617-4561_5617-456 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | ||||||
chr18:13082432 | C | CTTT | 6 | a0004c0004t0001g0184 a0004c0004t0001g0199 a0014c0012t0001g0012 others(3): Show |
6 | HG00621.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-4562_5617-456 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | ||||||
chr18:13082432 | CT | C | 86 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(83): Show |
91 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5617-4560delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13082432 | ||||||
chr18:13082507 | A | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5617-4510A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082507 | |||||||
chr18:13082718 | G | A | 1 | a0004c0004t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5617-4299G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082718 | |||||||
chr18:13082783 | T | A | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5617-4234T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13082783 | |||||||
chr18:13083005 | T | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-4012T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083005 | |||||||
chr18:13083096 | G | A | 1 | a0004c0004t0001g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.5617-3921G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083096 | |||||||
chr18:13083198 | A | G | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5617-3819A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083198 | |||||||
chr18:13083389 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-3628C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083389 | |||||||
chr18:13083496 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3521A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083496 | |||||||
chr18:13083512 | C | T | 1 | a0002c0001t0001g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5617-3505C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083512 | |||||||
chr18:13083582 | G | A | 1 | a0003c0003t0002g0060 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5617-3435G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083582 | |||||||
chr18:13083644 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3373A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083644 | |||||||
chr18:13083673 | C | T | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5617-3344C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083673 | |||||||
chr18:13083685 | G | A | 1 | a0002c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5617-3332G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083685 | |||||||
chr18:13083868 | T | A | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-3149T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13083868 | |||||||
chr18:13084059 | G | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2958G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084059 | |||||||
chr18:13084116 | G | A | 1 | a0001c0002t0001g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5617-2901G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084116 | |||||||
chr18:13084164 | A | G | 1 | a0001c0002t0001g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5617-2853A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084164 | |||||||
chr18:13084266 | G | A | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2751G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084266 | |||||||
chr18:13084337 | C | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-2680C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084337 | |||||||
chr18:13084383 | CT | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-2633delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084383 | |||||||
chr18:13084385 | G | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-2632G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084385 | |||||||
chr18:13084434 | C | T | 42 | a0001c0002t0001g0221 a0004c0004t0001g0001 a0004c0004t0001g0002 others(39): Show |
52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.5617-2583C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084434 | |||||||
chr18:13084435 | G | A | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-2582G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084435 | |||||||
chr18:13084496 | C | T | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.5617-2521C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084496 | |||||||
chr18:13084559 | C | T | 5 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(2): Show |
5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2458C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084559 | |||||||
chr18:13084564 | G | A | 1 | a0002c0022t0001g0302 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.5617-2453G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084564 | |||||||
chr18:13084711 | C | T | 1 | a0002c0001t0001g0323 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5617-2306C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084711 | |||||||
chr18:13084729 | G | A | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5617-2288G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084729 | |||||||
chr18:13084762 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-2255G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084762 | |||||||
chr18:13084786 | G | A | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-2231G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084786 | |||||||
chr18:13084820 | C | CT | 73 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0031 others(70): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.5617-2186dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084820 | ||||||
chr18:13084904 | C | T | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.5617-2113C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084904 | |||||||
chr18:13084961 | G | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5617-2056G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084961 | |||||||
chr18:13084981 | A | G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.5617-2036A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13084981 | |||||||
chr18:13084991 | G | GT | 11 | a0002c0001t0001g0310 a0002c0001t0001g0359 a0003c0003t0002g0105 others(8): Show |
11 | HG01515.hp1 HG02145.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.5617-2012dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084991 | ||||||
chr18:13084991 | GT | G | 7 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(4): Show |
7 | HG01167.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.5617-2012delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13084991 | ||||||
chr18:13085114 | C | T | 1 | a0002c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5617-1903C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085114 | |||||||
chr18:13085115 | G | A | 1 | a0005c0005t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5617-1902G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085115 | |||||||
chr18:13085121 | G | A | 1 | a0003c0003t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5617-1896G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085121 | |||||||
chr18:13085130 | G | A | 127 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(124): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.5617-1887G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085130 | |||||||
chr18:13085170 | G | A | 1 | a0001c0002t0001g0278 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.5617-1847G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085170 | |||||||
chr18:13085175 | T | C | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5617-1842T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085175 | |||||||
chr18:13085237 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.5617-1780G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085237 | |||||||
chr18:13085383 | GA | G | 133 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(130): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.5617-1632delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085383 | ||||||
chr18:13085438 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-1579G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085438 | |||||||
chr18:13085472 | G | A | 1 | a0011c0011t0001g0353 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5617-1545G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085472 | |||||||
chr18:13085473 | T | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5617-1544T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085473 | |||||||
chr18:13085496 | T | G | 63 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(60): Show |
67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5617-1521T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085496 | |||||||
chr18:13085756 | T | TCTGTTTT others(15): Show |
3 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0002t0001g0258 |
3 | HG02040.hp2 NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.5617-1250_5617-122 others(26): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085756 | ||||||
chr18:13085804 | G | T | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-1213G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085804 | |||||||
chr18:13085825 | C | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5617-1192C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085825 | |||||||
chr18:13085874 | C | T | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.5617-1143C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085874 | |||||||
chr18:13085910 | G | GT | 5 | a0003c0003t0002g0107 a0009c0009t0001g0003 a0009c0009t0001g0217 others(2): Show |
8 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.5617-1097dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13085910 | ||||||
chr18:13085998 | A | G | 1 | a0033c0024t0001g0358 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5617-1019A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13085998 | |||||||
chr18:13086032 | C | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5617-985C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086032 | |||||||
chr18:13086335 | A | C | 1 | a0002c0023t0001g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5617-682A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086335 | |||||||
chr18:13086365 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5617-652G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086365 | |||||||
chr18:13086476 | G | T | 1 | a0001c0002t0001g0267 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5617-541G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086476 | |||||||
chr18:13086620 | T | C | 1 | a0006c0006t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5617-397T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086620 | |||||||
chr18:13086703 | C | CTA | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.5617-311_5617-310d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | INFO_REALIGN_3_PRIME | chr18 | 13086703 | ||||||
chr18:13086742 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5617-275A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086742 | |||||||
chr18:13086947 | C | T | 1 | a0002c0001t0001g0304 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5617-70C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 30/44 | chr18 | 13086947 | |||||||
chr18:13087286 | A | G | 3 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 |
3 | HG02630.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5877+9A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087286 | |||||||
chr18:13087405 | T | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5878-126T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087405 | |||||||
chr18:13087454 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5878-77C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 31/44 | chr18 | 13087454 | |||||||
chr18:13087790 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.5993+144A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087790 | |||||||
chr18:13087816 | G | A | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.5993+170G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087816 | |||||||
chr18:13087824 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5993+178C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087824 | |||||||
chr18:13087960 | A | G | 1 | a0004c0004t0001g0203 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5993+314A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13087960 | |||||||
chr18:13088059 | C | T | 1 | a0001c0002t0001g0257 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5993+413C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088059 | |||||||
chr18:13088082 | A | G | 35 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(32): Show |
37 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.5993+436A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088082 | |||||||
chr18:13088157 | T | G | 2 | a0003c0003t0002g0076 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.5993+511T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088157 | |||||||
chr18:13088319 | G | A | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.5993+673G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088319 | |||||||
chr18:13088526 | T | A | 1 | a0003c0003t0006g0099 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5993+880T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088526 | |||||||
chr18:13088667 | C | T | 2 | a0001c0002t0001g0243 a0002c0001t0001g0286 |
2 | HG01081.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.5994-789C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088667 | |||||||
chr18:13088674 | T | C | 243 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(240): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.5994-782T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088674 | |||||||
chr18:13088681 | T | C | 1 | a0035c0028t0001g0356 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5994-775T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088681 | |||||||
chr18:13088895 | A | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5994-561A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088895 | |||||||
chr18:13088916 | T | G | 2 | a0004c0004t0001g0002 a0004c0004t0001g0195 |
5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.5994-540T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088916 | |||||||
chr18:13088931 | A | G | 2 | a0002c0001t0001g0331 a0020c0025t0001g0295 |
2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5994-525A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13088931 | |||||||
chr18:13089030 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.5994-426C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089030 | |||||||
chr18:13089039 | A | C | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5994-417A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089039 | |||||||
chr18:13089149 | A | G | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.5994-307A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089149 | |||||||
chr18:13089280 | T | C | 1 | a0003c0003t0002g0066 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5994-176T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089280 | |||||||
chr18:13089355 | A | G | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.5994-101A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089355 | |||||||
chr18:13089373 | C | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.5994-83C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089373 | |||||||
chr18:13089441 | A | T | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.5994-15A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 32/44 | chr18 | 13089441 | |||||||
chr18:13089580 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6103+15G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089580 | |||||||
chr18:13089786 | C | G | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6103+221C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089786 | |||||||
chr18:13089825 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6103+260A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089825 | |||||||
chr18:13089909 | T | A | 1 | a0001c0002t0001g0277 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.6103+344T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13089909 | |||||||
chr18:13090506 | G | A | 32 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(29): Show |
34 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.6103+941G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090506 | |||||||
chr18:13090668 | C | A | 133 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(130): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.6103+1103C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090668 | |||||||
chr18:13090686 | G | A | 1 | a0004c0004t0001g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6103+1121G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090686 | |||||||
chr18:13090829 | A | G | 1 | a0005c0005t0001g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6103+1264A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090829 | |||||||
chr18:13090951 | G | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6103+1386G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090951 | |||||||
chr18:13090983 | A | G | 137 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(134): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.6104-1394A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13090983 | |||||||
chr18:13091250 | A | G | 1 | a0010c0010t0002g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6104-1127A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091250 | |||||||
chr18:13091402 | A | G | 1 | a0001c0002t0001g0269 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.6104-975A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091402 | |||||||
chr18:13091454 | G | A | 1 | a0002c0001t0001g0303 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6104-923G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091454 | |||||||
chr18:13091471 | G | GT | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.6104-906_6104-905i others(3): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091471 | |||||||
chr18:13091479 | A | C | 5 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.6104-898A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091479 | |||||||
chr18:13091523 | T | C | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6104-854T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091523 | |||||||
chr18:13091662 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6104-715T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091662 | |||||||
chr18:13091965 | A | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6104-412A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091965 | |||||||
chr18:13091989 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6104-388A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13091989 | |||||||
chr18:13092025 | G | A | 3 | a0003c0003t0002g0095 a0019c0015t0002g0039 a0019c0015t0002g0040 |
3 | HG02895.hp1 HG02897.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.6104-352G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092025 | |||||||
chr18:13092162 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6104-215A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092162 | |||||||
chr18:13092220 | G | A | 1 | a0001c0002t0001g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6104-157G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092220 | |||||||
chr18:13092243 | C | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6104-134C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092243 | |||||||
chr18:13092274 | A | G | 1 | a0004c0004t0001g0178 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.6104-103A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092274 | |||||||
chr18:13092290 | A | G | 1 | a0002c0001t0001g0312 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6104-87A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 33/44 | chr18 | 13092290 | |||||||
chr18:13092770 | T | G | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+243T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092770 | |||||||
chr18:13092777 | C | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+250C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092777 | |||||||
chr18:13092857 | A | G | 3 | a0005c0005t0001g0137 a0005c0005t0001g0169 a0005c0005t0001g0170 |
3 | NA18956.hp2 NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.6254+330A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092857 | |||||||
chr18:13092951 | G | A | 3 | a0002c0001t0001g0319 a0002c0001t0001g0320 a0002c0001t0001g0326 |
3 | NA18998.hp1 NA19004.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.6254+424G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13092951 | |||||||
chr18:13093190 | C | T | 1 | a0036c0035t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6254+663C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093190 | |||||||
chr18:13093337 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6254+810C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093337 | |||||||
chr18:13093354 | T | C | 12 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(9): Show |
12 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.6254+827T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093354 | |||||||
chr18:13093366 | C | T | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.6254+839C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093366 | |||||||
chr18:13093384 | C | T | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.6254+857C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093384 | |||||||
chr18:13093424 | C | T | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.6254+897C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093424 | |||||||
chr18:13093426 | G | T | 2 | a0001c0002t0001g0211 a0001c0033t0001g0210 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.6254+899G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093426 | |||||||
chr18:13093522 | A | G | 33 | a0005c0005t0001g0014 a0005c0005t0001g0016 a0005c0005t0001g0115 others(30): Show |
35 | HG00099.hp2 HG00597.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.6254+995A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093522 | |||||||
chr18:13093712 | T | C | 2 | a0001c0002t0001g0211 a0001c0033t0001g0210 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.6254+1185T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093712 | |||||||
chr18:13093775 | G | A | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6254+1248G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093775 | |||||||
chr18:13093797 | G | A | 235 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(232): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.6254+1270G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093797 | |||||||
chr18:13093943 | G | A | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6254+1416G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13093943 | |||||||
chr18:13094017 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6255-1486C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094017 | |||||||
chr18:13094045 | G | T | 1 | a0003c0003t0002g0060 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6255-1458G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094045 | |||||||
chr18:13094133 | G | A | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6255-1370G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094133 | |||||||
chr18:13094291 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6255-1212C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094291 | |||||||
chr18:13094802 | C | T | 214 | a0002c0001t0001g0020 a0002c0001t0001g0022 a0002c0001t0001g0023 others(211): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.6255-701C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094802 | |||||||
chr18:13094805 | C | T | 1 | a0003c0003t0002g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6255-698C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094805 | |||||||
chr18:13094821 | AC | A | 128 | a0002c0001t0001g0020 a0002c0001t0001g0022 a0002c0001t0001g0023 others(125): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.6255-680delC | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chr18 | 13094821 | ||||||
chr18:13094885 | C | A | 75 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(72): Show |
78 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.6255-618C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094885 | |||||||
chr18:13094997 | A | G | 4 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(1): Show |
4 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.6255-506A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13094997 | |||||||
chr18:13095109 | T | C | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6255-394T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095109 | |||||||
chr18:13095131 | G | C | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6255-372G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095131 | |||||||
chr18:13095196 | C | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6255-307C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095196 | |||||||
chr18:13095212 | G | A | 1 | a0009c0009t0001g0003 | 4 | HG00621.hp2 NA18970.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.6255-291G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095212 | |||||||
chr18:13095249 | G | A | 4 | a0001c0002t0001g0239 a0001c0002t0001g0242 a0001c0002t0001g0243 others(1): Show |
4 | NA18946.hp1 NA18984.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.6255-254G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095249 | |||||||
chr18:13095293 | C | T | 1 | a0001c0002t0001g0225 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.6255-210C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095293 | |||||||
chr18:13095319 | A | G | 4 | a0002c0001t0001g0023 a0002c0001t0001g0318 a0002c0001t0001g0323 others(1): Show |
5 | HG01099.hp1 HG01261.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.6255-184A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095319 | |||||||
chr18:13095402 | A | T | 127 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(124): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.6255-101A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095402 | |||||||
chr18:13095477 | T | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6255-26T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 34/44 | chr18 | 13095477 | |||||||
chr18:13095726 | C | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6433+45C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | chr18 | 13095726 | |||||||
chr18:13095988 | C | A | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6434-196C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | chr18 | 13095988 | |||||||
chr18:13095989 | CAAGCAGT others(1): Show |
C | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6434-193_6434-186d others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 35/44 | INFO_REALIGN_3_PRIME | chr18 | 13095989 | ||||||
chr18:13096404 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+97G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096404 | |||||||
chr18:13096437 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6557+130T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096437 | |||||||
chr18:13096689 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6557+382C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096689 | |||||||
chr18:13096704 | G | T | 1 | a0001c0002t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6557+397G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096704 | |||||||
chr18:13096713 | G | A | 1 | a0002c0001t0001g0340 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6557+406G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096713 | |||||||
chr18:13096726 | G | C | 1 | a0006c0006t0002g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6557+419G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096726 | |||||||
chr18:13096818 | C | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+511C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13096818 | |||||||
chr18:13097208 | C | T | 133 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(130): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.6557+901C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097208 | |||||||
chr18:13097411 | A | T | 1 | a0003c0003t0002g0092 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6557+1104A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097411 | |||||||
chr18:13097523 | C | G | 7 | a0007c0007t0002g0006 a0007c0007t0002g0007 a0007c0007t0002g0025 others(4): Show |
9 | HG01952.hp2 HG02486.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.6557+1216C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097523 | |||||||
chr18:13097528 | G | C | 1 | a0002c0001t0001g0318 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.6557+1221G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097528 | |||||||
chr18:13097627 | CT | C | 7 | a0001c0002t0001g0228 a0001c0002t0001g0258 a0001c0002t0001g0271 others(4): Show |
7 | HG00673.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6557+1334delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13097627 | ||||||
chr18:13097649 | AT | A | 7 | a0005c0005t0001g0133 a0006c0006t0001g0355 a0006c0006t0001g0357 others(4): Show |
7 | HG01515.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.6557+1356delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13097649 | ||||||
chr18:13097651 | T | TA | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6557+1344_6557+134 others(5): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097651 | |||||||
chr18:13097652 | T | A | 67 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(64): Show |
71 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.6557+1345T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097652 | |||||||
chr18:13097655 | T | A | 5 | a0002c0001t0001g0304 a0014c0012t0001g0012 a0014c0012t0001g0113 others(2): Show |
5 | HG01256.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.6557+1348T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097655 | |||||||
chr18:13097728 | G | A | 1 | a0007c0007t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6557+1421G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097728 | |||||||
chr18:13097789 | A | C | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.6557+1482A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097789 | |||||||
chr18:13097838 | C | T | 75 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(72): Show |
78 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.6557+1531C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097838 | |||||||
chr18:13097854 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6557+1547A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097854 | |||||||
chr18:13097869 | G | A | 7 | a0002c0001t0001g0298 a0002c0001t0001g0299 a0002c0001t0001g0300 others(4): Show |
7 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.6557+1562G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13097869 | |||||||
chr18:13098012 | A | G | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-1464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098012 | |||||||
chr18:13098071 | G | A | 2 | a0004c0004t0001g0190 a0004c0004t0001g0193 |
2 | NA18993.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.6558-1405G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098071 | |||||||
chr18:13098120 | C | T | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-1356C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098120 | |||||||
chr18:13098139 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-1337C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098139 | |||||||
chr18:13098174 | G | A | 6 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(3): Show |
6 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.6558-1302G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098174 | |||||||
chr18:13098194 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-1282G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098194 | |||||||
chr18:13098206 | T | G | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-1270T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098206 | |||||||
chr18:13098247 | G | C | 1 | a0002c0001t0001g0316 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6558-1229G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098247 | |||||||
chr18:13098297 | T | G | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-1179T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098297 | |||||||
chr18:13098359 | C | T | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-1117C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098359 | |||||||
chr18:13098406 | GCTCCTCA others(33): Show |
G | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.6558-1042_6558-100 others(44): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098406 | ||||||
chr18:13098440 | G | A | 5 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(2): Show |
8 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.6558-1036G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098440 | |||||||
chr18:13098482 | CGCTCCTC others(109): Show |
C | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6558-984_6558-869d others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098482 | ||||||
chr18:13098513 | G | A | 6 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(3): Show |
6 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.6558-963G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098513 | |||||||
chr18:13098584 | C | T | 4 | a0004c0004t0001g0015 a0004c0004t0001g0183 a0004c0004t0001g0187 others(1): Show |
5 | NA18949.hp1 NA18965.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.6558-892C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098584 | |||||||
chr18:13098586 | G | T | 1 | a0005c0005t0001g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.6558-890G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098586 | |||||||
chr18:13098598 | T | C | 287 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(284): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.6558-878T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098598 | |||||||
chr18:13098599 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-877G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098599 | |||||||
chr18:13098639 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.6558-837G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098639 | |||||||
chr18:13098678 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6558-798C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098678 | |||||||
chr18:13098722 | C | G | 1 | a0005c0005t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6558-754C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098722 | |||||||
chr18:13098752 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-724G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098752 | |||||||
chr18:13098768 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6558-708C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098768 | |||||||
chr18:13098772 | C | CG | 12 | a0001c0002t0001g0250 a0001c0002t0001g0253 a0001c0002t0001g0255 others(9): Show |
12 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.6558-700dupG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13098772 | ||||||
chr18:13098785 | G | A | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.6558-691G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098785 | |||||||
chr18:13098864 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6558-612C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098864 | |||||||
chr18:13098907 | C | T | 1 | a0002c0001t0001g0306 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6558-569C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098907 | |||||||
chr18:13098927 | C | T | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6558-549C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098927 | |||||||
chr18:13098935 | C | T | 1 | a0003c0003t0002g0068 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.6558-541C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13098935 | |||||||
chr18:13099006 | C | T | 1 | a0002c0001t0001g0316 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6558-470C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099006 | |||||||
chr18:13099041 | G | A | 1 | a0003c0003t0002g0011 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6558-435G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099041 | |||||||
chr18:13099049 | G | A | 2 | a0004c0004t0001g0177 a0004c0004t0001g0178 |
2 | NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.6558-427G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099049 | |||||||
chr18:13099060 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-416A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099060 | |||||||
chr18:13099102 | G | C | 1 | a0002c0001t0001g0303 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6558-374G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099102 | |||||||
chr18:13099130 | G | A | 1 | a0032c0037t0002g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6558-346G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099130 | |||||||
chr18:13099149 | C | G | 1 | a0001c0002t0001g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6558-327C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099149 | |||||||
chr18:13099161 | G | A | 1 | a0008c0008t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6558-315G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099161 | |||||||
chr18:13099175 | AGGGAGG | A | 3 | a0001c0044t0001g0268 a0019c0015t0002g0039 a0019c0015t0002g0040 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6558-283_6558-278d others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | INFO_REALIGN_3_PRIME | chr18 | 13099175 | ||||||
chr18:13099199 | A | G | 2 | a0001c0002t0001g0275 a0001c0002t0001g0278 |
2 | NA18956.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.6558-277A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099199 | |||||||
chr18:13099250 | C | T | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.6558-226C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099250 | |||||||
chr18:13099283 | C | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6558-193C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099283 | |||||||
chr18:13099323 | C | T | 1 | a0004c0004t0001g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6558-153C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 36/44 | chr18 | 13099323 | |||||||
chr18:13099700 | A | G | 1 | a0004c0004t0001g0196 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.6663+119A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13099700 | |||||||
chr18:13099824 | A | G | 2 | a0001c0002t0001g0209 a0001c0002t0001g0212 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.6663+243A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13099824 | |||||||
chr18:13100006 | G | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6664-299G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100006 | |||||||
chr18:13100011 | T | C | 2 | a0004c0004t0001g0205 a0004c0004t0001g0206 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.6664-294T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100011 | |||||||
chr18:13100099 | G | A | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6664-206G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100099 | |||||||
chr18:13100252 | G | A | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6664-53G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 37/44 | chr18 | 13100252 | |||||||
chr18:13100663 | T | C | 1 | a0006c0006t0001g0357 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6871+151T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100663 | |||||||
chr18:13100723 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6871+211G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100723 | |||||||
chr18:13100770 | G | A | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6871+258G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13100770 | |||||||
chr18:13101143 | C | T | 1 | a0003c0003t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6871+631C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101143 | |||||||
chr18:13101161 | T | A | 1 | a0005c0005t0001g0126 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.6871+649T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101161 | |||||||
chr18:13101169 | A | G | 280 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.6871+657A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101169 | |||||||
chr18:13101228 | A | G | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.6871+716A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101228 | |||||||
chr18:13101253 | A | G | 2 | a0005c0005t0001g0161 a0005c0005t0001g0162 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.6871+741A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101253 | |||||||
chr18:13101372 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6871+860G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101372 | |||||||
chr18:13101435 | A | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6871+923A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101435 | |||||||
chr18:13101471 | T | C | 5 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(2): Show |
5 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.6871+959T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101471 | |||||||
chr18:13101510 | G | A | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.6871+998G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101510 | |||||||
chr18:13101652 | A | G | 1 | a0003c0003t0002g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6871+1140A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101652 | |||||||
chr18:13101761 | C | T | 1 | a0002c0001t0001g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6871+1249C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101761 | |||||||
chr18:13101903 | T | G | 137 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(134): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.6871+1391T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13101903 | |||||||
chr18:13102005 | C | T | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6871+1493C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102005 | |||||||
chr18:13102329 | G | A | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.6872-1180G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102329 | |||||||
chr18:13102405 | C | G | 5 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(2): Show |
5 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6872-1104C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102405 | |||||||
chr18:13102473 | A | G | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6872-1036A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102473 | |||||||
chr18:13102825 | C | A | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6872-684C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102825 | |||||||
chr18:13102842 | T | C | 1 | a0004c0004t0001g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6872-667T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102842 | |||||||
chr18:13102861 | A | G | 2 | a0003c0003t0002g0049 a0030c0041t0002g0106 |
2 | HG02074.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.6872-648A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102861 | |||||||
chr18:13102958 | G | T | 1 | a0002c0001t0001g0359 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6872-551G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13102958 | |||||||
chr18:13103310 | A | C | 1 | a0005c0005t0001g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6872-199A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13103310 | |||||||
chr18:13103328 | A | G | 1 | a0003c0003t0002g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6872-181A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 38/44 | chr18 | 13103328 | |||||||
chr18:13103661 | A | G | 5 | a0003c0003t0002g0044 a0009c0009t0001g0003 a0009c0009t0001g0217 others(2): Show |
8 | HG00621.hp2 HG02129.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.6951+73A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13103661 | |||||||
chr18:13103815 | A | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.6951+227A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13103815 | |||||||
chr18:13104042 | G | A | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6951+454G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104042 | |||||||
chr18:13104252 | A | C | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6951+664A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104252 | |||||||
chr18:13104252 | A | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.6951+664A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104252 | |||||||
chr18:13104330 | AGTCT | A | 63 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(60): Show |
67 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.6952-653_6952-650d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104330 | |||||||
chr18:13104544 | C | T | 2 | a0005c0005t0001g0143 a0005c0005t0001g0144 |
2 | NA18982.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.6952-440C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104544 | |||||||
chr18:13104618 | AT | A | 4 | a0005c0005t0001g0115 a0005c0005t0001g0116 a0005c0005t0001g0127 others(1): Show |
4 | HG01071.hp2 HG01255.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.6952-365delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104618 | |||||||
chr18:13104687 | A | C | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6952-297A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104687 | |||||||
chr18:13104901 | G | A | 4 | a0001c0002t0001g0266 a0001c0002t0001g0274 a0006c0006t0001g0355 others(1): Show |
4 | HG01192.hp2 HG01515.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.6952-83G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 39/44 | chr18 | 13104901 | |||||||
chr18:13105336 | A | G | 2 | a0004c0004t0001g0205 a0004c0004t0001g0206 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.7047+257A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105336 | |||||||
chr18:13105364 | G | A | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7047+285G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105364 | |||||||
chr18:13105450 | C | T | 1 | a0002c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7047+371C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105450 | |||||||
chr18:13105541 | G | A | 62 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(59): Show |
66 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.7047+462G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105541 | |||||||
chr18:13105572 | C | T | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7047+493C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105572 | |||||||
chr18:13105651 | G | A | 5 | a0004c0004t0001g0173 a0004c0004t0001g0174 a0004c0004t0001g0205 others(2): Show |
5 | HG01981.hp2 HG03704.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.7047+572G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105651 | |||||||
chr18:13105731 | T | G | 1 | a0002c0001t0001g0332 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7047+652T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105731 | |||||||
chr18:13105851 | T | C | 3 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0035c0028t0001g0356 |
3 | HG01515.hp1 HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.7047+772T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13105851 | |||||||
chr18:13106256 | C | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+1177C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106256 | |||||||
chr18:13106257 | G | A | 1 | a0028c0043t0001g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7047+1178G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106257 | |||||||
chr18:13106338 | T | C | 292 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(289): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.7047+1259T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106338 | |||||||
chr18:13106374 | GCTACCAC others(82): Show |
G | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1308_7047+139 others(93): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106374 | ||||||
chr18:13106403 | CACTCACC others(73): Show |
C | 1 | a0001c0044t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7047+1350_7047+142 others(84): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106403 | ||||||
chr18:13106428 | CCACACAA others(8): Show |
C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1350_7047+136 others(19): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106428 | |||||||
chr18:13106447 | A | C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1368A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106447 | |||||||
chr18:13106452 | CACCCCAC others(2): Show |
C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1375_7047+138 others(13): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106452 | ||||||
chr18:13106462 | A | C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1383A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106462 | |||||||
chr18:13106465 | T | C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1386T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106465 | |||||||
chr18:13106477 | TACCACTA others(49): Show |
T | 66 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.7047+1402_7047+145 others(60): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106477 | ||||||
chr18:13106480 | C | T | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1401C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106480 | |||||||
chr18:13106483 | T | C | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7047+1404T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106483 | |||||||
chr18:13106509 | T | TACC | 5 | a0009c0009t0001g0219 a0014c0012t0001g0012 a0014c0012t0001g0113 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.7047+1455_7047+145 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106509 | ||||||
chr18:13106509 | T | TACCACCA others(8): Show |
6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7047+1443_7047+145 others(19): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13106509 | ||||||
chr18:13106519 | A | G | 2 | a0004c0004t0001g0002 a0004c0004t0001g0195 |
5 | NA18942.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.7047+1440A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106519 | |||||||
chr18:13106533 | C | T | 7 | a0001c0002t0001g0209 a0001c0002t0001g0211 a0001c0002t0001g0212 others(4): Show |
7 | HG01109.hp2 HG02132.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.7047+1454C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106533 | |||||||
chr18:13106834 | A | T | 1 | a0002c0001t0001g0328 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.7047+1755A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106834 | |||||||
chr18:13106996 | T | A | 5 | a0005c0005t0001g0014 a0005c0005t0001g0125 a0015c0014t0001g0013 others(2): Show |
6 | HG02132.hp1 NA18944.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.7047+1917T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13106996 | |||||||
chr18:13107181 | C | G | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7047+2102C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107181 | |||||||
chr18:13107231 | G | A | 2 | a0001c0002t0001g0230 a0010c0010t0002g0078 |
2 | HG01928.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.7047+2152G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107231 | |||||||
chr18:13107255 | A | C | 18 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(15): Show |
18 | HG01167.hp1 HG01884.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.7047+2176A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107255 | |||||||
chr18:13107337 | T | A | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7047+2258T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107337 | |||||||
chr18:13107434 | GA | G | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7047+2358delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107434 | ||||||
chr18:13107518 | A | G | 1 | a0005c0005t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7047+2439A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107518 | |||||||
chr18:13107560 | A | G | 2 | a0003c0003t0002g0076 a0003c0003t0002g0102 |
2 | HG00140.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.7047+2481A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107560 | |||||||
chr18:13107571 | G | A | 1 | a0034c0032t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.7047+2492G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107571 | |||||||
chr18:13107760 | C | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+2681C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107760 | |||||||
chr18:13107795 | A | G | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7047+2716A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107795 | |||||||
chr18:13107858 | C | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+2779C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107858 | |||||||
chr18:13107859 | G | A | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7047+2780G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107859 | |||||||
chr18:13107883 | C | A | 1 | a0007c0007t0002g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7047+2804C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107883 | |||||||
chr18:13107883 | C | CA | 14 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(11): Show |
14 | HG01167.hp1 HG01515.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.7047+2820dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | ||||||
chr18:13107883 | CA | C | 163 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(160): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.7047+2820delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | ||||||
chr18:13107883 | CAA | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.7047+2819_7047+282 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13107883 | ||||||
chr18:13107977 | G | C | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7047+2898G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13107977 | |||||||
chr18:13108021 | A | G | 1 | a0002c0001t0001g0344 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7047+2942A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108021 | |||||||
chr18:13108313 | TTAAAC | T | 4 | a0002c0001t0001g0340 a0002c0001t0001g0341 a0002c0001t0001g0359 others(1): Show |
4 | HG02976.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3239_7047+324 others(9): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13108313 | ||||||
chr18:13108375 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3296A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108375 | |||||||
chr18:13108524 | C | T | 9 | a0006c0006t0002g0026 a0007c0007t0002g0006 a0007c0007t0002g0007 others(6): Show |
11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7047+3445C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108524 | |||||||
chr18:13108538 | A | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3459A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108538 | |||||||
chr18:13108544 | C | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3465C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108544 | |||||||
chr18:13108594 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7047+3515G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108594 | |||||||
chr18:13108766 | T | C | 1 | a0003c0003t0002g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7047+3687T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108766 | |||||||
chr18:13108909 | A | T | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7047+3830A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108909 | |||||||
chr18:13108916 | C | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7047+3837C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13108916 | |||||||
chr18:13109170 | G | A | 77 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(74): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7047+4091G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109170 | |||||||
chr18:13109219 | T | C | 36 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(33): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.7047+4140T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109219 | |||||||
chr18:13109280 | A | G | 42 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(39): Show |
52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7047+4201A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109280 | |||||||
chr18:13109481 | C | T | 9 | a0006c0006t0002g0026 a0007c0007t0002g0006 a0007c0007t0002g0007 others(6): Show |
11 | HG01952.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.7048-4105C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109481 | |||||||
chr18:13109546 | A | C | 1 | a0002c0001t0001g0330 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7048-4040A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109546 | |||||||
chr18:13109556 | A | G | 137 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(134): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.7048-4030A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109556 | |||||||
chr18:13109649 | G | A | 2 | a0011c0011t0001g0282 a0011c0011t0001g0283 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.7048-3937G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109649 | |||||||
chr18:13109756 | AG | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3829delG | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109756 | |||||||
chr18:13109836 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7048-3750C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109836 | |||||||
chr18:13109880 | T | C | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7048-3706T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109880 | |||||||
chr18:13109977 | G | A | 2 | a0001c0002t0001g0256 a0001c0002t0001g0258 |
2 | NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.7048-3609G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109977 | |||||||
chr18:13109986 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3600G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13109986 | |||||||
chr18:13110149 | C | G | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7048-3437C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110149 | |||||||
chr18:13110272 | C | T | 42 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(39): Show |
52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7048-3314C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110272 | |||||||
chr18:13110431 | A | AT | 5 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(2): Show |
8 | HG00621.hp2 NA18522.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-3141dupT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13110431 | ||||||
chr18:13110431 | AT | A | 98 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(95): Show |
101 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.7048-3141delT | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | INFO_REALIGN_3_PRIME | chr18 | 13110431 | ||||||
chr18:13110558 | G | A | 1 | a0005c0005t0001g0126 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7048-3028G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110558 | |||||||
chr18:13110584 | G | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7048-3002G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110584 | |||||||
chr18:13110659 | A | G | 1 | a0005c0005t0001g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7048-2927A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110659 | |||||||
chr18:13110847 | G | A | 1 | a0010c0010t0002g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.7048-2739G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110847 | |||||||
chr18:13110859 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-2727C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110859 | |||||||
chr18:13110987 | G | A | 1 | a0005c0005t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.7048-2599G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13110987 | |||||||
chr18:13111110 | C | T | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7048-2476C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111110 | |||||||
chr18:13111194 | G | A | 6 | a0011c0011t0001g0282 a0011c0011t0001g0283 a0011c0011t0001g0334 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.7048-2392G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111194 | |||||||
chr18:13111243 | G | A | 1 | a0007c0007t0002g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7048-2343G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111243 | |||||||
chr18:13111283 | C | T | 3 | a0004c0004t0001g0177 a0004c0004t0001g0178 a0004c0004t0004g0176 |
3 | HG00558.hp2 NA18974.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.7048-2303C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111283 | |||||||
chr18:13111405 | G | A | 6 | a0003c0003t0002g0054 a0003c0003t0002g0062 a0005c0005t0001g0121 others(3): Show |
6 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.7048-2181G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111405 | |||||||
chr18:13111420 | C | T | 1 | a0006c0006t0002g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7048-2166C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111420 | |||||||
chr18:13111752 | C | T | 1 | a0011c0011t0001g0335 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7048-1834C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111752 | |||||||
chr18:13111824 | A | T | 4 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(1): Show |
4 | HG03041.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7048-1762A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111824 | |||||||
chr18:13111834 | A | G | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1752A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111834 | |||||||
chr18:13111835 | G | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1751G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111835 | |||||||
chr18:13111836 | A | G | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-1750A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13111836 | |||||||
chr18:13112047 | G | A | 1 | a0004c0004t0001g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7048-1539G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112047 | |||||||
chr18:13112215 | G | A | 3 | a0005c0005t0001g0134 a0005c0005t0001g0135 a0005c0005t0001g0136 |
3 | HG00099.hp2 HG01099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7048-1371G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112215 | |||||||
chr18:13112240 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7048-1346G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112240 | |||||||
chr18:13112411 | C | T | 1 | a0004c0004t0001g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.7048-1175C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112411 | |||||||
chr18:13112605 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7048-981T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112605 | |||||||
chr18:13112673 | T | C | 1 | a0005c0005t0001g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7048-913T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112673 | |||||||
chr18:13112680 | G | A | 3 | a0005c0005t0001g0150 a0019c0015t0002g0039 a0019c0015t0002g0040 |
3 | HG02895.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7048-906G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112680 | |||||||
chr18:13112884 | C | G | 1 | a0002c0001t0001g0325 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7048-702C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112884 | |||||||
chr18:13112982 | A | G | 1 | a0002c0001t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.7048-604A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112982 | |||||||
chr18:13112992 | T | C | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7048-594T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13112992 | |||||||
chr18:13113090 | T | C | 2 | a0006c0006t0002g0042 a0006c0006t0002g0043 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7048-496T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113090 | |||||||
chr18:13113095 | G | A | 1 | a0002c0001t0001g0305 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7048-491G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113095 | |||||||
chr18:13113111 | G | A | 1 | a0006c0006t0002g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7048-475G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113111 | |||||||
chr18:13113117 | C | G | 18 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(15): Show |
20 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.7048-469C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113117 | |||||||
chr18:13113134 | C | T | 1 | a0005c0005t0001g0156 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7048-452C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113134 | |||||||
chr18:13113153 | C | G | 1 | a0003c0003t0002g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7048-433C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113153 | |||||||
chr18:13113198 | C | T | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7048-388C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113198 | |||||||
chr18:13113209 | A | G | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7048-377A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113209 | |||||||
chr18:13113294 | T | C | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7048-292T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113294 | |||||||
chr18:13113447 | T | C | 3 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 |
6 | HG00621.hp2 NA18954.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.7048-139T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113447 | |||||||
chr18:13113462 | A | G | 1 | a0013c0029t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7048-124A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 40/44 | chr18 | 13113462 | |||||||
chr18:13113879 | C | T | 1 | a0006c0006t0002g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7167+174C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13113879 | |||||||
chr18:13113998 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7168-132T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13113998 | |||||||
chr18:13114026 | T | C | 2 | a0006c0006t0001g0355 a0006c0006t0001g0357 |
2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.7168-104T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114026 | |||||||
chr18:13114047 | A | ATG | 4 | a0001c0002t0001g0019 a0001c0002t0001g0266 a0001c0002t0001g0274 others(1): Show |
5 | HG01192.hp2 HG02004.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.7168-82_7168-81dup others(2): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chr18 | 13114047 | ||||||
chr18:13114047 | A | G | 42 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(39): Show |
52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.7168-83A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114047 | |||||||
chr18:13114053 | G | T | 1 | a0002c0001t0001g0021 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7168-77G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 41/44 | chr18 | 13114053 | |||||||
chr18:13114442 | T | C | 13 | a0005c0005t0001g0150 a0005c0005t0001g0152 a0005c0005t0001g0153 others(10): Show |
13 | HG01884.hp2 HG02717.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.7289+191T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13114442 | |||||||
chr18:13114715 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7289+464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13114715 | |||||||
chr18:13115011 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7289+760G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115011 | |||||||
chr18:13115021 | A | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7289+770A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115021 | |||||||
chr18:13115061 | A | G | 4 | a0003c0003t0002g0008 a0003c0003t0002g0057 a0003c0003t0002g0058 others(1): Show |
5 | HG00280.hp2 HG00741.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.7289+810A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115061 | |||||||
chr18:13115102 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7289+851A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115102 | |||||||
chr18:13115172 | A | G | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7289+921A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115172 | |||||||
chr18:13115264 | C | T | 1 | a0003c0003t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7289+1013C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115264 | |||||||
chr18:13115305 | C | T | 1 | a0003c0003t0002g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7289+1054C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115305 | |||||||
chr18:13115310 | T | C | 1 | a0005c0005t0001g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7289+1059T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115310 | |||||||
chr18:13115359 | G | A | 1 | a0005c0005t0001g0139 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.7290-1018G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115359 | |||||||
chr18:13115447 | C | T | 23 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(20): Show |
25 | HG01891.hp2 HG01952.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.7290-930C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115447 | |||||||
chr18:13115460 | T | C | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7290-917T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115460 | |||||||
chr18:13115461 | A | C | 1 | a0005c0005t0001g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7290-916A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115461 | |||||||
chr18:13115511 | C | T | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7290-866C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115511 | |||||||
chr18:13115520 | G | A | 3 | a0006c0006t0002g0041 a0006c0006t0002g0042 a0006c0006t0002g0043 |
3 | HG01891.hp2 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7290-857G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115520 | |||||||
chr18:13115693 | C | T | 1 | a0002c0001t0001g0330 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.7290-684C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115693 | |||||||
chr18:13115708 | A | G | 8 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(5): Show |
8 | HG01167.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.7290-669A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115708 | |||||||
chr18:13115750 | TCA | T | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7290-624_7290-623d others(4): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | INFO_REALIGN_3_PRIME | chr18 | 13115750 | ||||||
chr18:13115814 | G | T | 2 | a0002c0001t0001g0315 a0002c0001t0001g0316 |
2 | NA19060.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.7290-563G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115814 | |||||||
chr18:13115873 | A | G | 1 | a0002c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7290-504A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115873 | |||||||
chr18:13115917 | G | A | 1 | a0003c0003t0002g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7290-460G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115917 | |||||||
chr18:13115997 | T | C | 6 | a0006c0006t0001g0355 a0006c0006t0001g0357 a0013c0016t0003g0215 others(3): Show |
6 | HG01515.hp1 HG02258.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.7290-380T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13115997 | |||||||
chr18:13116002 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7290-375T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116002 | |||||||
chr18:13116013 | C | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7290-364C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116013 | |||||||
chr18:13116152 | C | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7290-225C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116152 | |||||||
chr18:13116236 | C | T | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7290-141C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116236 | |||||||
chr18:13116319 | A | G | 2 | a0005c0005t0001g0126 a0005c0005t0001g0139 |
2 | HG02015.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.7290-58A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116319 | |||||||
chr18:13116324 | T | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7290-53T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116324 | |||||||
chr18:13116359 | C | T | 16 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(13): Show |
18 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.7290-18C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 42/44 | chr18 | 13116359 | |||||||
chr18:13116597 | A | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7416+94A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116597 | |||||||
chr18:13116673 | G | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7416+170G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116673 | |||||||
chr18:13116710 | T | C | 4 | a0006c0006t0002g0034 a0006c0006t0002g0035 a0006c0006t0002g0037 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.7416+207T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116710 | |||||||
chr18:13116799 | C | T | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7416+296C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13116799 | |||||||
chr18:13117059 | C | CA | 87 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(84): Show |
93 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.7417-511dupA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chr18 | 13117059 | ||||||
chr18:13117246 | G | A | 72 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(69): Show |
75 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.7417-339G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117246 | |||||||
chr18:13117291 | C | T | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7417-294C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117291 | |||||||
chr18:13117348 | T | A | 3 | a0003c0003t0002g0011 a0003c0003t0002g0060 a0003c0003t0002g0085 |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.7417-237T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117348 | |||||||
chr18:13117372 | G | A | 2 | a0002c0001t0001g0287 a0002c0001t0001g0289 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7417-213G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117372 | |||||||
chr18:13117442 | T | C | 1 | a0006c0006t0002g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7417-143T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117442 | |||||||
chr18:13117540 | A | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7417-45A>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117540 | |||||||
chr18:13117568 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7417-17C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117568 | |||||||
chr18:13117570 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7417-15T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 43/44 | chr18 | 13117570 | |||||||
chr18:13117831 | G | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7475+188G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13117831 | |||||||
chr18:13118156 | G | A | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7475+513G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118156 | |||||||
chr18:13118179 | G | A | 1 | a0002c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7475+536G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118179 | |||||||
chr18:13118293 | GTCTC | G | 121 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(118): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.7475+653_7475+656d others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13118293 | ||||||
chr18:13118628 | A | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+985A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118628 | |||||||
chr18:13118648 | T | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1005T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118648 | |||||||
chr18:13118709 | A | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1066A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118709 | |||||||
chr18:13118764 | A | G | 3 | a0002c0001t0001g0305 a0002c0001t0001g0311 a0002c0001t0001g0313 |
3 | HG01361.hp1 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.7475+1121A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118764 | |||||||
chr18:13118787 | G | A | 4 | a0005c0005t0001g0121 a0005c0005t0001g0122 a0005c0005t0001g0123 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.7475+1144G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118787 | |||||||
chr18:13118796 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1153T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118796 | |||||||
chr18:13118798 | ACAT | A | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1174_7475+117 others(7): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13118798 | ||||||
chr18:13118807 | T | A | 1 | a0001c0002t0001g0273 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.7475+1164T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118807 | |||||||
chr18:13118819 | T | A | 2 | a0019c0015t0002g0039 a0019c0015t0002g0040 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7475+1176T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13118819 | |||||||
chr18:13119107 | A | G | 1 | a0003c0003t0002g0107 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.7475+1464A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119107 | |||||||
chr18:13119157 | A | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.7475+1514A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119157 | |||||||
chr18:13119307 | A | G | 1 | a0001c0002t0001g0249 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.7475+1664A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119307 | |||||||
chr18:13119337 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+1694T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119337 | |||||||
chr18:13119453 | A | T | 73 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(70): Show |
76 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.7475+1810A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119453 | |||||||
chr18:13119459 | T | C | 1 | a0001c0002t0001g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.7475+1816T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119459 | |||||||
chr18:13119614 | C | T | 41 | a0004c0004t0001g0001 a0004c0004t0001g0002 a0004c0004t0001g0005 others(38): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.7475+1971C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119614 | |||||||
chr18:13119658 | C | T | 1 | a0002c0001t0001g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7475+2015C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119658 | |||||||
chr18:13119730 | A | T | 1 | a0003c0003t0002g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7475+2087A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119730 | |||||||
chr18:13119744 | A | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+2101A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119744 | |||||||
chr18:13119745 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7475+2102T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119745 | |||||||
chr18:13119862 | C | T | 1 | a0002c0001t0001g0290 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7475+2219C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119862 | |||||||
chr18:13119899 | A | G | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7475+2256A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13119899 | |||||||
chr18:13120332 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+2689A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120332 | |||||||
chr18:13120384 | G | T | 114 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(111): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.7475+2741G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120384 | |||||||
chr18:13120417 | C | G | 1 | a0036c0035t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7475+2774C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120417 | |||||||
chr18:13120466 | G | T | 1 | a0003c0003t0002g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7475+2823G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120466 | |||||||
chr18:13120653 | G | C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+3010G>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120653 | |||||||
chr18:13120680 | G | A | 1 | a0002c0001t0001g0021 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7475+3037G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13120680 | |||||||
chr18:13121062 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7475+3419C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121062 | |||||||
chr18:13121151 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-3481G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121151 | |||||||
chr18:13121161 | T | C | 1 | a0001c0002t0001g0230 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7476-3471T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121161 | |||||||
chr18:13121221 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-3411T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121221 | |||||||
chr18:13121294 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7476-3338A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121294 | |||||||
chr18:13121432 | C | T | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-3200C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121432 | |||||||
chr18:13121626 | C | A | 1 | a0003c0003t0002g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.7476-3006C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121626 | |||||||
chr18:13121668 | C | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2964C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121668 | |||||||
chr18:13121681 | C | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2951C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121681 | |||||||
chr18:13121682 | T | C | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2950T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121682 | |||||||
chr18:13121683 | C | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2949C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121683 | |||||||
chr18:13121772 | A | G | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2860A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121772 | |||||||
chr18:13121802 | G | T | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7476-2830G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121802 | |||||||
chr18:13121805 | T | A | 1 | a0005c0005t0001g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.7476-2827T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121805 | |||||||
chr18:13121871 | C | T | 2 | a0002c0001t0001g0359 a0002c0001t0001g0360 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7476-2761C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121871 | |||||||
chr18:13121881 | T | C | 1 | a0003c0003t0002g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7476-2751T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121881 | |||||||
chr18:13121989 | C | T | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-2643C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13121989 | |||||||
chr18:13122017 | G | A | 1 | a0029c0020t0001g0354 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7476-2615G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122017 | |||||||
chr18:13122060 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-2572G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122060 | |||||||
chr18:13122151 | C | T | 1 | a0022c0021t0001g0346 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7476-2481C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122151 | |||||||
chr18:13122213 | A | G | 1 | a0009c0009t0001g0219 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7476-2419A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122213 | |||||||
chr18:13122355 | C | T | 1 | a0005c0005t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7476-2277C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122355 | |||||||
chr18:13122411 | A | T | 2 | a0013c0016t0003g0215 a0013c0016t0003g0216 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7476-2221A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122411 | |||||||
chr18:13122484 | G | A | 1 | a0007c0007t0002g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.7476-2148G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122484 | |||||||
chr18:13122529 | T | C | 1 | a0002c0001t0001g0309 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7476-2103T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122529 | |||||||
chr18:13122580 | GA | G | 282 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(279): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.7476-2041delA | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122580 | ||||||
chr18:13122619 | G | A | 20 | a0006c0006t0002g0026 a0006c0006t0002g0033 a0006c0006t0002g0034 others(17): Show |
22 | HG01891.hp2 HG01952.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.7476-2013G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122619 | |||||||
chr18:13122711 | T | G | 3 | a0013c0016t0003g0215 a0013c0016t0003g0216 a0013c0029t0003g0214 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.7476-1921T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122711 | |||||||
chr18:13122739 | C | T | 1 | a0005c0005t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7476-1893C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122739 | |||||||
chr18:13122760 | A | G | 4 | a0009c0009t0001g0003 a0009c0009t0001g0217 a0009c0009t0001g0218 others(1): Show |
7 | HG00621.hp2 NA18522.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.7476-1872A>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122760 | |||||||
chr18:13122832 | C | CGT | 6 | a0005c0005t0001g0123 a0005c0005t0001g0124 a0009c0009t0001g0003 others(3): Show |
9 | HG00621.hp2 HG01167.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.7476-1773_7476-177 others(6): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | ||||||
chr18:13122832 | C | CGTGT | 8 | a0008c0008t0001g0128 a0008c0008t0001g0129 a0008c0008t0001g0130 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.7476-1775_7476-177 others(8): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | ||||||
chr18:13122832 | CGTGTGT | C | 149 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(146): Show |
164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.7476-1777_7476-177 others(10): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | ||||||
chr18:13122832 | CGTGTGTG others(1): Show |
C | 102 | a0002c0001t0001g0020 a0002c0001t0001g0021 a0002c0001t0001g0022 others(99): Show |
108 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.7476-1779_7476-177 others(12): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | ||||||
chr18:13122832 | CGTGTGTG others(3): Show |
C | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-1781_7476-177 others(14): Show |
CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | INFO_REALIGN_3_PRIME | chr18 | 13122832 | ||||||
chr18:13122850 | T | A | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-1782T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122850 | |||||||
chr18:13122878 | T | C | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1754T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122878 | |||||||
chr18:13122881 | A | T | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1751A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122881 | |||||||
chr18:13122897 | G | T | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1735G>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122897 | |||||||
chr18:13122900 | C | G | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1732C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122900 | |||||||
chr18:13122901 | T | A | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1731T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122901 | |||||||
chr18:13122902 | T | G | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1730T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122902 | |||||||
chr18:13122903 | T | A | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1729T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122903 | |||||||
chr18:13122909 | A | T | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1723A>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122909 | |||||||
chr18:13122912 | T | A | 1 | a0004c0004t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.7476-1720T>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13122912 | |||||||
chr18:13123319 | C | A | 1 | a0005c0005t0001g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7476-1313C>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123319 | |||||||
chr18:13123319 | C | G | 8 | a0005c0005t0001g0152 a0005c0005t0001g0153 a0005c0005t0001g0154 others(5): Show |
8 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.7476-1313C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123319 | |||||||
chr18:13123556 | T | C | 1 | a0032c0037t0002g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.7476-1076T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123556 | |||||||
chr18:13123578 | C | T | 1 | a0005c0005t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7476-1054C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123578 | |||||||
chr18:13123591 | T | G | 1 | a0001c0034t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7476-1041T>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123591 | |||||||
chr18:13123632 | C | T | 3 | a0018c0019t0001g0165 a0018c0019t0001g0166 a0028c0043t0001g0164 |
3 | HG02559.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7476-1000C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123632 | |||||||
chr18:13123646 | C | G | 276 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(273): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.7476-986C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123646 | |||||||
chr18:13123876 | C | T | 9 | a0002c0001t0001g0336 a0002c0001t0001g0337 a0002c0001t0001g0338 others(6): Show |
9 | HG02976.hp1 HG03041.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.7476-756C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123876 | |||||||
chr18:13123877 | C | G | 288 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(285): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.7476-755C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123877 | |||||||
chr18:13123939 | C | T | 1 | a0001c0002t0001g0271 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7476-693C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13123939 | |||||||
chr18:13124043 | C | G | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.7476-589C>G | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124043 | |||||||
chr18:13124156 | G | A | 1 | a0005c0005t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7476-476G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124156 | |||||||
chr18:13124416 | C | T | 77 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(74): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7476-216C>T | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124416 | |||||||
chr18:13124447 | G | A | 4 | a0014c0012t0001g0012 a0014c0012t0001g0113 a0014c0012t0001g0114 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.7476-185G>A | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124447 | |||||||
chr18:13124610 | T | C | 68 | a0001c0002t0001g0017 a0001c0002t0001g0018 a0001c0002t0001g0019 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.7476-22T>C | CEP192 | ENSG00000101639.19 | transcript | ENST00000506447.5 | protein_coding | 44/44 | chr18 | 13124610 |