Item | Value |
---|---|
geneid | 11116 |
ensemblid | ENSG00000213066.14 |
hgncid | 17012 |
symbol | CEP43 |
name | centrosomal protein 43 |
refseq_nuc | NM_007045.4 |
refseq_prot | NP_008976.1 |
ensembl_nuc | ENST00000366847.9 |
ensembl_prot | ENSP00000355812.3 |
mane_status | MANE Select |
chr | chr6 |
start | 166999397 |
end | 167052718 |
strand | + |
ver | v1.2 |
region | chr6:166999397-167052718 |
region5000 | chr6:166994397-167057718 |
regionname0 | CEP43_chr6_166999397_167052718 |
regionname5000 | CEP43_chr6_166994397_167057718 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 399 | 335 | 63 | 59 | 162 | 16 | 33 | 128 | CEP43_chr6_166994397_167057718 | CEP43 | MAATA others(394): Show |
chr6 | 166994397 | 167057718 |
a0002 | 0/0 | 399 | 21 | 2 | 1 | 15 | 0 | 3 | 12 | CEP43_chr6_166994397_167057718 | CEP43 | MAATA others(394): Show |
chr6 | 166994397 | 167057718 |
a0003 | 0/0 | 399 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | MAATT others(394): Show |
chr6 | 166994397 | 167057718 |
a0004 | 0/0 | 399 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | MAATA others(394): Show |
chr6 | 166994397 | 167057718 |
a0005 | 0/0 | 399 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | MAATA others(394): Show |
chr6 | 166994397 | 167057718 |
a0006 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | MAATA others(394): Show |
chr6 | 166994397 | 167057718 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1197 | 334 | 63 | 59 | 162 | 16 | 33 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0001c0006 | 0/1 | 1197 | 1 | 0 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0002c0002 | 0/0 | 1197 | 21 | 2 | 1 | 15 | 0 | 3 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0003c0003 | 0/0 | 1197 | 8 | 7 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0004c0004 | 0/0 | 1197 | 6 | 5 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0005c0005 | 0/0 | 1197 | 5 | 5 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 | ||
a0006c0007 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | ATGGC others(1192): Show |
chr6 | 166994397 | 167057718 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13978 | 21 | 0 | 0 | 16 | 1 | 4 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0002 | 0/0 | 13968 | 18 | 4 | 3 | 9 | 0 | 2 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0003 | 0/0 | 13970 | 14 | 0 | 2 | 8 | 2 | 2 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0004 | 0/0 | 13978 | 9 | 0 | 0 | 9 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0005 | 0/0 | 13969 | 6 | 3 | 2 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0006 | 0/0 | 13964 | 6 | 0 | 2 | 2 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0007 | 0/0 | 13955 | 5 | 3 | 1 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13950): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0008 | 0/0 | 13969 | 5 | 0 | 0 | 5 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0010 | 0/0 | 13973 | 5 | 0 | 0 | 5 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0011 | 0/0 | 13976 | 5 | 0 | 4 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0012 | 0/0 | 13980 | 5 | 0 | 3 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0013 | 0/0 | 13976 | 5 | 0 | 0 | 2 | 1 | 2 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0014 | 0/0 | 13974 | 5 | 0 | 1 | 4 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0016 | 0/0 | 13982 | 4 | 0 | 0 | 4 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0017 | 0/0 | 13967 | 4 | 1 | 0 | 2 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13962): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0018 | 1/0 | 13956 | 3 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13951): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0020 | 0/0 | 13974 | 3 | 2 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0021 | 0/0 | 13978 | 3 | 0 | 0 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0022 | 0/0 | 13972 | 3 | 0 | 3 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0023 | 0/0 | 13968 | 3 | 0 | 0 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0024 | 0/0 | 13966 | 3 | 0 | 1 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13961): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0025 | 0/0 | 13968 | 3 | 0 | 0 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0026 | 0/0 | 13975 | 2 | 1 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0027 | 0/0 | 13957 | 2 | 0 | 0 | 0 | 1 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13952): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0028 | 0/0 | 13961 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13956): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0029 | 0/0 | 13950 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13945): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0030 | 0/0 | 13975 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0031 | 0/0 | 13973 | 2 | 0 | 0 | 1 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0032 | 0/0 | 13975 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0033 | 0/0 | 13973 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0034 | 0/0 | 13973 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0037 | 0/0 | 13980 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0039 | 0/0 | 13976 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0040 | 0/0 | 13976 | 2 | 1 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0041 | 0/0 | 13973 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0042 | 0/0 | 13956 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13951): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0043 | 0/0 | 13981 | 2 | 0 | 0 | 0 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0044 | 0/0 | 13978 | 2 | 0 | 0 | 0 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0045 | 0/0 | 13973 | 2 | 0 | 1 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0046 | 0/0 | 13969 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0047 | 0/0 | 13958 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13953): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0048 | 0/0 | 13982 | 2 | 0 | 1 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0049 | 0/0 | 13982 | 2 | 0 | 1 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0050 | 0/0 | 13980 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0051 | 0/0 | 13976 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0052 | 0/0 | 13974 | 2 | 0 | 1 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0053 | 0/0 | 13970 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0054 | 0/0 | 13992 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13987): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0055 | 0/0 | 13976 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0056 | 0/0 | 13979 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0057 | 0/0 | 13976 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0058 | 0/0 | 13975 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0059 | 0/0 | 13972 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0060 | 0/0 | 13961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13956): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0061 | 0/0 | 13955 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13950): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0062 | 0/0 | 13957 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13952): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0063 | 0/0 | 13963 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13958): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0064 | 0/0 | 13962 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13957): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0065 | 0/0 | 13961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13956): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0066 | 0/0 | 13961 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13956): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0067 | 0/0 | 13962 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13957): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0068 | 0/0 | 13975 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0069 | 0/0 | 13973 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0070 | 0/0 | 13971 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0071 | 0/0 | 13969 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0072 | 0/0 | 13969 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0073 | 0/0 | 13965 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0075 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0076 | 0/0 | 13974 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0077 | 0/0 | 13969 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0078 | 0/0 | 13969 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0079 | 0/0 | 13970 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0080 | 0/0 | 13973 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0084 | 0/0 | 13950 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13945): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0085 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0086 | 0/0 | 13973 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0087 | 0/0 | 13975 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0089 | 0/0 | 13978 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0104 | 0/0 | 13972 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0105 | 0/0 | 13980 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0106 | 0/0 | 13978 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0107 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13979): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0108 | 0/0 | 13980 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0110 | 0/0 | 13978 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0112 | 0/0 | 13976 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0113 | 0/0 | 13975 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0115 | 0/0 | 13974 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0116 | 0/0 | 13976 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0117 | 0/0 | 13972 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0118 | 0/0 | 13970 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0119 | 0/0 | 13970 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0120 | 0/0 | 13970 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0121 | 0/0 | 13964 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0122 | 0/0 | 13973 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0123 | 0/0 | 13969 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0124 | 0/0 | 13972 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0125 | 0/0 | 13971 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0126 | 0/0 | 13968 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0127 | 0/0 | 13976 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0128 | 0/0 | 13975 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0129 | 0/0 | 13975 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0130 | 0/0 | 13974 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0131 | 0/0 | 13972 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0132 | 0/0 | 13970 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0133 | 0/0 | 13982 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0134 | 0/0 | 13983 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13978): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0135 | 0/0 | 13980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0136 | 0/0 | 13983 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13978): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0137 | 0/0 | 13979 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0138 | 0/0 | 13979 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0139 | 0/0 | 13979 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0140 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0141 | 0/0 | 13977 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13972): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0142 | 0/0 | 13974 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0143 | 0/0 | 13975 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0144 | 0/0 | 13980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0145 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0146 | 0/0 | 13973 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0147 | 0/0 | 13992 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13987): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0148 | 0/0 | 13980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0149 | 0/0 | 13975 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0150 | 0/0 | 13977 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13972): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0151 | 0/0 | 13974 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0152 | 0/0 | 13971 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0153 | 0/0 | 13975 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0154 | 0/0 | 13974 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13969): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0155 | 0/0 | 13987 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13982): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0156 | 0/0 | 13971 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0157 | 0/0 | 13971 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0158 | 0/0 | 13975 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0159 | 0/0 | 13970 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0160 | 0/0 | 13973 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0161 | 0/0 | 13967 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13962): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0162 | 0/0 | 13967 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13962): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0163 | 0/0 | 13970 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0164 | 0/0 | 13968 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0165 | 0/0 | 13973 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13968): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0166 | 0/0 | 13968 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0167 | 0/0 | 13968 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0168 | 0/0 | 13968 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0169 | 0/0 | 13970 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0170 | 0/0 | 13969 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0171 | 0/0 | 13968 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0172 | 0/0 | 13963 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13958): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0173 | 0/0 | 13965 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0174 | 0/0 | 13965 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0175 | 0/0 | 13964 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0176 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0177 | 0/0 | 13970 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13965): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0178 | 0/0 | 13964 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0179 | 0/0 | 13972 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0180 | 0/0 | 13978 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0181 | 0/0 | 13981 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0182 | 0/0 | 13992 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13987): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0183 | 0/0 | 13988 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13983): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0184 | 0/0 | 13986 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13981): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0185 | 0/0 | 13984 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13979): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0186 | 0/0 | 13984 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13979): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0187 | 0/0 | 13980 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0188 | 0/0 | 13981 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0189 | 0/0 | 13978 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0190 | 0/0 | 13978 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0191 | 0/0 | 13977 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13972): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0192 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0193 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0194 | 0/0 | 13972 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13967): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0195 | 0/0 | 13971 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13966): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0196 | 0/0 | 13987 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13982): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0197 | 0/0 | 13993 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13988): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0198 | 0/0 | 13984 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13979): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0199 | 0/0 | 13982 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0200 | 0/0 | 13981 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0201 | 0/0 | 13980 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0202 | 0/0 | 13979 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0203 | 0/0 | 13979 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0204 | 0/0 | 13978 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0205 | 0/0 | 13979 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0206 | 0/0 | 13976 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0207 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0208 | 0/0 | 13975 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0209 | 0/0 | 13966 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13961): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0210 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0211 | 0/0 | 13981 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0212 | 0/0 | 13980 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13975): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0213 | 0/0 | 13979 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13974): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0214 | 0/0 | 13976 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0215 | 0/0 | 13978 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0216 | 0/0 | 13978 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0001c0001t0217 | 0/0 | 13982 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13977): Show |
chr6 | 166994397 | 167057718 |
a0001c0006t0047 | 0/1 | 13958 | 1 | 0 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13953): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0015 | 0/0 | 13963 | 4 | 0 | 0 | 4 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13958): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0035 | 0/0 | 13967 | 2 | 0 | 1 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13962): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0036 | 0/0 | 13965 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0091 | 0/0 | 13968 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0092 | 0/0 | 13965 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0093 | 0/0 | 13968 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13963): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0094 | 0/0 | 13964 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0095 | 0/0 | 13963 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13958): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0096 | 0/0 | 13966 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13961): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0097 | 0/0 | 13965 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13960): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0098 | 0/0 | 13958 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13953): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0099 | 0/0 | 13957 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13952): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0100 | 0/0 | 13963 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13958): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0101 | 0/0 | 13964 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13959): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0102 | 0/0 | 13966 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13961): Show |
chr6 | 166994397 | 167057718 |
a0002c0002t0103 | 0/0 | 13966 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13961): Show |
chr6 | 166994397 | 167057718 |
a0003c0003t0009 | 0/0 | 13957 | 5 | 5 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13952): Show |
chr6 | 166994397 | 167057718 |
a0003c0003t0081 | 0/0 | 13956 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13951): Show |
chr6 | 166994397 | 167057718 |
a0003c0003t0082 | 0/0 | 13959 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13954): Show |
chr6 | 166994397 | 167057718 |
a0003c0003t0083 | 0/0 | 13958 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13953): Show |
chr6 | 166994397 | 167057718 |
a0004c0004t0038 | 0/0 | 13978 | 2 | 1 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0004c0004t0039 | 0/0 | 13976 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13971): Show |
chr6 | 166994397 | 167057718 |
a0004c0004t0109 | 0/0 | 13981 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13976): Show |
chr6 | 166994397 | 167057718 |
a0004c0004t0111 | 0/0 | 13978 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13973): Show |
chr6 | 166994397 | 167057718 |
a0004c0004t0114 | 0/0 | 13975 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13970): Show |
chr6 | 166994397 | 167057718 |
a0005c0005t0019 | 0/0 | 13969 | 3 | 3 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13964): Show |
chr6 | 166994397 | 167057718 |
a0005c0005t0074 | 0/0 | 13977 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13972): Show |
chr6 | 166994397 | 167057718 |
a0005c0005t0088 | 0/0 | 13967 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13962): Show |
chr6 | 166994397 | 167057718 |
a0006c0007t0090 | 0/0 | 13959 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | GTCTT others(13954): Show |
chr6 | 166994397 | 167057718 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0008g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0008g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0010g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0011g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0011g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0011g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0012g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0013g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0014g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0014g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0016g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0017g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0017g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0017g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0018g0009 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0020g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0020g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0021g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0021g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0022g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0022g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0023g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0023g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0023g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0024g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0024g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0024g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0025g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0025g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0026g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0026g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0027g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0028g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0028g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0029g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0029g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0030g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0030g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0031g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0031g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0032g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0033g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0033g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0034g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0037g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0037g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0039g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0040g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0040g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0041g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0041g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0042g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0042g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0043g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0044g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0045g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0045g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0046g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0046g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0047g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0048g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0049g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0049g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0050g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0050g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0051g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0052g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0052g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0053g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0054g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0055g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0056g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0056g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0057g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0057g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0058g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0059g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0059g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0060g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0061g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0062g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0063g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0064g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0065g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0066g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0067g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0068g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0069g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0070g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0071g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0072g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0073g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0075g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0076g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0077g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0078g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0079g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0080g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0084g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0085g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0086g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0087g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0089g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0104g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0105g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0106g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0107g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0108g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0110g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0112g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0113g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0115g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0116g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0117g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0118g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0119g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0120g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0121g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0122g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0123g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0124g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0125g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0126g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0127g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0128g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0129g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0130g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0131g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0132g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0133g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0134g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0135g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0136g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0137g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0138g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0139g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0140g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0141g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0142g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0143g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0144g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0145g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0146g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0147g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0148g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0149g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0150g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0151g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0152g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0153g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0154g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0155g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0156g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0157g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0158g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0159g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0160g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0161g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0162g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0163g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0164g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0165g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0166g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0167g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0168g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0169g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0170g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0171g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0172g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0173g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0174g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0175g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0176g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0177g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0178g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0179g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0180g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0181g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0182g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0183g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0184g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0185g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0186g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0187g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0188g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0189g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0190g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0191g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0192g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0193g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0194g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0195g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0196g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0197g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0198g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0199g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0200g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0201g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0202g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0203g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0204g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0205g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0206g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0207g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0208g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0209g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0210g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0211g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0212g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0213g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0214g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0215g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0216g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0001t0217g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0001c0006t0047g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0015g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0035g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0035g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0036g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0036g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0091g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0092g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0093g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0094g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0095g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0096g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0097g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0098g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0099g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0100g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0101g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0102g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0002c0002t0103g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0081g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0082g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0003c0003t0083g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0038g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0038g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0039g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0109g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0111g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0004c0004t0114g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0005c0005t0019g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0005c0005t0019g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0005c0005t0074g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0005c0005t0088g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
a0006c0007t0090g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0044 | g0032 | EUR | GBR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00099 | hp2 | a0001 | c0001 | t0027 | g0018 | EUR | GBR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0219 | EUR | GBR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00140 | hp2 | a0001 | c0001 | t0152 | g0043 | EUR | GBR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00280 | hp1 | a0001 | c0001 | t0062 | g0018 | EUR | FIN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0044 | EUR | FIN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00323 | hp2 | a0001 | c0001 | t0153 | g0007 | EUR | FIN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00408 | hp1 | a0001 | c0001 | t0010 | g0188 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00544 | hp1 | a0001 | c0001 | t0196 | g0118 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00544 | hp2 | a0001 | c0001 | t0135 | g0078 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00597 | hp1 | a0001 | c0001 | t0031 | g0185 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00597 | hp2 | a0006 | c0007 | t0090 | g0194 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00609 | hp1 | a0002 | c0002 | t0015 | g0010 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00621 | hp1 | a0001 | c0001 | t0030 | g0033 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00621 | hp2 | a0002 | c0002 | t0102 | g0040 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00639 | hp1 | a0001 | c0001 | t0174 | g0231 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00639 | hp2 | a0001 | c0001 | t0014 | g0001 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00642 | hp2 | a0004 | c0004 | t0038 | g0089 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00673 | hp1 | a0001 | c0001 | t0216 | g0144 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00735 | hp1 | a0001 | c0001 | t0212 | g0028 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00735 | hp2 | a0001 | c0001 | t0194 | g0146 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00738 | hp1 | a0001 | c0001 | t0182 | g0004 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00741 | hp1 | a0001 | c0001 | t0150 | g0242 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG00741 | hp2 | a0001 | c0001 | t0200 | g0128 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01069 | hp1 | a0001 | c0001 | t0187 | g0156 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0029 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01071 | hp1 | a0001 | c0001 | t0012 | g0029 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01071 | hp2 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01074 | hp2 | a0001 | c0001 | t0048 | g0004 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01099 | hp1 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01099 | hp2 | a0001 | c0001 | t0110 | g0161 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0260 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0252 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01109 | hp1 | a0003 | c0003 | t0082 | g0036 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01109 | hp2 | a0001 | c0001 | t0154 | g0007 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01168 | hp1 | a0001 | c0001 | t0011 | g0132 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01168 | hp2 | a0001 | c0001 | t0173 | g0272 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01175 | hp1 | a0001 | c0001 | t0197 | g0143 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0224 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01192 | hp1 | a0001 | c0001 | t0022 | g0007 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01192 | hp2 | a0001 | c0001 | t0133 | g0004 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01243 | hp1 | a0001 | c0001 | t0127 | g0052 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01243 | hp2 | a0001 | c0001 | t0040 | g0025 | AMR | PUR | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01255 | hp1 | a0001 | c0001 | t0049 | g0154 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01255 | hp2 | a0001 | c0001 | t0024 | g0011 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01256 | hp1 | a0001 | c0001 | t0162 | g0228 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01256 | hp2 | a0001 | c0001 | t0011 | g0031 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01257 | hp1 | a0001 | c0001 | t0054 | g0027 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01257 | hp2 | a0001 | c0001 | t0188 | g0150 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01261 | hp1 | a0001 | c0001 | t0045 | g0247 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01261 | hp2 | a0001 | c0001 | t0147 | g0245 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01346 | hp2 | a0001 | c0001 | t0053 | g0017 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01358 | hp1 | a0001 | c0001 | t0189 | g0125 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01358 | hp2 | a0001 | c0001 | t0054 | g0027 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01361 | hp1 | a0002 | c0002 | t0035 | g0200 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01496 | hp1 | a0001 | c0001 | t0022 | g0249 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01496 | hp2 | a0001 | c0001 | t0022 | g0007 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01515 | hp1 | a0001 | c0001 | t0017 | g0011 | EUR | IBS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01515 | hp2 | a0001 | c0001 | t0043 | g0030 | EUR | IBS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0044 | EUR | IBS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01517 | hp2 | a0001 | c0001 | t0043 | g0030 | EUR | IBS | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01884 | hp1 | a0001 | c0001 | t0065 | g0165 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01884 | hp2 | a0001 | c0001 | t0117 | g0065 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01891 | hp1 | a0001 | c0001 | t0132 | g0159 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01891 | hp2 | a0001 | c0001 | t0050 | g0104 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01928 | hp1 | a0001 | c0001 | t0198 | g0015 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01934 | hp1 | a0001 | c0001 | t0195 | g0001 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01934 | hp2 | a0001 | c0001 | t0199 | g0015 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01978 | hp1 | a0001 | c0001 | t0206 | g0015 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01978 | hp2 | a0001 | c0001 | t0011 | g0008 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01993 | hp1 | a0001 | c0001 | t0183 | g0142 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01993 | hp2 | a0001 | c0001 | t0155 | g0248 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02004 | hp1 | a0001 | c0001 | t0211 | g0138 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0123 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02027 | hp2 | a0001 | c0001 | t0033 | g0181 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02040 | hp1 | a0001 | c0001 | t0017 | g0211 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02040 | hp2 | a0001 | c0001 | t0167 | g0256 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02074 | hp1 | a0001 | c0001 | t0059 | g0102 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02074 | hp2 | a0001 | c0001 | t0030 | g0187 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02080 | hp1 | a0001 | c0001 | t0052 | g0008 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02080 | hp2 | a0002 | c0002 | t0096 | g0199 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02083 | hp1 | a0001 | c0001 | t0017 | g0261 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02129 | hp1 | a0001 | c0001 | t0023 | g0263 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02132 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02132 | hp2 | a0001 | c0001 | t0142 | g0012 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02135 | hp1 | a0001 | c0001 | t0024 | g0215 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02135 | hp2 | a0001 | c0001 | t0143 | g0088 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02145 | hp1 | a0004 | c0004 | t0114 | g0164 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02145 | hp2 | a0002 | c0002 | t0092 | g0197 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02155 | hp1 | a0001 | c0001 | t0214 | g0001 | EAS | CDX | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02155 | hp2 | a0001 | c0001 | t0140 | g0082 | EAS | CDX | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02257 | hp1 | a0001 | c0001 | t0050 | g0129 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02257 | hp2 | a0004 | c0004 | t0038 | g0098 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02258 | hp1 | a0001 | c0001 | t0115 | g0025 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02258 | hp2 | a0001 | c0001 | t0029 | g0276 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02280 | hp2 | a0003 | c0003 | t0081 | g0036 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02293 | hp1 | a0001 | c0001 | t0053 | g0017 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02293 | hp2 | a0001 | c0001 | t0169 | g0271 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02300 | hp1 | a0001 | c0001 | t0052 | g0026 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02300 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PEL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02451 | hp1 | a0001 | c0001 | t0041 | g0051 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02451 | hp2 | a0001 | c0001 | t0060 | g0076 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02523 | hp1 | a0001 | c0001 | t0137 | g0022 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02523 | hp2 | a0001 | c0001 | t0178 | g0006 | EAS | KHV | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02572 | hp1 | a0005 | c0005 | t0019 | g0209 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02572 | hp2 | a0001 | c0001 | t0131 | g0071 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02615 | hp1 | a0001 | c0001 | t0070 | g0173 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02615 | hp2 | a0001 | c0001 | t0020 | g0063 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02622 | hp1 | a0001 | c0001 | t0067 | g0167 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02622 | hp2 | a0003 | c0003 | t0083 | g0190 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02630 | hp1 | a0001 | c0001 | t0063 | g0077 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02647 | hp2 | a0001 | c0001 | t0066 | g0166 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02698 | hp2 | a0001 | c0001 | t0020 | g0056 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02717 | hp1 | a0001 | c0001 | t0041 | g0175 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02717 | hp2 | a0001 | c0001 | t0061 | g0066 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02735 | hp1 | a0001 | c0001 | t0215 | g0152 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0170 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02738 | hp1 | a0001 | c0001 | t0125 | g0060 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02738 | hp2 | a0001 | c0001 | t0149 | g0213 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02809 | hp1 | a0001 | c0001 | t0026 | g0157 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02809 | hp2 | a0001 | c0001 | t0084 | g0275 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02818 | hp1 | a0001 | c0001 | t0108 | g0094 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02886 | hp1 | a0001 | c0001 | t0116 | g0068 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02886 | hp2 | a0001 | c0001 | t0118 | g0072 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02895 | hp1 | a0003 | c0003 | t0009 | g0037 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02895 | hp2 | a0005 | c0005 | t0088 | g0210 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02896 | hp1 | a0001 | c0001 | t0051 | g0149 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02896 | hp2 | a0001 | c0001 | t0017 | g0011 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02897 | hp1 | a0001 | c0001 | t0051 | g0134 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02897 | hp2 | a0003 | c0003 | t0009 | g0037 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02922 | hp1 | a0001 | c0001 | t0104 | g0058 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02922 | hp2 | a0001 | c0001 | t0073 | g0191 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02965 | hp1 | a0003 | c0003 | t0009 | g0038 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02965 | hp2 | a0004 | c0004 | t0109 | g0023 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02970 | hp1 | a0001 | c0001 | t0068 | g0172 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02970 | hp2 | a0001 | c0001 | t0042 | g0062 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03041 | hp1 | a0001 | c0001 | t0029 | g0274 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03041 | hp2 | a0001 | c0001 | t0039 | g0064 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03098 | hp1 | a0001 | c0001 | t0181 | g0121 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03098 | hp2 | a0003 | c0003 | t0009 | g0038 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03130 | hp1 | a0001 | c0001 | t0171 | g0216 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03130 | hp2 | a0001 | c0001 | t0107 | g0155 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03195 | hp1 | a0001 | c0001 | t0042 | g0061 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03195 | hp2 | a0001 | c0001 | t0028 | g0075 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03209 | hp1 | a0003 | c0003 | t0009 | g0189 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03209 | hp2 | a0001 | c0001 | t0120 | g0073 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03225 | hp1 | a0001 | c0001 | t0072 | g0193 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03225 | hp2 | a0001 | c0001 | t0069 | g0174 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03486 | hp1 | a0005 | c0005 | t0019 | g0041 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03486 | hp2 | a0002 | c0002 | t0103 | g0195 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03490 | hp1 | a0001 | c0001 | t0184 | g0004 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03490 | hp2 | a0001 | c0001 | t0126 | g0055 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03516 | hp1 | a0004 | c0004 | t0039 | g0093 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03516 | hp2 | a0001 | c0001 | t0064 | g0168 | AFR | ESN | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03540 | hp2 | a0001 | c0001 | t0040 | g0024 | AFR | GWD | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03579 | hp1 | a0001 | c0001 | t0128 | g0162 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03579 | hp2 | a0001 | c0001 | t0112 | g0024 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03654 | hp2 | a0001 | c0001 | t0217 | g0004 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03688 | hp1 | a0001 | c0001 | t0185 | g0135 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03688 | hp2 | a0001 | c0001 | t0106 | g0086 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03704 | hp2 | a0001 | c0001 | t0123 | g0070 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03710 | hp1 | a0001 | c0001 | t0027 | g0018 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03831 | hp1 | a0001 | c0001 | t0048 | g0004 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03831 | hp2 | a0001 | c0001 | t0146 | g0087 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03834 | hp1 | a0001 | c0001 | t0180 | g0153 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03834 | hp2 | a0001 | c0001 | t0105 | g0091 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03927 | hp1 | a0001 | c0001 | t0213 | g0114 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03942 | hp1 | a0002 | c0002 | t0097 | g0204 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03942 | hp2 | a0001 | c0001 | t0013 | g0101 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04184 | hp1 | a0001 | c0001 | t0013 | g0112 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04184 | hp2 | a0001 | c0001 | t0113 | g0057 | SAS | BEB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04199 | hp2 | a0001 | c0001 | t0049 | g0107 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04204 | hp1 | a0002 | c0002 | t0100 | g0196 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04204 | hp2 | a0001 | c0001 | t0202 | g0110 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04228 | hp1 | a0001 | c0001 | t0031 | g0002 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG04228 | hp2 | a0001 | c0001 | t0124 | g0059 | SAS | STU | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18522 | hp1 | a0001 | c0001 | t0186 | g0001 | AFR | YRI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | YRI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18612 | hp2 | a0001 | c0001 | t0034 | g0002 | EAS | CHB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18747 | hp1 | a0001 | c0001 | t0016 | g0083 | EAS | CHB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18747 | hp2 | a0001 | c0001 | t0086 | g0180 | EAS | CHB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18906 | hp1 | a0005 | c0005 | t0074 | g0208 | AFR | YRI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18906 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | YRI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18940 | hp1 | a0001 | c0001 | t0151 | g0270 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18940 | hp2 | a0001 | c0001 | t0057 | g0108 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18941 | hp1 | a0001 | c0001 | t0037 | g0130 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18941 | hp2 | a0001 | c0001 | t0148 | g0006 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18942 | hp1 | a0001 | c0001 | t0037 | g0136 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18942 | hp2 | a0001 | c0001 | t0161 | g0229 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18945 | hp1 | a0001 | c0001 | t0134 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18945 | hp2 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18946 | hp1 | a0001 | c0001 | t0192 | g0133 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18946 | hp2 | a0001 | c0001 | t0055 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18947 | hp1 | a0001 | c0001 | t0190 | g0131 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18947 | hp2 | a0001 | c0001 | t0163 | g0020 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18948 | hp1 | a0002 | c0002 | t0095 | g0198 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18949 | hp1 | a0001 | c0001 | t0179 | g0269 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18949 | hp2 | a0001 | c0001 | t0191 | g0113 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18950 | hp1 | a0002 | c0002 | t0036 | g0202 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18950 | hp2 | a0001 | c0001 | t0025 | g0239 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18951 | hp1 | a0001 | c0001 | t0136 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18952 | hp1 | a0001 | c0001 | t0025 | g0250 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18952 | hp2 | a0001 | c0001 | t0204 | g0085 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18953 | hp1 | a0001 | c0001 | t0076 | g0179 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18953 | hp2 | a0001 | c0001 | t0013 | g0137 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18954 | hp1 | a0001 | c0001 | t0016 | g0096 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18957 | hp1 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18959 | hp1 | a0001 | c0001 | t0056 | g0117 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18963 | hp1 | a0001 | c0001 | t0058 | g0001 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18963 | hp2 | a0002 | c0002 | t0015 | g0206 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18966 | hp1 | a0001 | c0001 | t0144 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18966 | hp2 | a0001 | c0001 | t0011 | g0031 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18970 | hp2 | a0002 | c0002 | t0036 | g0010 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18972 | hp1 | a0001 | c0001 | t0193 | g0008 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18972 | hp2 | a0001 | c0001 | t0168 | g0240 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18973 | hp1 | a0001 | c0001 | t0177 | g0268 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18975 | hp1 | a0001 | c0001 | t0157 | g0243 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18975 | hp2 | a0001 | c0001 | t0208 | g0014 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18977 | hp1 | a0001 | c0001 | t0201 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18977 | hp2 | a0002 | c0002 | t0098 | g0039 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18979 | hp1 | a0001 | c0001 | t0023 | g0218 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18979 | hp2 | a0002 | c0002 | t0101 | g0205 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18981 | hp1 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18982 | hp1 | a0001 | c0001 | t0024 | g0230 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18982 | hp2 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18987 | hp1 | a0001 | c0001 | t0089 | g0016 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18987 | hp2 | a0001 | c0001 | t0075 | g0182 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18988 | hp1 | a0001 | c0001 | t0159 | g0048 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18988 | hp2 | a0001 | c0001 | t0010 | g0178 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18989 | hp2 | a0001 | c0001 | t0087 | g0034 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18990 | hp2 | a0002 | c0002 | t0015 | g0010 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18993 | hp1 | a0002 | c0002 | t0015 | g0040 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18994 | hp1 | a0001 | c0001 | t0085 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18994 | hp2 | a0001 | c0001 | t0158 | g0222 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18995 | hp2 | a0001 | c0001 | t0207 | g0111 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18998 | hp2 | a0001 | c0001 | t0055 | g0005 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18999 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18999 | hp2 | a0001 | c0001 | t0176 | g0267 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19001 | hp1 | a0001 | c0001 | t0079 | g0183 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19003 | hp1 | a0001 | c0001 | t0170 | g0042 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19003 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19004 | hp1 | a0001 | c0001 | t0016 | g0081 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19004 | hp2 | a0001 | c0001 | t0047 | g0257 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19005 | hp2 | a0001 | c0001 | t0057 | g0109 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19007 | hp2 | a0001 | c0001 | t0080 | g0177 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19009 | hp1 | a0002 | c0002 | t0099 | g0039 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19009 | hp2 | a0001 | c0001 | t0078 | g0184 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19010 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19011 | hp2 | a0001 | c0001 | t0046 | g0020 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19012 | hp1 | a0001 | c0001 | t0209 | g0120 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19012 | hp2 | a0001 | c0001 | t0033 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | LWK | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | LWK | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19054 | hp1 | a0001 | c0001 | t0059 | g0014 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19054 | hp2 | a0001 | c0001 | t0141 | g0092 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19055 | hp1 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19056 | hp1 | a0002 | c0002 | t0093 | g0201 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19056 | hp2 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19058 | hp2 | a0002 | c0002 | t0091 | g0010 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19060 | hp1 | a0001 | c0001 | t0021 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19060 | hp2 | a0001 | c0001 | t0056 | g0016 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19062 | hp2 | a0001 | c0001 | t0203 | g0139 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19063 | hp2 | a0001 | c0001 | t0205 | g0119 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19068 | hp1 | a0001 | c0001 | t0025 | g0227 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19068 | hp2 | a0001 | c0001 | t0165 | g0246 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19070 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19070 | hp2 | a0001 | c0001 | t0138 | g0012 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19072 | hp1 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19072 | hp2 | a0002 | c0002 | t0094 | g0207 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19077 | hp1 | a0001 | c0001 | t0046 | g0273 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19077 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19078 | hp1 | a0001 | c0001 | t0160 | g0217 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19078 | hp2 | a0001 | c0001 | t0139 | g0022 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19079 | hp1 | a0001 | c0001 | t0210 | g0122 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19079 | hp2 | a0001 | c0001 | t0045 | g0006 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19080 | hp2 | a0001 | c0001 | t0021 | g0097 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19084 | hp1 | a0001 | c0001 | t0021 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19084 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19086 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19087 | hp1 | a0001 | c0001 | t0164 | g0254 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19087 | hp2 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19088 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19088 | hp2 | a0001 | c0001 | t0145 | g0095 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19089 | hp2 | a0001 | c0001 | t0012 | g0160 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19090 | hp1 | a0001 | c0001 | t0077 | g0019 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20129 | hp1 | a0001 | c0001 | t0130 | g0021 | AFR | ASW | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20129 | hp2 | a0001 | c0001 | t0122 | g0069 | AFR | ASW | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20752 | hp1 | a0001 | c0001 | t0044 | g0032 | EUR | TSI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20752 | hp2 | a0001 | c0001 | t0166 | g0235 | EUR | TSI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20805 | hp1 | a0001 | c0001 | t0013 | g0001 | EUR | TSI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0234 | EUR | TSI | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20905 | hp1 | a0002 | c0002 | t0035 | g0203 | SAS | GIH | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA20905 | hp2 | a0001 | c0001 | t0156 | g0163 | SAS | GIH | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG01123 | hp2 | a0001 | c0001 | t0026 | g0158 | AMR | CLM | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02109 | hp1 | a0001 | c0001 | t0172 | g0255 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02109 | hp2 | a0005 | c0005 | t0019 | g0041 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02486 | hp1 | a0001 | c0001 | t0071 | g0192 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02486 | hp2 | a0001 | c0001 | t0129 | g0021 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02559 | hp1 | a0001 | c0001 | t0119 | g0067 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG02559 | hp2 | a0004 | c0004 | t0111 | g0023 | AFR | ACB | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG03471 | hp2 | a0001 | c0001 | t0028 | g0074 | AFR | MSL | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | USA | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
HG06807 | hp2 | a0001 | c0001 | t0121 | g0053 | AFR | USA | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18955 | hp1 | a0001 | c0001 | t0058 | g0001 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
NA18955 | hp2 | a0001 | c0001 | t0175 | g0221 | EAS | JPT | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
homoSapiens | chm13v2 | a0001 | c0006 | t0047 | g0050 | REF | REF | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0009 | REF | REF | CEP43_chr6_166994397_167057718 | CEP43 | chr6 | 166994397 | 167057718 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:166999425 | G | A | 1 | a0003 | 8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.13G>A | p.Ala5Thr | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/13 | 29/13956 | 13/1200 | 5/399 | chr6 | 166999425 | |||
chr6:167003725 | C | T | 1 | a0006 | 1 | HG00597.hp2 | missense_variant&splice_region_variant | MODERATE | c.214C>T | p.Arg72Cys | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 4/13 | 230/13956 | 214/1200 | 72/399 | chr6 | 167003725 | |||
chr6:167013557 | C | G | 1 | a0004 | 6 | HG00642.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
missense_variant | MODERATE | c.569C>G | p.Ala190Gly | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/13 | 585/13956 | 569/1200 | 190/399 | chr6 | 167013557 | |||
chr6:167022440 | C | T | 2 | a0002 a0006 |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
missense_variant | MODERATE | c.611C>T | p.Thr204Ile | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/13 | 627/13956 | 611/1200 | 204/399 | chr6 | 167022440 | |||
chr6:167024788 | G | T | 2 | a0002 a0006 |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
missense_variant | MODERATE | c.813G>T | p.Lys271Asn | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/13 | 829/13956 | 813/1200 | 271/399 | chr6 | 167024788 | |||
chr6:167024804 | G | C | 1 | a0005 | 5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.829G>C | p.Ala277Pro | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/13 | 845/13956 | 829/1200 | 277/399 | chr6 | 167024804 | |||
chr6:167024876 | T | C | 2 | a0002 a0006 |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
missense_variant | MODERATE | c.901T>C | p.Ser301Pro | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/13 | 917/13956 | 901/1200 | 301/399 | chr6 | 167024876 |
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 |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:167040031 | A | AT | 156 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(153): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*65dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 66 | INFO_REALIGN_3_PRIME | chr6 | 167040031 | |||||
chr6:167040055 | C | G | 1 | a0002c0002t0103 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 77 | chr6 | 167040055 | ||||||
chr6:167040168 | T | G | 1 | a0001c0001t0037 | 2 | NA18941.hp1 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*190T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 190 | chr6 | 167040168 | ||||||
chr6:167040195 | A | G | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 217 | chr6 | 167040195 | ||||||
chr6:167040230 | C | T | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*252C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 252 | chr6 | 167040230 | ||||||
chr6:167040312 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*334G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 334 | chr6 | 167040312 | ||||||
chr6:167040313 | C | T | 1 | a0001c0001t0217 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 335 | chr6 | 167040313 | ||||||
chr6:167040344 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*366G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 366 | chr6 | 167040344 | ||||||
chr6:167040609 | A | C | 57 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(54): Show |
106 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*631A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 631 | chr6 | 167040609 | ||||||
chr6:167040728 | C | T | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*750C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 750 | chr6 | 167040728 | ||||||
chr6:167040749 | T | TATTCAGT others(4): Show |
90 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(87): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*772_*773insTTCAGT others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 773 | INFO_REALIGN_3_PRIME | chr6 | 167040749 | |||||
chr6:167040908 | T | C | 1 | a0001c0001t0104 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 930 | chr6 | 167040908 | ||||||
chr6:167040946 | G | A | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(47): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*968G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 968 | chr6 | 167040946 | ||||||
chr6:167040963 | T | C | 1 | a0001c0001t0180 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*985T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 985 | chr6 | 167040963 | ||||||
chr6:167041022 | AAAC | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1046_*1048delACA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1046 | INFO_REALIGN_3_PRIME | chr6 | 167041022 | |||||
chr6:167041029 | A | G | 1 | a0001c0001t0179 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1051 | chr6 | 167041029 | ||||||
chr6:167041065 | C | CT | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1087_*1088insT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1088 | chr6 | 167041065 | ||||||
chr6:167041108 | C | T | 3 | a0001c0001t0068 a0001c0001t0069 a0001c0001t0070 |
3 | HG02615.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1130C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1130 | chr6 | 167041108 | ||||||
chr6:167041109 | G | A | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG03688.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1131G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1131 | chr6 | 167041109 | ||||||
chr6:167041191 | C | T | 19 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0021 others(16): Show |
33 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1213C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1213 | chr6 | 167041191 | ||||||
chr6:167041374 | G | A | 11 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0031 others(8): Show |
19 | HG00597.hp1 HG00621.hp1 HG02027.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1396G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1396 | chr6 | 167041374 | ||||||
chr6:167041414 | C | T | 5 | a0001c0001t0028 a0001c0001t0064 a0001c0001t0065 others(2): Show |
6 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1436C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1436 | chr6 | 167041414 | ||||||
chr6:167041473 | C | T | 1 | a0001c0001t0216 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1495C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1495 | chr6 | 167041473 | ||||||
chr6:167041651 | A | G | 60 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(57): Show |
112 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1673A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1673 | chr6 | 167041651 | ||||||
chr6:167041682 | A | G | 3 | a0005c0005t0019 a0005c0005t0074 a0005c0005t0088 |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1704A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1704 | chr6 | 167041682 | ||||||
chr6:167041837 | C | T | 1 | a0001c0001t0132 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1859C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1859 | chr6 | 167041837 | ||||||
chr6:167041840 | G | T | 1 | a0001c0001t0215 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1862G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1862 | chr6 | 167041840 | ||||||
chr6:167041877 | A | G | 1 | a0001c0001t0087 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1899A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1899 | chr6 | 167041877 | ||||||
chr6:167041883 | A | G | 8 | a0001c0001t0127 a0001c0001t0128 a0001c0001t0129 others(5): Show |
8 | HG01243.hp1 HG02155.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1905A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1905 | chr6 | 167041883 | ||||||
chr6:167041886 | C | T | 16 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0032 others(13): Show |
26 | HG00408.hp1 HG00735.hp1 HG02004.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1908C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1908 | chr6 | 167041886 | ||||||
chr6:167041894 | G | A | 1 | a0001c0001t0071 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1916 | chr6 | 167041894 | ||||||
chr6:167041926 | C | T | 1 | a0001c0001t0084 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1948C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 1948 | chr6 | 167041926 | ||||||
chr6:167042057 | C | T | 1 | a0001c0001t0063 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2079C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2079 | chr6 | 167042057 | ||||||
chr6:167042141 | G | A | 112 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(109): Show |
165 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*2163G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2163 | chr6 | 167042141 | ||||||
chr6:167042207 | A | G | 1 | a0001c0001t0080 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2229A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2229 | chr6 | 167042207 | ||||||
chr6:167042356 | GTCTT | G | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2385_*2388delTTTC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2385 | INFO_REALIGN_3_PRIME | chr6 | 167042356 | |||||
chr6:167042380 | C | T | 2 | a0001c0001t0124 a0001c0001t0125 |
2 | HG02738.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2402C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2402 | chr6 | 167042380 | ||||||
chr6:167042388 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2410G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2410 | chr6 | 167042388 | ||||||
chr6:167042548 | C | T | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(45): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2570 | chr6 | 167042548 | ||||||
chr6:167042560 | A | G | 1 | a0001c0001t0121 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2582A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2582 | chr6 | 167042560 | ||||||
chr6:167042814 | T | TGTGTGTG others(24): Show |
1 | a0001c0001t0196 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836_*2837insGTGT others(27): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2837 | chr6 | 167042814 | ||||||
chr6:167042814 | T | TTG | 2 | a0001c0001t0029 a0001c0001t0084 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2860_*2861dupGT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTG | 6 | a0001c0001t0028 a0001c0001t0060 a0001c0001t0064 others(3): Show |
7 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2856_*2861dupGTGT others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0063 a0001c0001t0121 a0003c0003t0009 others(3): Show |
10 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2854_*2861dupGTGT others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(3): Show |
6 | a0001c0001t0008 a0001c0001t0047 a0001c0001t0077 others(3): Show |
10 | NA18982.hp2 NA18998.hp1 NA19001.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2852_*2861dupGTGT others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0126 a0006c0007t0090 |
2 | HG00597.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2850_*2861dupGTGT others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(7): Show |
16 | a0001c0001t0010 a0001c0001t0031 a0001c0001t0033 others(13): Show |
24 | HG00408.hp1 HG00597.hp1 HG01346.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2848_*2861dupGTGT others(10): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(9): Show |
32 | a0001c0001t0006 a0001c0001t0030 a0001c0001t0032 others(29): Show |
45 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2846_*2861dupGTGT others(12): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(11): Show |
19 | a0001c0001t0014 a0001c0001t0020 a0001c0001t0024 others(16): Show |
29 | HG00639.hp2 HG01255.hp2 HG02027.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2844_*2861dupGTGT others(14): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(13): Show |
45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(42): Show |
88 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2842_*2861dupGTGT others(16): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(15): Show |
30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(27): Show |
79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2840_*2861dupGTGT others(18): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(17): Show |
26 | a0001c0001t0012 a0001c0001t0022 a0001c0001t0037 others(23): Show |
36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2838_*2861dupGTGT others(20): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(19): Show |
10 | a0001c0001t0016 a0001c0001t0048 a0001c0001t0049 others(7): Show |
15 | HG00741.hp1 HG01074.hp2 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2861_*2862insGTGT others(22): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(21): Show |
5 | a0001c0001t0107 a0001c0001t0176 a0001c0001t0185 others(2): Show |
5 | HG01928.hp1 HG03130.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2861_*2862insGTGT others(24): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(23): Show |
1 | a0001c0001t0184 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2861_*2862insGTGT others(26): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(25): Show |
2 | a0001c0001t0148 a0001c0001t0183 |
2 | HG01993.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2861_*2862insGTGT others(28): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042814 | T | TTGTGTGT others(29): Show |
3 | a0001c0001t0054 a0001c0001t0182 a0001c0001t0197 |
4 | HG00738.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2861_*2862insGTGT others(32): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | INFO_REALIGN_3_PRIME | chr6 | 167042814 | |||||
chr6:167042840 | T | G | 1 | a0006c0007t0090 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2862T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2862 | chr6 | 167042840 | ||||||
chr6:167042921 | T | C | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2943T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2943 | chr6 | 167042921 | ||||||
chr6:167042925 | A | C | 1 | a0001c0001t0213 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2947A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 2947 | chr6 | 167042925 | ||||||
chr6:167042997 | G | A | 4 | a0001c0001t0048 a0001c0001t0185 a0001c0001t0187 others(1): Show |
5 | HG01069.hp1 HG01074.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3019G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3019 | chr6 | 167042997 | ||||||
chr6:167042998 | A | G | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3020A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3020 | chr6 | 167042998 | ||||||
chr6:167043002 | A | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3024A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3024 | chr6 | 167043002 | ||||||
chr6:167043298 | G | A | 18 | a0001c0001t0131 a0002c0002t0015 a0002c0002t0035 others(15): Show |
23 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3320G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3320 | chr6 | 167043298 | ||||||
chr6:167043352 | C | T | 1 | a0001c0001t0060 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3374C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3374 | chr6 | 167043352 | ||||||
chr6:167043353 | G | A | 3 | a0001c0001t0198 a0001c0001t0199 a0001c0001t0206 |
3 | HG01928.hp1 HG01934.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3375G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3375 | chr6 | 167043353 | ||||||
chr6:167043372 | C | T | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*3394C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3394 | chr6 | 167043372 | ||||||
chr6:167043375 | C | CT | 55 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(52): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3419dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3420 | INFO_REALIGN_3_PRIME | chr6 | 167043375 | |||||
chr6:167043375 | C | CTT | 6 | a0001c0001t0169 a0001c0001t0170 a0001c0001t0171 others(3): Show |
8 | HG00621.hp2 HG02109.hp2 HG02293.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3418_*3419dupTT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3420 | INFO_REALIGN_3_PRIME | chr6 | 167043375 | |||||
chr6:167043375 | CT | C | 126 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(123): Show |
211 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*3419delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3419 | INFO_REALIGN_3_PRIME | chr6 | 167043375 | |||||
chr6:167043446 | C | T | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3468C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3468 | chr6 | 167043446 | ||||||
chr6:167043571 | C | T | 1 | a0001c0001t0193 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3593 | chr6 | 167043571 | ||||||
chr6:167043617 | A | G | 1 | a0001c0001t0120 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3639A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3639 | chr6 | 167043617 | ||||||
chr6:167043642 | C | G | 2 | a0001c0001t0168 a0001c0001t0175 |
2 | NA18955.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3664C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3664 | chr6 | 167043642 | ||||||
chr6:167043674 | T | C | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3696T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3696 | chr6 | 167043674 | ||||||
chr6:167043747 | T | G | 1 | a0001c0001t0207 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3769T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3769 | chr6 | 167043747 | ||||||
chr6:167043831 | A | T | 1 | a0001c0001t0188 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3853A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3853 | chr6 | 167043831 | ||||||
chr6:167043888 | C | T | 16 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(13): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3910C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3910 | chr6 | 167043888 | ||||||
chr6:167043912 | T | G | 1 | a0001c0001t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3934T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3934 | chr6 | 167043912 | ||||||
chr6:167043933 | C | T | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3955C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3955 | chr6 | 167043933 | ||||||
chr6:167043934 | G | A | 3 | a0001c0001t0068 a0001c0001t0069 a0001c0001t0070 |
3 | HG02615.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3956G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 3956 | chr6 | 167043934 | ||||||
chr6:167043995 | G | GC | 2 | a0001c0001t0029 a0001c0001t0084 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4018dupC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4019 | INFO_REALIGN_3_PRIME | chr6 | 167043995 | |||||
chr6:167043997 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4019G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4019 | chr6 | 167043997 | ||||||
chr6:167044047 | GAC | G | 2 | a0001c0001t0055 a0001c0001t0201 |
3 | NA18946.hp2 NA18977.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4073_*4074delCA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4073 | INFO_REALIGN_3_PRIME | chr6 | 167044047 | |||||
chr6:167044106 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4128G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4128 | chr6 | 167044106 | ||||||
chr6:167044109 | A | G | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4131A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4131 | chr6 | 167044109 | ||||||
chr6:167044126 | A | C | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4148A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4148 | chr6 | 167044126 | ||||||
chr6:167044135 | G | A | 1 | a0002c0002t0095 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4157G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4157 | chr6 | 167044135 | ||||||
chr6:167044146 | C | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4168C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4168 | chr6 | 167044146 | ||||||
chr6:167044151 | A | G | 1 | a0001c0001t0174 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4173A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4173 | chr6 | 167044151 | ||||||
chr6:167044196 | C | A | 2 | a0001c0001t0105 a0001c0001t0106 |
2 | HG03688.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4218C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4218 | chr6 | 167044196 | ||||||
chr6:167044232 | G | A | 1 | a0001c0001t0021 | 3 | NA19060.hp1 NA19080.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4254G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4254 | chr6 | 167044232 | ||||||
chr6:167044267 | A | G | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4289A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4289 | chr6 | 167044267 | ||||||
chr6:167044334 | C | T | 1 | a0001c0001t0159 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4356C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4356 | chr6 | 167044334 | ||||||
chr6:167044434 | G | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4456G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4456 | chr6 | 167044434 | ||||||
chr6:167044522 | G | C | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4544G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4544 | chr6 | 167044522 | ||||||
chr6:167044590 | C | A | 17 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(14): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4612C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4612 | chr6 | 167044590 | ||||||
chr6:167044590 | C | T | 4 | a0001c0001t0029 a0001c0001t0071 a0001c0001t0072 others(1): Show |
5 | HG02258.hp2 HG02486.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4612C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4612 | chr6 | 167044590 | ||||||
chr6:167044664 | C | T | 2 | a0001c0001t0071 a0001c0001t0072 |
2 | HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4686C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4686 | chr6 | 167044664 | ||||||
chr6:167044787 | C | T | 1 | a0001c0001t0171 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4809C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4809 | chr6 | 167044787 | ||||||
chr6:167044853 | G | A | 16 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(13): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4875G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4875 | chr6 | 167044853 | ||||||
chr6:167044875 | C | T | 1 | a0001c0001t0027 | 2 | HG00099.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4897C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4897 | chr6 | 167044875 | ||||||
chr6:167044967 | G | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4989G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 4989 | chr6 | 167044967 | ||||||
chr6:167045001 | C | T | 1 | a0004c0004t0111 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5023C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5023 | chr6 | 167045001 | ||||||
chr6:167045090 | A | AGCC | 62 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(59): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*5112_*5113insGCC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5113 | chr6 | 167045090 | ||||||
chr6:167045098 | A | AT | 60 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(57): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*5130dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5131 | INFO_REALIGN_3_PRIME | chr6 | 167045098 | |||||
chr6:167045109 | C | T | 2 | a0001c0001t0178 a0002c0002t0092 |
2 | HG02145.hp2 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5131C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5131 | chr6 | 167045109 | ||||||
chr6:167045110 | C | T | 60 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(57): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*5132C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5132 | chr6 | 167045110 | ||||||
chr6:167045140 | G | A | 3 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5162G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5162 | chr6 | 167045140 | ||||||
chr6:167045148 | T | G | 1 | a0001c0001t0051 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5170T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5170 | chr6 | 167045148 | ||||||
chr6:167045211 | C | G | 3 | a0001c0001t0041 a0001c0001t0116 a0001c0001t0119 |
4 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5233C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5233 | chr6 | 167045211 | ||||||
chr6:167045304 | G | A | 61 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(58): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*5326G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5326 | chr6 | 167045304 | ||||||
chr6:167045324 | G | T | 1 | a0001c0001t0063 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5346G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5346 | chr6 | 167045324 | ||||||
chr6:167045346 | C | T | 2 | a0001c0001t0054 a0001c0001t0197 |
3 | HG01175.hp1 HG01257.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5368C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5368 | chr6 | 167045346 | ||||||
chr6:167045359 | G | GC | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(49): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*5389dupC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5390 | INFO_REALIGN_3_PRIME | chr6 | 167045359 | |||||
chr6:167045359 | G | GCC | 18 | a0001c0001t0005 a0001c0001t0045 a0001c0001t0046 others(15): Show |
26 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5388_*5389dupCC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5390 | INFO_REALIGN_3_PRIME | chr6 | 167045359 | |||||
chr6:167045361 | C | T | 1 | a0001c0001t0072 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5383C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5383 | chr6 | 167045361 | ||||||
chr6:167045365 | C | G | 19 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(16): Show |
33 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5387C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5387 | chr6 | 167045365 | ||||||
chr6:167045454 | G | A | 3 | a0001c0001t0055 a0001c0001t0078 a0001c0001t0201 |
4 | NA18946.hp2 NA18977.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5476G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5476 | chr6 | 167045454 | ||||||
chr6:167045651 | C | T | 13 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(10): Show |
18 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5673C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5673 | chr6 | 167045651 | ||||||
chr6:167045692 | G | A | 4 | a0003c0003t0009 a0003c0003t0081 a0003c0003t0082 others(1): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5714G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5714 | chr6 | 167045692 | ||||||
chr6:167045721 | C | T | 1 | a0002c0002t0103 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5743C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5743 | chr6 | 167045721 | ||||||
chr6:167045737 | A | AAAC | 3 | a0001c0001t0150 a0001c0001t0153 a0001c0001t0154 |
3 | HG00323.hp2 HG00741.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5772_*5774dupAAC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5775 | INFO_REALIGN_3_PRIME | chr6 | 167045737 | |||||
chr6:167045753 | G | GA | 5 | a0001c0001t0138 a0001c0001t0163 a0001c0001t0191 others(2): Show |
5 | NA18947.hp2 NA18949.hp2 NA18977.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5781dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5782 | INFO_REALIGN_3_PRIME | chr6 | 167045753 | |||||
chr6:167045761 | G | A | 1 | a0001c0001t0076 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5783G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 5783 | chr6 | 167045761 | ||||||
chr6:167046026 | C | T | 1 | a0002c0002t0097 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6048C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6048 | chr6 | 167046026 | ||||||
chr6:167046108 | C | T | 60 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(57): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*6130C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6130 | chr6 | 167046108 | ||||||
chr6:167046205 | AT | A | 72 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(69): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*6228delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6228 | chr6 | 167046205 | ||||||
chr6:167046495 | A | G | 2 | a0001c0001t0027 a0001c0001t0062 |
3 | HG00099.hp2 HG00280.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6517A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6517 | chr6 | 167046495 | ||||||
chr6:167046604 | C | A | 1 | a0001c0001t0028 | 2 | HG03195.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6626C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6626 | chr6 | 167046604 | ||||||
chr6:167046673 | G | A | 1 | a0002c0002t0100 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6695G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6695 | chr6 | 167046673 | ||||||
chr6:167046747 | G | A | 2 | a0001c0001t0029 a0001c0001t0084 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6769G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 6769 | chr6 | 167046747 | ||||||
chr6:167047036 | G | T | 1 | a0001c0001t0061 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7058G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7058 | chr6 | 167047036 | ||||||
chr6:167047049 | A | G | 72 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(69): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*7071A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7071 | chr6 | 167047049 | ||||||
chr6:167047086 | T | C | 2 | a0001c0001t0192 a0001c0001t0210 |
2 | NA18946.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7108T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7108 | chr6 | 167047086 | ||||||
chr6:167047230 | G | A | 72 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(69): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*7252G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7252 | chr6 | 167047230 | ||||||
chr6:167047232 | A | G | 1 | a0001c0001t0066 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7254A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7254 | chr6 | 167047232 | ||||||
chr6:167047241 | C | T | 1 | a0001c0001t0063 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7263C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7263 | chr6 | 167047241 | ||||||
chr6:167047329 | A | G | 1 | a0001c0001t0213 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7351A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7351 | chr6 | 167047329 | ||||||
chr6:167047392 | T | A | 1 | a0001c0001t0086 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7414T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7414 | chr6 | 167047392 | ||||||
chr6:167047400 | AAGTTATT others(7): Show |
A | 72 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(69): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*7426_*7439delTATT others(10): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7426 | INFO_REALIGN_3_PRIME | chr6 | 167047400 | |||||
chr6:167047542 | A | G | 1 | a0002c0002t0092 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7564A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7564 | chr6 | 167047542 | ||||||
chr6:167047702 | G | C | 1 | a0001c0001t0164 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7724G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7724 | chr6 | 167047702 | ||||||
chr6:167047897 | C | G | 3 | a0005c0005t0019 a0005c0005t0074 a0005c0005t0088 |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7919C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7919 | chr6 | 167047897 | ||||||
chr6:167047913 | C | A | 1 | a0001c0001t0128 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7935C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7935 | chr6 | 167047913 | ||||||
chr6:167047935 | T | C | 1 | a0001c0001t0204 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7957T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 7957 | chr6 | 167047935 | ||||||
chr6:167048013 | G | A | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*8035G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8035 | chr6 | 167048013 | ||||||
chr6:167048074 | C | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*8096C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8096 | chr6 | 167048074 | ||||||
chr6:167048157 | A | G | 72 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(69): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*8179A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8179 | chr6 | 167048157 | ||||||
chr6:167048175 | G | C | 15 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(12): Show |
20 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8197G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8197 | chr6 | 167048175 | ||||||
chr6:167048187 | TTG | T | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*8212_*8213delTG | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8212 | INFO_REALIGN_3_PRIME | chr6 | 167048187 | |||||
chr6:167048258 | A | G | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*8280A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8280 | chr6 | 167048258 | ||||||
chr6:167048336 | CT | C | 15 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(12): Show |
20 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8359delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8359 | chr6 | 167048336 | ||||||
chr6:167048477 | T | G | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*8499T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8499 | chr6 | 167048477 | ||||||
chr6:167048487 | A | G | 1 | a0001c0001t0126 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8509A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8509 | chr6 | 167048487 | ||||||
chr6:167048841 | A | T | 1 | a0005c0005t0074 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8863A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 8863 | chr6 | 167048841 | ||||||
chr6:167049155 | G | A | 3 | a0001c0001t0043 a0001c0001t0133 a0001c0001t0188 |
4 | HG01192.hp2 HG01257.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9177G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 9177 | chr6 | 167049155 | ||||||
chr6:167049373 | C | T | 1 | a0002c0002t0093 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9395C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 9395 | chr6 | 167049373 | ||||||
chr6:167049666 | A | T | 2 | a0001c0001t0044 a0001c0001t0139 |
3 | HG00099.hp1 NA19078.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9688A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 9688 | chr6 | 167049666 | ||||||
chr6:167049943 | T | C | 4 | a0001c0001t0023 a0001c0001t0046 a0001c0001t0161 others(1): Show |
7 | HG02129.hp1 NA18942.hp2 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9965T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 9965 | chr6 | 167049943 | ||||||
chr6:167050188 | T | TA | 3 | a0005c0005t0019 a0005c0005t0074 a0005c0005t0088 |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10212dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10213 | INFO_REALIGN_3_PRIME | chr6 | 167050188 | |||||
chr6:167050207 | C | T | 5 | a0001c0001t0040 a0001c0001t0108 a0001c0001t0110 others(2): Show |
6 | HG01099.hp2 HG01243.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10229C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10229 | chr6 | 167050207 | ||||||
chr6:167050414 | T | C | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*10436T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10436 | chr6 | 167050414 | ||||||
chr6:167050426 | G | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*10448G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10448 | chr6 | 167050426 | ||||||
chr6:167050502 | C | T | 15 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(12): Show |
20 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10524C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10524 | chr6 | 167050502 | ||||||
chr6:167050745 | C | T | 4 | a0003c0003t0009 a0003c0003t0081 a0003c0003t0082 others(1): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10767C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10767 | chr6 | 167050745 | ||||||
chr6:167050775 | A | G | 6 | a0001c0001t0028 a0001c0001t0063 a0001c0001t0064 others(3): Show |
7 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10797A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10797 | chr6 | 167050775 | ||||||
chr6:167050776 | AAAAAG | A | 5 | a0001c0001t0028 a0001c0001t0063 a0001c0001t0065 others(2): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10803_*10807delGA others(3): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10803 | INFO_REALIGN_3_PRIME | chr6 | 167050776 | |||||
chr6:167050781 | G | GA | 8 | a0001c0001t0129 a0001c0001t0131 a0001c0001t0139 others(5): Show |
8 | HG00741.hp2 HG01175.hp1 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10826dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10827 | INFO_REALIGN_3_PRIME | chr6 | 167050781 | |||||
chr6:167050781 | GA | G | 17 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(14): Show |
26 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*10826delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10826 | INFO_REALIGN_3_PRIME | chr6 | 167050781 | |||||
chr6:167050781 | GAAAAA | G | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(39): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*10822_*10826delAA others(3): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10822 | INFO_REALIGN_3_PRIME | chr6 | 167050781 | |||||
chr6:167050781 | GAAAAAA | G | 5 | a0001c0001t0075 a0001c0001t0085 a0001c0001t0154 others(2): Show |
7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10821_*10826delAA others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10821 | INFO_REALIGN_3_PRIME | chr6 | 167050781 | |||||
chr6:167050781 | GAAAAAAA | G | 14 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(11): Show |
27 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*10820_*10826delAA others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10820 | INFO_REALIGN_3_PRIME | chr6 | 167050781 | |||||
chr6:167050804 | A | G | 2 | a0005c0005t0019 a0005c0005t0088 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10826A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10826 | chr6 | 167050804 | ||||||
chr6:167050958 | T | C | 1 | a0001c0001t0166 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10980T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 10980 | chr6 | 167050958 | ||||||
chr6:167051014 | G | C | 3 | a0001c0001t0150 a0001c0001t0153 a0001c0001t0154 |
3 | HG00323.hp2 HG00741.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11036G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11036 | chr6 | 167051014 | ||||||
chr6:167051142 | G | A | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*11164G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11164 | chr6 | 167051142 | ||||||
chr6:167051192 | T | G | 3 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11214T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11214 | chr6 | 167051192 | ||||||
chr6:167051386 | A | G | 2 | a0001c0001t0029 a0001c0001t0084 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11408A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11408 | chr6 | 167051386 | ||||||
chr6:167051468 | G | A | 1 | a0001c0001t0128 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11490G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11490 | chr6 | 167051468 | ||||||
chr6:167051611 | C | G | 4 | a0001c0001t0057 a0001c0001t0059 a0001c0001t0208 others(1): Show |
6 | HG02074.hp1 NA18940.hp2 NA18975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11633C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11633 | chr6 | 167051611 | ||||||
chr6:167051645 | T | C | 1 | a0001c0001t0162 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11667T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11667 | chr6 | 167051645 | ||||||
chr6:167051842 | A | T | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*11864A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11864 | chr6 | 167051842 | ||||||
chr6:167051900 | ATTGT | A | 2 | a0001c0001t0029 a0001c0001t0084 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11925_*11928delGT others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 11925 | INFO_REALIGN_3_PRIME | chr6 | 167051900 | |||||
chr6:167052005 | T | G | 16 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0030 others(13): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*12027T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12027 | chr6 | 167052005 | ||||||
chr6:167052029 | TTAAG | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*12054_*12057delAG others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12054 | INFO_REALIGN_3_PRIME | chr6 | 167052029 | |||||
chr6:167052088 | G | A | 73 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(70): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*12110G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12110 | chr6 | 167052088 | ||||||
chr6:167052286 | C | A | 89 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(86): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*12308C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12308 | chr6 | 167052286 | ||||||
chr6:167052394 | C | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*12416C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12416 | chr6 | 167052394 | ||||||
chr6:167052435 | G | T | 1 | a0001c0001t0112 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12457G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12457 | chr6 | 167052435 | ||||||
chr6:167052478 | C | T | 1 | a0001c0001t0121 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12500C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12500 | chr6 | 167052478 | ||||||
chr6:167052570 | G | C | 15 | a0002c0002t0015 a0002c0002t0035 a0002c0002t0036 others(12): Show |
20 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*12592G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12592 | chr6 | 167052570 | ||||||
chr6:167052602 | T | G | 10 | a0001c0001t0071 a0001c0001t0072 a0001c0001t0073 others(7): Show |
16 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*12624T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12624 | chr6 | 167052602 | ||||||
chr6:167052662 | G | T | 46 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(43): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*12684G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 13/13 | 12684 | chr6 | 167052662 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:166999644 | GC | G | 95 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(92): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.102+134delC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 166999644 | ||||||
chr6:166999742 | A | G | 154 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(151): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.102+228A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/12 | chr6 | 166999742 | |||||||
chr6:166999963 | C | T | 4 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0074g0208 others(1): Show |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-97C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/12 | chr6 | 166999963 | |||||||
chr6:166999994 | A | C | 4 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0074g0208 others(1): Show |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-66A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/12 | chr6 | 166999994 | |||||||
chr6:167000051 | T | C | 92 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(89): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.103-9T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 1/12 | chr6 | 167000051 | |||||||
chr6:167000170 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.156+57C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000170 | |||||||
chr6:167000214 | G | C | 1 | a0001c0001t0017g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.156+101G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000214 | |||||||
chr6:167000241 | C | T | 34 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(31): Show |
38 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+128C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000241 | |||||||
chr6:167000252 | A | T | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+139A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000252 | |||||||
chr6:167000348 | A | G | 1 | a0001c0001t0044g0032 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.156+235A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000348 | |||||||
chr6:167000557 | A | G | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+444A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000557 | |||||||
chr6:167000565 | G | A | 34 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(31): Show |
38 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+452G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000565 | |||||||
chr6:167000653 | C | T | 34 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(31): Show |
38 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+540C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000653 | |||||||
chr6:167000690 | C | T | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+577C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000690 | |||||||
chr6:167000768 | G | A | 22 | a0001c0001t0020g0054 a0001c0001t0020g0056 a0001c0001t0020g0063 others(19): Show |
22 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.156+655G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000768 | |||||||
chr6:167000802 | C | T | 27 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(24): Show |
30 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.156+689C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000802 | |||||||
chr6:167000837 | C | G | 1 | a0001c0001t0046g0273 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.156+724C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000837 | |||||||
chr6:167000873 | T | G | 1 | a0001c0001t0005g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.156+760T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000873 | |||||||
chr6:167000896 | A | ACT | 34 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(31): Show |
38 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+786_156+787dup others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 167000896 | ||||||
chr6:167000945 | C | A | 13 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(10): Show |
16 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+832C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167000945 | |||||||
chr6:167001042 | T | G | 3 | a0001c0001t0118g0072 a0001c0001t0120g0073 a0001c0001t0131g0071 |
3 | HG02572.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.156+929T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001042 | |||||||
chr6:167001043 | T | C | 3 | a0001c0001t0118g0072 a0001c0001t0120g0073 a0001c0001t0131g0071 |
3 | HG02572.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.156+930T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001043 | |||||||
chr6:167001193 | G | A | 326 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(323): Show |
356 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.156+1080G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001193 | |||||||
chr6:167001281 | G | T | 1 | a0001c0001t0173g0272 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.156+1168G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001281 | |||||||
chr6:167001494 | A | G | 1 | a0004c0004t0114g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.156+1381A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001494 | |||||||
chr6:167001526 | A | G | 1 | a0001c0001t0007g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.156+1413A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001526 | |||||||
chr6:167001603 | A | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+1490A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001603 | |||||||
chr6:167001736 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-1457T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001736 | |||||||
chr6:167001787 | C | T | 38 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(35): Show |
45 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.157-1406C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001787 | |||||||
chr6:167001915 | C | CT | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.157-1277dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 167001915 | ||||||
chr6:167001952 | C | A | 153 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(150): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.157-1241C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001952 | |||||||
chr6:167001966 | C | T | 1 | a0001c0001t0169g0271 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.157-1227C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001966 | |||||||
chr6:167001968 | C | G | 1 | a0001c0001t0128g0162 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157-1225C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167001968 | |||||||
chr6:167002117 | A | G | 14 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(11): Show |
17 | HG01099.hp2 HG01109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.157-1076A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002117 | |||||||
chr6:167002142 | G | A | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-1051G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002142 | |||||||
chr6:167002267 | G | A | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-926G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002267 | |||||||
chr6:167002343 | A | G | 1 | a0001c0001t0010g0188 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.157-850A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002343 | |||||||
chr6:167002721 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-472T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002721 | |||||||
chr6:167002874 | C | T | 2 | a0001c0001t0122g0069 a0001c0001t0123g0070 |
2 | HG03704.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.157-319C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167002874 | |||||||
chr6:167003003 | C | A | 4 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-190C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 2/12 | chr6 | 167003003 | |||||||
chr6:167003287 | T | C | 2 | a0002c0002t0098g0039 a0002c0002t0099g0039 |
2 | NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.211+40T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | chr6 | 167003287 | |||||||
chr6:167003358 | G | C | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.211+111G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | chr6 | 167003358 | |||||||
chr6:167003376 | A | G | 4 | a0001c0001t0151g0270 a0001c0001t0176g0267 a0001c0001t0177g0268 others(1): Show |
4 | NA18940.hp1 NA18949.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+129A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | chr6 | 167003376 | |||||||
chr6:167003623 | AC | A | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-98delC | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 167003623 | ||||||
chr6:167003685 | G | A | 46 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(43): Show |
51 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.212-38G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | chr6 | 167003685 | |||||||
chr6:167003703 | C | CT | 5 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0266 others(2): Show |
5 | HG02040.hp1 HG02129.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-15dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 167003703 | ||||||
chr6:167004063 | G | T | 149 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(146): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.301-201G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 4/12 | chr6 | 167004063 | |||||||
chr6:167004237 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.301-27G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 4/12 | chr6 | 167004237 | |||||||
chr6:167004438 | T | G | 1 | a0001c0001t0041g0051 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.438+37T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004438 | |||||||
chr6:167004447 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+46G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004447 | |||||||
chr6:167004496 | C | G | 1 | a0001c0001t0012g0160 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.438+95C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004496 | |||||||
chr6:167004507 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.438+106A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004507 | |||||||
chr6:167004613 | TTTGATCC others(62): Show |
T | 167 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(164): Show |
184 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.438+222_438+290del others(69): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167004613 | ||||||
chr6:167004691 | CCATT | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+296_438+299del others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167004691 | ||||||
chr6:167004867 | G | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+466G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004867 | |||||||
chr6:167004945 | C | T | 46 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(43): Show |
51 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.438+544C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167004945 | |||||||
chr6:167005033 | C | T | 1 | a0001c0001t0017g0261 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.438+632C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005033 | |||||||
chr6:167005336 | C | T | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.438+935C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005336 | |||||||
chr6:167005443 | T | C | 10 | a0001c0001t0004g0012 a0001c0001t0004g0079 a0001c0001t0004g0080 others(7): Show |
10 | HG00544.hp2 HG02083.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.438+1042T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005443 | |||||||
chr6:167005616 | A | C | 29 | a0001c0001t0020g0054 a0001c0001t0020g0056 a0001c0001t0020g0063 others(26): Show |
29 | HG01123.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.438+1215A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005616 | |||||||
chr6:167005617 | G | A | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.438+1216G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005617 | |||||||
chr6:167005692 | C | T | 4 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+1291C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005692 | |||||||
chr6:167005706 | A | G | 4 | a0001c0001t0041g0051 a0001c0001t0061g0066 a0001c0001t0116g0068 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+1305A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005706 | |||||||
chr6:167005731 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+1330A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005731 | |||||||
chr6:167005803 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+1402T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005803 | |||||||
chr6:167005907 | G | A | 1 | a0001c0001t0204g0085 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.438+1506G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005907 | |||||||
chr6:167005922 | A | C | 1 | a0001c0001t0187g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.438+1521A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005922 | |||||||
chr6:167005983 | G | C | 43 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(40): Show |
47 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.438+1582G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167005983 | |||||||
chr6:167006001 | C | G | 1 | a0001c0001t0107g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.438+1600C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006001 | |||||||
chr6:167006019 | A | T | 1 | a0001c0001t0041g0175 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.438+1618A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006019 | |||||||
chr6:167006050 | G | A | 1 | a0006c0007t0090g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.438+1649G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006050 | |||||||
chr6:167006060 | G | T | 1 | a0001c0001t0004g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.438+1659G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006060 | |||||||
chr6:167006061 | T | C | 1 | a0001c0001t0156g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.438+1660T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006061 | |||||||
chr6:167006171 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+1770T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006171 | |||||||
chr6:167006183 | T | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+1782T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006183 | |||||||
chr6:167006285 | G | A | 3 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.438+1884G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006285 | |||||||
chr6:167006576 | CTATT | C | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.438+2179_438+2182d others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167006576 | ||||||
chr6:167006701 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+2300A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006701 | |||||||
chr6:167006704 | G | A | 1 | a0002c0002t0103g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.438+2303G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167006704 | |||||||
chr6:167007082 | A | G | 5 | a0001c0001t0040g0024 a0001c0001t0040g0025 a0001c0001t0110g0161 others(2): Show |
5 | HG01099.hp2 HG01243.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+2681A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007082 | |||||||
chr6:167007139 | G | T | 3 | a0003c0003t0009g0038 a0003c0003t0009g0189 a0003c0003t0083g0190 |
4 | HG02622.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+2738G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007139 | |||||||
chr6:167007306 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.438+2905G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007306 | |||||||
chr6:167007339 | A | T | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+2938A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007339 | |||||||
chr6:167007403 | A | G | 1 | a0001c0001t0030g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.438+3002A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007403 | |||||||
chr6:167007591 | A | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+3190A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007591 | |||||||
chr6:167007594 | G | GTT | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+3196_438+3197d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167007594 | ||||||
chr6:167007599 | C | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.438+3198C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167007599 | |||||||
chr6:167008086 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.439-2727T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008086 | |||||||
chr6:167008123 | GT | G | 118 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(115): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.439-2676delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167008123 | ||||||
chr6:167008123 | GTT | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-2677_439-2676d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167008123 | ||||||
chr6:167008331 | A | G | 1 | a0001c0001t0049g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.439-2482A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008331 | |||||||
chr6:167008359 | CCTT | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.439-2451_439-2449d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167008359 | ||||||
chr6:167008421 | G | A | 1 | a0001c0001t0149g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.439-2392G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008421 | |||||||
chr6:167008463 | A | AT | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-2341dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167008463 | ||||||
chr6:167008629 | G | A | 2 | a0001c0001t0118g0072 a0001c0001t0131g0071 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.439-2184G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008629 | |||||||
chr6:167008665 | C | T | 1 | a0002c0002t0103g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.439-2148C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008665 | |||||||
chr6:167008720 | C | T | 1 | a0001c0001t0006g0260 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.439-2093C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008720 | |||||||
chr6:167008727 | G | A | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.439-2086G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008727 | |||||||
chr6:167008796 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.439-2017T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008796 | |||||||
chr6:167008799 | T | G | 1 | a0001c0001t0173g0272 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.439-2014T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167008799 | |||||||
chr6:167009024 | G | A | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-1789G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009024 | |||||||
chr6:167009073 | A | G | 1 | a0001c0001t0180g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.439-1740A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009073 | |||||||
chr6:167009115 | GGCGCGGT others(13): Show |
G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(164): Show |
184 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.439-1697_439-1678d others(22): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009115 | |||||||
chr6:167009189 | C | T | 28 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(25): Show |
31 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.439-1624C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009189 | |||||||
chr6:167009298 | C | T | 3 | a0001c0001t0006g0258 a0001c0001t0006g0259 a0001c0001t0047g0257 |
3 | HG00438.hp2 NA19004.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.439-1515C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009298 | |||||||
chr6:167009324 | A | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(94): Show |
110 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.439-1489A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009324 | |||||||
chr6:167009346 | C | G | 1 | a0001c0001t0215g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.439-1467C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009346 | |||||||
chr6:167009434 | C | T | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.439-1379C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009434 | |||||||
chr6:167009499 | CAA | C | 42 | a0001c0001t0001g0103 a0001c0001t0002g0043 a0001c0001t0002g0214 others(39): Show |
47 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.439-1285_439-1284d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009499 | ||||||
chr6:167009499 | CAAA | C | 175 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0106 others(172): Show |
185 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.439-1286_439-1284d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009499 | ||||||
chr6:167009499 | CAAAA | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
87 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.439-1287_439-1284d others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009499 | ||||||
chr6:167009499 | CAAAAA | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0011g0031 others(2): Show |
6 | HG00323.hp1 HG01256.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.439-1288_439-1284d others(7): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009499 | ||||||
chr6:167009527 | AAAT | A | 10 | a0002c0002t0015g0010 a0002c0002t0035g0203 a0002c0002t0091g0010 others(7): Show |
10 | HG02080.hp2 HG02145.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.439-1284_439-1282d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009527 | ||||||
chr6:167009528 | AAT | A | 11 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(8): Show |
11 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-1283_439-1282d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009528 | ||||||
chr6:167009559 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-1254G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009559 | |||||||
chr6:167009580 | G | A | 1 | a0005c0005t0074g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.439-1233G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009580 | |||||||
chr6:167009623 | C | T | 1 | a0001c0001t0043g0030 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.439-1190C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009623 | |||||||
chr6:167009642 | A | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-1171A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009642 | |||||||
chr6:167009665 | C | CA | 55 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0010g0002 others(52): Show |
61 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.439-1128dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009665 | ||||||
chr6:167009665 | CA | C | 23 | a0001c0001t0001g0017 a0001c0001t0001g0147 a0001c0001t0001g0151 others(20): Show |
25 | HG00323.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.439-1128delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009665 | ||||||
chr6:167009712 | T | C | 1 | a0001c0001t0065g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.439-1101T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009712 | |||||||
chr6:167009785 | G | A | 1 | a0002c0002t0100g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.439-1028G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009785 | |||||||
chr6:167009833 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-980T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009833 | |||||||
chr6:167009844 | GAAAAATA | G | 4 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0074g0208 others(1): Show |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-965_439-959del others(7): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009844 | ||||||
chr6:167009846 | A | AAGAT | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-966_439-965ins others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167009846 | ||||||
chr6:167009856 | A | G | 1 | a0001c0001t0006g0252 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.439-957A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167009856 | |||||||
chr6:167010054 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-759A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010054 | |||||||
chr6:167010071 | G | A | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.439-742G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010071 | |||||||
chr6:167010093 | T | C | 1 | a0001c0001t0014g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.439-720T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010093 | |||||||
chr6:167010165 | G | A | 1 | a0001c0001t0073g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.439-648G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010165 | |||||||
chr6:167010169 | A | T | 1 | a0001c0001t0002g0251 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.439-644A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010169 | |||||||
chr6:167010218 | T | G | 1 | a0001c0001t0047g0257 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.439-595T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010218 | |||||||
chr6:167010323 | GA | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.439-482delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 167010323 | ||||||
chr6:167010378 | T | A | 2 | a0001c0001t0028g0074 a0001c0001t0028g0075 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.439-435T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010378 | |||||||
chr6:167010553 | C | T | 43 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(40): Show |
47 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.439-260C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010553 | |||||||
chr6:167010734 | T | C | 1 | a0001c0001t0123g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.439-79T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010734 | |||||||
chr6:167010760 | A | T | 1 | a0001c0001t0026g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.439-53A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010760 | |||||||
chr6:167010762 | A | C | 1 | a0001c0001t0026g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.439-51A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010762 | |||||||
chr6:167010805 | T | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(100): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.439-8T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 5/12 | chr6 | 167010805 | |||||||
chr6:167010906 | T | C | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+13T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167010906 | |||||||
chr6:167011061 | AG | A | 4 | a0001c0001t0001g0016 a0001c0001t0056g0016 a0001c0001t0089g0016 others(1): Show |
4 | HG03486.hp2 NA18987.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+169delG | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011061 | |||||||
chr6:167011062 | G | A | 20 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(17): Show |
21 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.519+169G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011062 | |||||||
chr6:167011063 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+170T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011063 | |||||||
chr6:167011217 | C | T | 3 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.519+324C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011217 | |||||||
chr6:167011256 | AATATT | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+364_519+368del others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011256 | |||||||
chr6:167011289 | G | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+396G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011289 | |||||||
chr6:167011331 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+438A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011331 | |||||||
chr6:167011346 | A | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+453A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011346 | |||||||
chr6:167011349 | C | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+456C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011349 | |||||||
chr6:167011376 | G | A | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+483G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011376 | |||||||
chr6:167011383 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+490T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011383 | |||||||
chr6:167011442 | C | T | 3 | a0001c0001t0068g0172 a0001c0001t0069g0174 a0001c0001t0070g0173 |
3 | HG02615.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.519+549C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011442 | |||||||
chr6:167011469 | GA | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+584delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 167011469 | ||||||
chr6:167011524 | T | G | 1 | a0001c0001t0120g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.519+631T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011524 | |||||||
chr6:167011564 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+671C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011564 | |||||||
chr6:167011698 | G | A | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+805G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011698 | |||||||
chr6:167011779 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.519+886G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011779 | |||||||
chr6:167011787 | G | A | 1 | a0001c0001t0080g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.519+894G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011787 | |||||||
chr6:167011865 | C | T | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.519+972C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011865 | |||||||
chr6:167011872 | C | G | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+979C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167011872 | |||||||
chr6:167012187 | T | G | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+1294T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012187 | |||||||
chr6:167012287 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-1221A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012287 | |||||||
chr6:167012361 | T | C | 7 | a0001c0001t0023g0020 a0001c0001t0023g0218 a0001c0001t0023g0263 others(4): Show |
7 | HG02129.hp1 NA18942.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-1147T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012361 | |||||||
chr6:167012367 | AT | A | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.520-1131delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 167012367 | ||||||
chr6:167012369 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-1139T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012369 | |||||||
chr6:167012407 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-1101A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012407 | |||||||
chr6:167012671 | C | T | 1 | a0001c0001t0181g0121 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.520-837C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012671 | |||||||
chr6:167012843 | C | T | 1 | a0001c0001t0209g0120 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.520-665C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012843 | |||||||
chr6:167012924 | G | T | 1 | a0001c0001t0012g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.520-584G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012924 | |||||||
chr6:167012947 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-561A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012947 | |||||||
chr6:167012950 | A | G | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(100): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-558A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167012950 | |||||||
chr6:167013052 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-456C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013052 | |||||||
chr6:167013074 | C | T | 27 | a0001c0001t0020g0054 a0001c0001t0020g0056 a0001c0001t0020g0063 others(24): Show |
27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.520-434C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013074 | |||||||
chr6:167013111 | C | G | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.520-397C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013111 | |||||||
chr6:167013144 | A | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0028 others(25): Show |
33 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.520-364A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013144 | |||||||
chr6:167013150 | G | A | 3 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.520-358G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013150 | |||||||
chr6:167013187 | C | T | 3 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0067g0167 |
3 | HG01884.hp1 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.520-321C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013187 | |||||||
chr6:167013193 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0017g0011 a0001c0001t0024g0011 others(1): Show |
5 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-315A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013193 | |||||||
chr6:167013219 | T | C | 103 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(100): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.520-289T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013219 | |||||||
chr6:167013382 | A | C | 2 | a0001c0001t0025g0227 a0001c0001t0025g0250 |
2 | NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.520-126A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 6/12 | chr6 | 167013382 | |||||||
chr6:167013592 | A | G | 1 | a0001c0001t0003g0044 | 2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.579+25A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013592 | |||||||
chr6:167013744 | C | T | 29 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(26): Show |
35 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.579+177C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013744 | |||||||
chr6:167013843 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+276T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013843 | |||||||
chr6:167013846 | G | A | 2 | a0001c0001t0024g0215 a0001c0001t0024g0230 |
2 | HG02135.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.579+279G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013846 | |||||||
chr6:167013871 | G | T | 4 | a0001c0001t0003g0226 a0001c0001t0022g0249 a0001c0001t0045g0247 others(1): Show |
4 | HG01261.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+304G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013871 | |||||||
chr6:167013890 | T | C | 1 | a0002c0002t0092g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.579+323T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013890 | |||||||
chr6:167013990 | C | T | 22 | a0001c0001t0039g0064 a0002c0002t0015g0010 a0002c0002t0015g0040 others(19): Show |
23 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.579+423C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167013990 | |||||||
chr6:167014281 | T | G | 2 | a0001c0001t0026g0157 a0001c0001t0026g0158 |
2 | HG01123.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.579+714T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014281 | |||||||
chr6:167014291 | A | G | 1 | a0001c0001t0075g0182 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.579+724A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014291 | |||||||
chr6:167014357 | A | G | 4 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+790A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014357 | |||||||
chr6:167014430 | C | T | 18 | a0001c0001t0010g0002 a0001c0001t0010g0033 a0001c0001t0010g0034 others(15): Show |
20 | HG00408.hp1 HG00621.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+863C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014430 | |||||||
chr6:167014477 | C | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+910C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014477 | |||||||
chr6:167014726 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+1159T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167014726 | |||||||
chr6:167015034 | C | G | 1 | a0001c0001t0037g0136 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.579+1467C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015034 | |||||||
chr6:167015099 | C | T | 11 | a0001c0001t0043g0030 a0001c0001t0048g0004 a0001c0001t0049g0154 others(8): Show |
13 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+1532C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015099 | |||||||
chr6:167015136 | T | G | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.579+1569T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015136 | |||||||
chr6:167015160 | GT | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+1594delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015160 | |||||||
chr6:167015523 | G | A | 1 | a0001c0001t0156g0163 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.579+1956G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015523 | |||||||
chr6:167015542 | A | G | 1 | a0001c0001t0033g0181 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.579+1975A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015542 | |||||||
chr6:167015590 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+2023G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015590 | |||||||
chr6:167015627 | C | T | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+2060C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015627 | |||||||
chr6:167015629 | G | C | 1 | a0001c0001t0172g0255 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.579+2062G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015629 | |||||||
chr6:167015815 | CT | C | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.579+2249delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015815 | |||||||
chr6:167015943 | G | A | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+2376G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015943 | |||||||
chr6:167015979 | A | G | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.579+2412A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167015979 | |||||||
chr6:167016090 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+2523A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016090 | |||||||
chr6:167016403 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+2836C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016403 | |||||||
chr6:167016591 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+3024T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016591 | |||||||
chr6:167016633 | A | G | 1 | a0004c0004t0038g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.579+3066A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016633 | |||||||
chr6:167016698 | A | G | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.579+3131A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016698 | |||||||
chr6:167016816 | G | A | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+3249G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016816 | |||||||
chr6:167016849 | G | GGGT | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+3284_579+3286d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167016849 | ||||||
chr6:167016978 | T | A | 17 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0035g0200 others(14): Show |
18 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+3411T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016978 | |||||||
chr6:167016979 | A | T | 17 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0035g0200 others(14): Show |
18 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+3412A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016979 | |||||||
chr6:167016990 | AT | A | 8 | a0001c0001t0020g0054 a0001c0001t0042g0061 a0001c0001t0042g0062 others(5): Show |
8 | HG02738.hp1 HG02970.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3438delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167016990 | ||||||
chr6:167016994 | T | A | 315 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(312): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.579+3427T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016994 | |||||||
chr6:167016995 | T | A | 3 | a0001c0001t0020g0054 a0001c0001t0121g0053 a0001c0001t0123g0070 |
3 | HG03704.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.579+3428T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016995 | |||||||
chr6:167016998 | T | A | 182 | a0001c0001t0001g0100 a0001c0001t0002g0006 a0001c0001t0002g0007 others(179): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.579+3431T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167016998 | |||||||
chr6:167017002 | T | A | 24 | a0001c0001t0060g0076 a0001c0001t0068g0172 a0001c0001t0070g0173 others(21): Show |
25 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+3435T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017002 | |||||||
chr6:167017022 | GTC | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+3463_579+3464d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167017022 | ||||||
chr6:167017064 | C | T | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3497C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017064 | |||||||
chr6:167017172 | T | A | 1 | a0001c0001t0054g0027 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.579+3605T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017172 | |||||||
chr6:167017174 | T | G | 1 | a0001c0001t0059g0102 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.579+3607T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017174 | |||||||
chr6:167017205 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+3638T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017205 | |||||||
chr6:167017216 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+3649T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017216 | |||||||
chr6:167017296 | A | G | 1 | a0005c0005t0074g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.579+3729A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017296 | |||||||
chr6:167017545 | T | G | 3 | a0001c0001t0068g0172 a0001c0001t0069g0174 a0001c0001t0070g0173 |
3 | HG02615.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.579+3978T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017545 | |||||||
chr6:167017548 | T | TTGAC | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+3984_579+3985i others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167017548 | ||||||
chr6:167017584 | TTC | T | 9 | a0001c0001t0004g0012 a0001c0001t0004g0079 a0001c0001t0004g0080 others(6): Show |
9 | HG00544.hp2 HG02083.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+4019_579+4020d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167017584 | ||||||
chr6:167017586 | C | CT | 24 | a0001c0001t0005g0225 a0001c0001t0007g0171 a0001c0001t0181g0121 others(21): Show |
25 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+4033dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167017586 | ||||||
chr6:167017586 | C | T | 1 | a0001c0001t0016g0081 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.579+4019C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017586 | |||||||
chr6:167017659 | C | T | 131 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.579+4092C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017659 | |||||||
chr6:167017838 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+4271C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017838 | |||||||
chr6:167017839 | G | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+4272G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017839 | |||||||
chr6:167017975 | CAT | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+4409_579+4410d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167017975 | |||||||
chr6:167018021 | G | A | 1 | a0001c0001t0132g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.580-4388G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018021 | |||||||
chr6:167018084 | G | T | 1 | a0002c0002t0101g0205 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.580-4325G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018084 | |||||||
chr6:167018102 | C | T | 12 | a0001c0001t0011g0008 a0001c0001t0011g0026 a0001c0001t0011g0031 others(9): Show |
13 | HG01168.hp1 HG01256.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-4307C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018102 | |||||||
chr6:167018125 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-4284A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018125 | |||||||
chr6:167018153 | C | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-4256C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018153 | |||||||
chr6:167018236 | A | T | 1 | a0001c0001t0020g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.580-4173A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018236 | |||||||
chr6:167018316 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-4093T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018316 | |||||||
chr6:167018341 | T | C | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.580-4068T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018341 | |||||||
chr6:167018394 | T | C | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-4015T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018394 | |||||||
chr6:167018422 | G | A | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.580-3987G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018422 | |||||||
chr6:167018450 | CG | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-3957delG | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167018450 | ||||||
chr6:167018461 | G | A | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.580-3948G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018461 | |||||||
chr6:167018486 | G | C | 1 | a0001c0001t0131g0071 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-3923G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018486 | |||||||
chr6:167018548 | A | G | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.580-3861A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018548 | |||||||
chr6:167018665 | C | T | 7 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(4): Show |
7 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-3744C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018665 | |||||||
chr6:167018774 | C | T | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-3635C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018774 | |||||||
chr6:167018900 | T | C | 44 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(41): Show |
48 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.580-3509T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018900 | |||||||
chr6:167018916 | T | G | 4 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0074g0208 others(1): Show |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-3493T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167018916 | |||||||
chr6:167019053 | C | T | 1 | a0001c0001t0021g0097 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.580-3356C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019053 | |||||||
chr6:167019145 | G | T | 1 | a0001c0001t0072g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.580-3264G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019145 | |||||||
chr6:167019160 | G | A | 1 | a0001c0001t0146g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.580-3249G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019160 | |||||||
chr6:167019235 | T | C | 3 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0088g0210 |
4 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-3174T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019235 | |||||||
chr6:167019257 | GCATACAC others(14): Show |
G | 23 | a0001c0001t0020g0054 a0001c0001t0020g0063 a0002c0002t0015g0010 others(20): Show |
24 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.580-3131_580-3111d others(23): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167019257 | ||||||
chr6:167019272 | G | A | 5 | a0004c0004t0038g0098 a0004c0004t0039g0093 a0004c0004t0109g0023 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-3137G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019272 | |||||||
chr6:167019278 | A | G | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.580-3131A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019278 | |||||||
chr6:167019278 | ACATACAC others(14): Show |
A | 1 | a0001c0001t0016g0081 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.580-3129_580-3109d others(23): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167019278 | ||||||
chr6:167019280 | A | ATACACCT others(14): Show |
7 | a0001c0001t0023g0020 a0001c0001t0023g0218 a0001c0001t0023g0263 others(4): Show |
7 | HG02129.hp1 NA18942.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-3109_580-3089d others(23): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167019280 | ||||||
chr6:167019280 | A | G | 91 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(88): Show |
102 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.580-3129A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019280 | |||||||
chr6:167019301 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-3108G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019301 | |||||||
chr6:167019321 | G | C | 1 | a0001c0001t0016g0081 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.580-3088G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019321 | |||||||
chr6:167019368 | G | A | 1 | a0002c0002t0092g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.580-3041G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019368 | |||||||
chr6:167019565 | A | G | 1 | a0001c0001t0029g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.580-2844A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019565 | |||||||
chr6:167019704 | A | G | 1 | a0002c0002t0097g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.580-2705A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019704 | |||||||
chr6:167019819 | G | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-2590G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019819 | |||||||
chr6:167019832 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-2577A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167019832 | |||||||
chr6:167020007 | A | G | 1 | a0001c0001t0147g0245 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.580-2402A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020007 | |||||||
chr6:167020055 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-2354C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020055 | |||||||
chr6:167020241 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-2168C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020241 | |||||||
chr6:167020335 | A | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-2074A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020335 | |||||||
chr6:167020357 | T | G | 1 | a0002c0002t0097g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.580-2052T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020357 | |||||||
chr6:167020379 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-2030A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020379 | |||||||
chr6:167020428 | C | T | 1 | a0001c0001t0070g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.580-1981C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020428 | |||||||
chr6:167020437 | G | A | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.580-1972G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020437 | |||||||
chr6:167020450 | C | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-1959C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020450 | |||||||
chr6:167020460 | T | C | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.580-1949T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020460 | |||||||
chr6:167020624 | A | G | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.580-1785A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020624 | |||||||
chr6:167020640 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-1769G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020640 | |||||||
chr6:167020646 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-1763C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020646 | |||||||
chr6:167020647 | G | A | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.580-1762G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020647 | |||||||
chr6:167020715 | C | T | 97 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(94): Show |
110 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.580-1694C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020715 | |||||||
chr6:167020754 | C | T | 7 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(4): Show |
7 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1655C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020754 | |||||||
chr6:167020782 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-1627G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020782 | |||||||
chr6:167020823 | C | T | 1 | a0001c0001t0042g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.580-1586C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167020823 | |||||||
chr6:167020908 | CA | C | 139 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(136): Show |
152 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.580-1477delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167020908 | ||||||
chr6:167020908 | CAAA | C | 26 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(23): Show |
30 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.580-1479_580-1477d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167020908 | ||||||
chr6:167020908 | CAAAA | C | 9 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(6): Show |
10 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-1480_580-1477d others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167020908 | ||||||
chr6:167020908 | CAAAAA | C | 113 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(110): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.580-1481_580-1477d others(7): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167020908 | ||||||
chr6:167020908 | CAAAAAA | C | 8 | a0001c0001t0084g0275 a0001c0001t0155g0248 a0003c0003t0009g0037 others(5): Show |
10 | HG01109.hp1 HG01993.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-1482_580-1477d others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167020908 | ||||||
chr6:167021072 | GA | G | 212 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(209): Show |
234 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.580-1323delA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167021072 | ||||||
chr6:167021072 | GAA | G | 18 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0071g0192 others(15): Show |
21 | HG01109.hp1 HG02109.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.580-1324_580-1323d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167021072 | ||||||
chr6:167021072 | GAAAAAA | G | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.580-1328_580-1323d others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167021072 | ||||||
chr6:167021075 | A | G | 1 | a0004c0004t0038g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.580-1334A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021075 | |||||||
chr6:167021118 | A | G | 2 | a0001c0001t0027g0018 a0001c0001t0062g0018 |
3 | HG00099.hp2 HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.580-1291A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021118 | |||||||
chr6:167021166 | G | A | 1 | a0004c0004t0038g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.580-1243G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021166 | |||||||
chr6:167021198 | T | C | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.580-1211T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021198 | |||||||
chr6:167021291 | C | G | 1 | a0001c0001t0072g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.580-1118C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021291 | |||||||
chr6:167021544 | C | T | 1 | a0001c0001t0023g0263 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.580-865C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021544 | |||||||
chr6:167021552 | G | A | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-857G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021552 | |||||||
chr6:167021570 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-839C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021570 | |||||||
chr6:167021573 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0005g0045 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.580-836G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021573 | |||||||
chr6:167021589 | G | A | 7 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(4): Show |
9 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-820G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021589 | |||||||
chr6:167021599 | G | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
108 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.580-810G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021599 | |||||||
chr6:167021715 | T | TAC | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-679_580-678dup others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167021715 | ||||||
chr6:167021715 | TAC | T | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-679_580-678del others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167021715 | ||||||
chr6:167021740 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.580-669G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021740 | |||||||
chr6:167021837 | T | C | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.580-572T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167021837 | |||||||
chr6:167022094 | T | C | 7 | a0001c0001t0003g0044 a0001c0001t0003g0220 a0001c0001t0003g0232 others(4): Show |
8 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-315T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | chr6 | 167022094 | |||||||
chr6:167022259 | A | AAC | 127 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(124): Show |
142 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.580-114_580-113dup others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACAC | 34 | a0001c0001t0001g0124 a0001c0001t0004g0012 a0001c0001t0004g0080 others(31): Show |
35 | HG00673.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.580-116_580-113dup others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACACAC | 7 | a0001c0001t0014g0123 a0001c0001t0020g0063 a0001c0001t0042g0061 others(4): Show |
8 | HG01515.hp2 HG01517.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-118_580-113dup others(6): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACACACA others(1): Show |
5 | a0001c0001t0042g0062 a0001c0001t0061g0066 a0001c0001t0104g0058 others(2): Show |
5 | HG02717.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-120_580-113dup others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACACACA others(3): Show |
14 | a0002c0002t0015g0010 a0002c0002t0015g0206 a0002c0002t0036g0010 others(11): Show |
16 | HG00609.hp1 HG02080.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-122_580-113dup others(10): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACACACA others(5): Show |
6 | a0002c0002t0015g0040 a0002c0002t0035g0200 a0002c0002t0036g0202 others(3): Show |
6 | HG00621.hp2 HG01361.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-124_580-113dup others(12): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | A | AACACACA others(7): Show |
2 | a0002c0002t0035g0203 a0006c0007t0090g0194 |
2 | HG00597.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.580-126_580-113dup others(14): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | AAC | A | 35 | a0001c0001t0001g0151 a0001c0001t0006g0234 a0001c0001t0006g0252 others(32): Show |
39 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.580-114_580-113del others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022259 | AACAC | A | 12 | a0001c0001t0002g0233 a0001c0001t0013g0137 a0001c0001t0039g0064 others(9): Show |
14 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-116_580-113del others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022259 | ||||||
chr6:167022310 | C | CACAA | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.580-96_580-95insAA others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 167022310 | ||||||
chr6:167022671 | T | C | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(94): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.806+36T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167022671 | |||||||
chr6:167022828 | C | A | 2 | a0001c0001t0020g0054 a0001c0001t0020g0063 |
2 | HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.806+193C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167022828 | |||||||
chr6:167022882 | G | C | 3 | a0001c0001t0040g0025 a0001c0001t0110g0161 a0001c0001t0115g0025 |
3 | HG01099.hp2 HG01243.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.806+247G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167022882 | |||||||
chr6:167022893 | A | G | 1 | a0001c0001t0069g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.806+258A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167022893 | |||||||
chr6:167022973 | T | C | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(94): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.806+338T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167022973 | |||||||
chr6:167023010 | C | T | 7 | a0001c0001t0200g0128 a0003c0003t0009g0037 a0003c0003t0009g0038 others(4): Show |
9 | HG00741.hp2 HG01109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+375C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023010 | |||||||
chr6:167023014 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.806+379T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023014 | |||||||
chr6:167023048 | A | G | 3 | a0001c0001t0127g0052 a0001c0001t0129g0021 a0001c0001t0130g0021 |
3 | HG01243.hp1 HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.806+413A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023048 | |||||||
chr6:167023092 | T | C | 11 | a0001c0001t0043g0030 a0001c0001t0048g0004 a0001c0001t0049g0154 others(8): Show |
13 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+457T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023092 | |||||||
chr6:167023093 | A | T | 11 | a0001c0001t0043g0030 a0001c0001t0048g0004 a0001c0001t0049g0154 others(8): Show |
13 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+458A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023093 | |||||||
chr6:167023124 | G | A | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.806+489G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023124 | |||||||
chr6:167023144 | C | T | 43 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(40): Show |
47 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.806+509C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023144 | |||||||
chr6:167023213 | G | T | 4 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+578G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023213 | |||||||
chr6:167023387 | C | T | 11 | a0001c0001t0043g0030 a0001c0001t0048g0004 a0001c0001t0049g0154 others(8): Show |
13 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+752C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023387 | |||||||
chr6:167023392 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.806+757T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023392 | |||||||
chr6:167023520 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.806+885T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023520 | |||||||
chr6:167023638 | G | T | 38 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(35): Show |
45 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.806+1003G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023638 | |||||||
chr6:167023674 | T | A | 110 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(107): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.806+1039T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023674 | |||||||
chr6:167023879 | C | T | 1 | a0001c0001t0112g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.807-903C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167023879 | |||||||
chr6:167024002 | TAAC | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.807-778_807-776del others(3): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 167024002 | ||||||
chr6:167024315 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.807-467C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024315 | |||||||
chr6:167024332 | G | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(94): Show |
110 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.807-450G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024332 | |||||||
chr6:167024357 | T | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-425T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024357 | |||||||
chr6:167024415 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.807-367A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024415 | |||||||
chr6:167024500 | C | T | 131 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.807-282C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024500 | |||||||
chr6:167024577 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.807-205G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024577 | |||||||
chr6:167024755 | C | T | 1 | a0001c0001t0073g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.807-27C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 8/12 | chr6 | 167024755 | |||||||
chr6:167024910 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+16T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167024910 | |||||||
chr6:167024952 | C | T | 1 | a0001c0001t0204g0085 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.919+58C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167024952 | |||||||
chr6:167024971 | T | G | 2 | a0001c0001t0071g0192 a0001c0001t0072g0193 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.919+77T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167024971 | |||||||
chr6:167024977 | T | C | 5 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(2): Show |
5 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+83T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167024977 | |||||||
chr6:167025002 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+108T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025002 | |||||||
chr6:167025061 | A | G | 1 | a0001c0001t0104g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.919+167A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025061 | |||||||
chr6:167025123 | G | A | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.919+229G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025123 | |||||||
chr6:167025215 | T | G | 1 | a0002c0002t0103g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919+321T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025215 | |||||||
chr6:167025216 | G | A | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+322G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025216 | |||||||
chr6:167025268 | A | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+374A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025268 | |||||||
chr6:167025342 | C | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+448C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025342 | |||||||
chr6:167025427 | C | T | 1 | a0001c0001t0013g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.919+533C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025427 | |||||||
chr6:167025545 | A | C | 1 | a0001c0001t0011g0132 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.919+651A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025545 | |||||||
chr6:167025623 | C | T | 1 | a0001c0001t0150g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.919+729C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025623 | |||||||
chr6:167025677 | A | T | 1 | a0001c0001t0026g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.919+783A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025677 | |||||||
chr6:167025978 | A | G | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.920-569A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167025978 | |||||||
chr6:167026058 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-489T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026058 | |||||||
chr6:167026060 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-487G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026060 | |||||||
chr6:167026288 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-259A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026288 | |||||||
chr6:167026344 | C | CAG | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-202_920-201dup others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 167026344 | ||||||
chr6:167026355 | C | T | 1 | a0001c0001t0012g0029 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.920-192C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026355 | |||||||
chr6:167026359 | G | A | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-188G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026359 | |||||||
chr6:167026398 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-149A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026398 | |||||||
chr6:167026421 | T | C | 2 | a0001c0001t0042g0061 a0001c0001t0042g0062 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.920-126T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026421 | |||||||
chr6:167026472 | C | T | 2 | a0001c0001t0086g0180 a0001c0001t0125g0060 |
2 | HG02738.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.920-75C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 9/12 | chr6 | 167026472 | |||||||
chr6:167026640 | C | T | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.988+25C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167026640 | |||||||
chr6:167026646 | G | A | 1 | a0001c0001t0132g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.988+31G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167026646 | |||||||
chr6:167026756 | T | C | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.988+141T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167026756 | |||||||
chr6:167026871 | G | T | 1 | a0001c0001t0188g0150 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.988+256G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167026871 | |||||||
chr6:167027013 | C | G | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+398C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027013 | |||||||
chr6:167027014 | A | T | 4 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | HG02040.hp1 HG02129.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+399A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027014 | |||||||
chr6:167027070 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.988+455G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027070 | |||||||
chr6:167027077 | C | G | 1 | a0001c0001t0046g0273 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.988+462C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027077 | |||||||
chr6:167027079 | A | G | 3 | a0001c0001t0044g0032 a0001c0001t0137g0022 a0001c0001t0139g0022 |
4 | HG00099.hp1 HG02523.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+464A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027079 | |||||||
chr6:167027130 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+515G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027130 | |||||||
chr6:167027248 | G | A | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+633G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027248 | |||||||
chr6:167027268 | C | T | 2 | a0001c0001t0042g0061 a0001c0001t0042g0062 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.988+653C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027268 | |||||||
chr6:167027291 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+676T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027291 | |||||||
chr6:167027433 | CTG | C | 3 | a0001c0001t0002g0237 a0001c0001t0005g0042 a0001c0001t0170g0042 |
3 | NA18978.hp1 NA19003.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.988+821_988+822del others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 167027433 | ||||||
chr6:167027472 | T | TCA | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+860_988+861dup others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 167027472 | ||||||
chr6:167027535 | T | G | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+920T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027535 | |||||||
chr6:167027704 | A | G | 1 | a0002c0002t0101g0205 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.988+1089A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027704 | |||||||
chr6:167027906 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1291G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027906 | |||||||
chr6:167027968 | G | A | 2 | a0001c0001t0202g0110 a0001c0001t0215g0152 |
2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.988+1353G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167027968 | |||||||
chr6:167028055 | T | TA | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1441dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 167028055 | ||||||
chr6:167028081 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1466G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028081 | |||||||
chr6:167028136 | T | C | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.988+1521T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028136 | |||||||
chr6:167028236 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1621C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028236 | |||||||
chr6:167028386 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1771T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028386 | |||||||
chr6:167028411 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+1796T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028411 | |||||||
chr6:167028619 | G | A | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.988+2004G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028619 | |||||||
chr6:167028627 | C | T | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.988+2012C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028627 | |||||||
chr6:167028707 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+2092G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028707 | |||||||
chr6:167028808 | T | C | 1 | a0001c0001t0107g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.988+2193T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028808 | |||||||
chr6:167028903 | A | C | 1 | a0001c0001t0171g0216 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.988+2288A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167028903 | |||||||
chr6:167029036 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+2421T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029036 | |||||||
chr6:167029037 | G | T | 1 | a0001c0001t0177g0268 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.988+2422G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029037 | |||||||
chr6:167029055 | C | T | 25 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(22): Show |
29 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.988+2440C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029055 | |||||||
chr6:167029067 | GTGTTTTT others(1): Show |
G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+2469_988+2476d others(10): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 167029067 | ||||||
chr6:167029149 | C | T | 1 | a0001c0001t0118g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.988+2534C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029149 | |||||||
chr6:167029461 | A | G | 1 | a0001c0001t0190g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.988+2846A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029461 | |||||||
chr6:167029495 | A | G | 2 | a0001c0001t0118g0072 a0001c0001t0131g0071 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.988+2880A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029495 | |||||||
chr6:167029500 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+2885T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029500 | |||||||
chr6:167029506 | C | A | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+2891C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029506 | |||||||
chr6:167029507 | C | G | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+2892C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029507 | |||||||
chr6:167029529 | T | C | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.988+2914T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029529 | |||||||
chr6:167029575 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.988+2960G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029575 | |||||||
chr6:167029876 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-2727T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029876 | |||||||
chr6:167029884 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-2719T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029884 | |||||||
chr6:167029914 | C | T | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.989-2689C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029914 | |||||||
chr6:167029935 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-2668A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029935 | |||||||
chr6:167029955 | C | T | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.989-2648C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029955 | |||||||
chr6:167029968 | G | T | 13 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(10): Show |
16 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.989-2635G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029968 | |||||||
chr6:167029987 | A | G | 1 | a0001c0001t0121g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.989-2616A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167029987 | |||||||
chr6:167030216 | C | T | 1 | a0001c0001t0060g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.989-2387C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030216 | |||||||
chr6:167030217 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0159g0048 |
2 | NA18612.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.989-2386C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030217 | |||||||
chr6:167030234 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-2369C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030234 | |||||||
chr6:167030414 | C | T | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.989-2189C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030414 | |||||||
chr6:167030430 | T | C | 5 | a0001c0001t0006g0219 a0001c0001t0006g0234 a0001c0001t0006g0252 others(2): Show |
5 | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-2173T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030430 | |||||||
chr6:167030482 | C | T | 1 | a0001c0001t0132g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.989-2121C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030482 | |||||||
chr6:167030601 | T | C | 43 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(40): Show |
47 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.989-2002T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030601 | |||||||
chr6:167030672 | G | T | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.989-1931G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030672 | |||||||
chr6:167030685 | C | A | 1 | a0001c0001t0180g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.989-1918C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030685 | |||||||
chr6:167030722 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-1881C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030722 | |||||||
chr6:167030766 | T | C | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.989-1837T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030766 | |||||||
chr6:167030793 | C | T | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.989-1810C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030793 | |||||||
chr6:167030802 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-1801A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030802 | |||||||
chr6:167030867 | CTTTGT | C | 131 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.989-1735_989-1731d others(7): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030867 | |||||||
chr6:167030874 | C | G | 131 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.989-1729C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030874 | |||||||
chr6:167030876 | A | C | 131 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(128): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.989-1727A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030876 | |||||||
chr6:167030935 | C | T | 1 | a0001c0001t0073g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.989-1668C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167030935 | |||||||
chr6:167031205 | G | A | 1 | a0001c0001t0003g0238 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.989-1398G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031205 | |||||||
chr6:167031242 | A | T | 6 | a0001c0001t0002g0045 a0001c0001t0002g0047 a0001c0001t0002g0241 others(3): Show |
6 | HG02630.hp2 HG02647.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.989-1361A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031242 | |||||||
chr6:167031341 | G | A | 1 | a0001c0001t0022g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.989-1262G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031341 | |||||||
chr6:167031390 | A | G | 2 | a0001c0001t0151g0270 a0001c0001t0179g0269 |
2 | NA18940.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.989-1213A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031390 | |||||||
chr6:167031409 | G | T | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-1194G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031409 | |||||||
chr6:167031449 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-1154G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031449 | |||||||
chr6:167031545 | A | G | 1 | a0001c0001t0117g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.989-1058A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031545 | |||||||
chr6:167031651 | T | C | 46 | a0001c0001t0008g0019 a0001c0001t0008g0035 a0001c0001t0008g0186 others(43): Show |
51 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.989-952T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031651 | |||||||
chr6:167031659 | C | G | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-944C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031659 | |||||||
chr6:167031726 | C | T | 1 | a0001c0001t0172g0255 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.989-877C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031726 | |||||||
chr6:167031798 | A | G | 2 | a0001c0001t0060g0076 a0001c0001t0063g0077 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.989-805A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031798 | |||||||
chr6:167031835 | T | G | 1 | a0001c0001t0007g0176 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.989-768T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031835 | |||||||
chr6:167031839 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0028 others(18): Show |
26 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.989-764A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031839 | |||||||
chr6:167031842 | T | C | 3 | a0001c0001t0118g0072 a0001c0001t0120g0073 a0001c0001t0131g0071 |
3 | HG02572.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.989-761T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031842 | |||||||
chr6:167031944 | A | G | 3 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989-659A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167031944 | |||||||
chr6:167032003 | C | T | 17 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(14): Show |
18 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.989-600C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032003 | |||||||
chr6:167032034 | G | GA | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-568dupA | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 167032034 | ||||||
chr6:167032106 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-497A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032106 | |||||||
chr6:167032319 | G | A | 1 | a0001c0001t0192g0133 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.989-284G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032319 | |||||||
chr6:167032446 | A | G | 1 | a0001c0001t0013g0137 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.989-157A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032446 | |||||||
chr6:167032519 | A | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.989-84A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032519 | |||||||
chr6:167032575 | A | G | 1 | a0001c0001t0215g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.989-28A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 10/12 | chr6 | 167032575 | |||||||
chr6:167032699 | C | T | 1 | a0001c0001t0073g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1028+57C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032699 | |||||||
chr6:167032700 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1028+58G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032700 | |||||||
chr6:167032709 | CAA | C | 3 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 |
3 | HG02486.hp1 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1028+68_1028+69del others(2): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032709 | |||||||
chr6:167032853 | T | A | 1 | a0001c0001t0013g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1028+211T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032853 | |||||||
chr6:167032939 | G | A | 3 | a0001c0001t0002g0237 a0001c0001t0005g0042 a0001c0001t0170g0042 |
3 | NA18978.hp1 NA19003.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1028+297G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032939 | |||||||
chr6:167032970 | A | G | 4 | a0005c0005t0019g0041 a0005c0005t0019g0209 a0005c0005t0074g0208 others(1): Show |
5 | HG02109.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1028+328A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167032970 | |||||||
chr6:167033083 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1028+441A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033083 | |||||||
chr6:167033099 | C | CT | 10 | a0001c0001t0008g0019 a0001c0001t0010g0034 a0001c0001t0013g0101 others(7): Show |
11 | HG02027.hp2 HG02486.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028+486dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CT | C | 50 | a0001c0001t0001g0028 a0001c0001t0001g0103 a0001c0001t0001g0106 others(47): Show |
52 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1028+486delT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CTT | C | 211 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(208): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1028+485_1028+486d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CTTT | C | 13 | a0001c0001t0002g0214 a0001c0001t0002g0241 a0001c0001t0002g0264 others(10): Show |
13 | HG01256.hp1 HG02004.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1028+484_1028+486d others(5): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CTTTTTT | C | 18 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(15): Show |
19 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1028+481_1028+486d others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0116g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1028+476_1028+486d others(13): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033099 | CTTTTTTT others(7): Show |
C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+473_1028+486d others(16): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 167033099 | ||||||
chr6:167033183 | T | C | 1 | a0001c0001t0004g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1028+541T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033183 | |||||||
chr6:167033247 | A | C | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1028+605A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033247 | |||||||
chr6:167033300 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1029-575A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033300 | |||||||
chr6:167033301 | G | A | 1 | a0001c0001t0004g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1029-574G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033301 | |||||||
chr6:167033310 | C | T | 13 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(10): Show |
16 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-565C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033310 | |||||||
chr6:167033371 | A | C | 18 | a0001c0001t0010g0002 a0001c0001t0010g0033 a0001c0001t0010g0034 others(15): Show |
20 | HG00408.hp1 HG00621.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1029-504A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033371 | |||||||
chr6:167033445 | G | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1029-430G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033445 | |||||||
chr6:167033668 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1029-207C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 11/12 | chr6 | 167033668 | |||||||
chr6:167034269 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+298T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034269 | |||||||
chr6:167034401 | A | G | 2 | a0001c0001t0176g0267 a0001c0001t0177g0268 |
2 | NA18973.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1125+430A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034401 | |||||||
chr6:167034483 | A | G | 1 | a0001c0001t0132g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1125+512A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034483 | |||||||
chr6:167034625 | T | A | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1125+654T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034625 | |||||||
chr6:167034643 | G | A | 1 | a0001c0001t0031g0185 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1125+672G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034643 | |||||||
chr6:167034673 | TGA | T | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1125+708_1125+709d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167034673 | ||||||
chr6:167034693 | A | G | 109 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1125+722A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034693 | |||||||
chr6:167034751 | A | G | 7 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(4): Show |
8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1125+780A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034751 | |||||||
chr6:167034780 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+809T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034780 | |||||||
chr6:167034885 | TTA | T | 130 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(127): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1125+919_1125+920d others(4): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167034885 | ||||||
chr6:167034967 | A | C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0214 a0001c0001t0002g0251 others(2): Show |
5 | HG00408.hp2 NA18951.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125+996A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167034967 | |||||||
chr6:167035108 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+1137C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035108 | |||||||
chr6:167035240 | C | T | 93 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(90): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1125+1269C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035240 | |||||||
chr6:167035254 | G | A | 1 | a0001c0001t0073g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1125+1283G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035254 | |||||||
chr6:167035309 | C | T | 1 | a0001c0001t0213g0114 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1125+1338C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035309 | |||||||
chr6:167035571 | G | GT | 33 | a0001c0001t0003g0253 a0001c0001t0010g0178 a0001c0001t0076g0179 others(30): Show |
36 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1125+1614dupT | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167035571 | ||||||
chr6:167035571 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1125+1600G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035571 | |||||||
chr6:167035599 | C | T | 3 | a0001c0001t0118g0072 a0001c0001t0120g0073 a0001c0001t0131g0071 |
3 | HG02572.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1125+1628C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035599 | |||||||
chr6:167035628 | G | A | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1125+1657G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035628 | |||||||
chr6:167035693 | C | A | 1 | a0001c0001t0005g0225 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1125+1722C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035693 | |||||||
chr6:167035693 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+1722C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035693 | |||||||
chr6:167035729 | G | C | 2 | a0001c0001t0028g0074 a0001c0001t0028g0075 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1125+1758G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035729 | |||||||
chr6:167035732 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+1761G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035732 | |||||||
chr6:167035858 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1125+1887C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035858 | |||||||
chr6:167035959 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+1988G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035959 | |||||||
chr6:167035977 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+2006C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167035977 | |||||||
chr6:167036144 | A | G | 2 | a0002c0002t0093g0201 a0002c0002t0096g0199 |
2 | HG02080.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1125+2173A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036144 | |||||||
chr6:167036267 | T | C | 1 | a0001c0001t0126g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1125+2296T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036267 | |||||||
chr6:167036285 | C | A | 4 | a0001c0001t0064g0168 a0001c0001t0065g0165 a0001c0001t0066g0166 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+2314C>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036285 | |||||||
chr6:167036293 | A | G | 27 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(24): Show |
30 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1125+2322A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036293 | |||||||
chr6:167036460 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1125+2489G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036460 | |||||||
chr6:167036530 | T | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+2559T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036530 | |||||||
chr6:167036531 | C | T | 1 | a0001c0001t0168g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1125+2560C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036531 | |||||||
chr6:167036579 | T | G | 1 | a0001c0001t0002g0233 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1125+2608T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036579 | |||||||
chr6:167036683 | C | T | 97 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(94): Show |
110 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1125+2712C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036683 | |||||||
chr6:167036965 | C | T | 26 | a0001c0001t0012g0029 a0001c0001t0020g0054 a0001c0001t0020g0056 others(23): Show |
28 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126-2939C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036965 | |||||||
chr6:167036984 | G | T | 1 | a0001c0001t0004g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1126-2920G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167036984 | |||||||
chr6:167037025 | C | G | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-2879C>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037025 | |||||||
chr6:167037102 | G | A | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-2802G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037102 | |||||||
chr6:167037121 | A | G | 13 | a0001c0001t0071g0192 a0001c0001t0072g0193 a0001c0001t0073g0191 others(10): Show |
16 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1126-2783A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037121 | |||||||
chr6:167037139 | T | A | 13 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(10): Show |
14 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1126-2765T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037139 | |||||||
chr6:167037218 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-2686T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037218 | |||||||
chr6:167037354 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-2550T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037354 | |||||||
chr6:167037357 | CACTCAAT others(1): Show |
C | 45 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0043 others(42): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1126-2543_1126-253 others(12): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167037357 | ||||||
chr6:167037361 | CAATT | C | 32 | a0001c0001t0002g0006 a0001c0001t0002g0046 a0001c0001t0002g0214 others(29): Show |
34 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1126-2541_1126-253 others(8): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167037361 | ||||||
chr6:167037381 | T | C | 1 | a0001c0001t0004g0090 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1126-2523T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037381 | |||||||
chr6:167037403 | T | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-2501T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037403 | |||||||
chr6:167037486 | T | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-2418T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037486 | |||||||
chr6:167037519 | G | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-2385G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037519 | |||||||
chr6:167037641 | T | C | 96 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1126-2263T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037641 | |||||||
chr6:167037658 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-2246C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037658 | |||||||
chr6:167037708 | T | C | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-2196T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037708 | |||||||
chr6:167037823 | A | G | 155 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0011 others(152): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1126-2081A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037823 | |||||||
chr6:167037919 | G | T | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1126-1985G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167037919 | |||||||
chr6:167038038 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1866T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038038 | |||||||
chr6:167038108 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1796T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038108 | |||||||
chr6:167038125 | T | C | 3 | a0001c0001t0029g0274 a0001c0001t0029g0276 a0001c0001t0084g0275 |
3 | HG02258.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1126-1779T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038125 | |||||||
chr6:167038128 | C | T | 1 | a0001c0001t0158g0222 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1126-1776C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038128 | |||||||
chr6:167038218 | G | A | 4 | a0001c0001t0028g0074 a0001c0001t0028g0075 a0001c0001t0060g0076 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-1686G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038218 | |||||||
chr6:167038287 | C | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(92): Show |
108 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1126-1617C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038287 | |||||||
chr6:167038313 | T | TTCAGCCT others(10): Show |
21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1588_1126-158 others(21): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 167038313 | ||||||
chr6:167038342 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1562T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038342 | |||||||
chr6:167038503 | A | G | 1 | a0005c0005t0074g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1126-1401A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038503 | |||||||
chr6:167038541 | A | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1363A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038541 | |||||||
chr6:167038608 | G | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-1296G>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038608 | |||||||
chr6:167038776 | G | A | 1 | a0002c0002t0097g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1126-1128G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038776 | |||||||
chr6:167038925 | A | G | 1 | a0001c0001t0064g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1126-979A>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038925 | |||||||
chr6:167038942 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-962C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038942 | |||||||
chr6:167038945 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-959A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038945 | |||||||
chr6:167038960 | TTTCTCTG others(49): Show |
T | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-943_1126-888d others(58): Show |
CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038960 | |||||||
chr6:167038990 | C | T | 1 | a0001c0001t0068g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1126-914C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167038990 | |||||||
chr6:167039018 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-886T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039018 | |||||||
chr6:167039019 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-885T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039019 | |||||||
chr6:167039031 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-873A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039031 | |||||||
chr6:167039039 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-865G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039039 | |||||||
chr6:167039040 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1126-864A>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039040 | |||||||
chr6:167039046 | T | G | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-858T>G | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039046 | |||||||
chr6:167039085 | A | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-819A>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039085 | |||||||
chr6:167039095 | C | T | 6 | a0003c0003t0009g0037 a0003c0003t0009g0038 a0003c0003t0009g0189 others(3): Show |
8 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-809C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039095 | |||||||
chr6:167039098 | G | A | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-806G>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039098 | |||||||
chr6:167039188 | G | C | 1 | a0001c0001t0209g0120 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1126-716G>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039188 | |||||||
chr6:167039274 | C | T | 29 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0079 others(26): Show |
33 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1126-630C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039274 | |||||||
chr6:167039290 | T | C | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-614T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039290 | |||||||
chr6:167039341 | C | T | 21 | a0002c0002t0015g0010 a0002c0002t0015g0040 a0002c0002t0015g0206 others(18): Show |
22 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1126-563C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039341 | |||||||
chr6:167039472 | T | A | 5 | a0001c0001t0012g0029 a0001c0001t0054g0027 a0001c0001t0183g0142 others(2): Show |
7 | HG00544.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126-432T>A | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039472 | |||||||
chr6:167039541 | C | T | 1 | a0001c0001t0120g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1126-363C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039541 | |||||||
chr6:167039565 | C | T | 3 | a0001c0001t0020g0056 a0001c0001t0113g0057 a0001c0001t0126g0055 |
3 | HG02698.hp2 HG03490.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1126-339C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039565 | |||||||
chr6:167039678 | C | T | 1 | a0001c0001t0189g0125 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1126-226C>T | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039678 | |||||||
chr6:167039757 | T | C | 333 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(330): Show |
363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.1126-147T>C | CEP43 | ENSG00000213066.14 | transcript | ENST00000366847.9 | protein_coding | 12/12 | chr6 | 167039757 |