Item | Value |
---|---|
geneid | 22897 |
ensemblid | ENSG00000110274.16 |
hgncid | 29182 |
symbol | CEP164 |
name | centrosomal protein 164 |
refseq_nuc | NM_014956.5 |
refseq_prot | NP_055771.4 |
ensembl_nuc | ENST00000278935.8 |
ensembl_prot | ENSP00000278935.3 |
mane_status | MANE Select |
chr | chr11 |
start | 117327854 |
end | 117413266 |
strand | + |
ver | v1.2 |
region | chr11:117327854-117413266 |
region5000 | chr11:117322854-117418266 |
regionname0 | CEP164_chr11_117327854_117413266 |
regionname5000 | CEP164_chr11_117322854_117418266 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1460 | 133 | 15 | 27 | 66 | 5 | 18 | 50 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0002 | 0/0 | 1460 | 102 | 21 | 11 | 60 | 4 | 6 | 43 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0003 | 0/0 | 1460 | 62 | 19 | 14 | 18 | 3 | 8 | 15 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0004 | 0/0 | 1460 | 53 | 15 | 10 | 17 | 3 | 8 | 16 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0005 | 0/0 | 1460 | 6 | 0 | 0 | 5 | 0 | 1 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0006 | 0/0 | 1460 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0007 | 0/0 | 1460 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0008 | 0/0 | 1460 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0009 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0010 | 0/0 | 1460 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0011 | 0/0 | 1460 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0012 | 0/0 | 1460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0013 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0014 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0015 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0016 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0017 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0018 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0019 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0020 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0021 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0022 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0023 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0024 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0025 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
a0026 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | MAGRP others(1455): Show |
chr11 | 117322854 | 117418266 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 4380 | 93 | 12 | 21 | 47 | 4 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0001c0005 | 1/1 | 4380 | 35 | 2 | 6 | 15 | 1 | 9 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0001c0013 | 0/0 | 4380 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0001c0026 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0001c0027 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0001c0036 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0002c0001 | 0/0 | 4380 | 101 | 21 | 11 | 59 | 4 | 6 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0002c0038 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0003c0003 | 0/0 | 4380 | 61 | 18 | 14 | 18 | 3 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0003c0022 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0004 | 0/0 | 4380 | 39 | 12 | 7 | 17 | 0 | 3 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0008 | 0/0 | 4380 | 6 | 0 | 2 | 0 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0009 | 0/0 | 4380 | 4 | 1 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0015 | 0/0 | 4380 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0031 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0004c0034 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0005c0007 | 0/0 | 4380 | 6 | 0 | 0 | 5 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0006c0006 | 0/0 | 4380 | 6 | 6 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0007c0010 | 0/0 | 4380 | 4 | 0 | 3 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0008c0011 | 0/0 | 4380 | 3 | 3 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0009c0020 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0009c0021 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0010c0014 | 0/0 | 4380 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0011c0012 | 0/0 | 4380 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0012c0037 | 0/0 | 4380 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0013c0019 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0014c0030 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0015c0029 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0016c0025 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0017c0016 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0018c0039 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0019c0032 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0020c0017 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0021c0033 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0022c0035 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0023c0023 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0024c0028 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0025c0024 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 | ||
a0026c0018 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | ATGGC others(4375): Show |
chr11 | 117322854 | 117418266 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 5629 | 14 | 7 | 4 | 1 | 1 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0002 | 0/0 | 5629 | 69 | 4 | 15 | 39 | 3 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0003 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0004 | 0/0 | 5629 | 4 | 0 | 1 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0005 | 0/0 | 5629 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0022 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0002t0023 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0005t0005 | 1/1 | 5629 | 33 | 1 | 6 | 15 | 1 | 8 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0005t0016 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0005t0025 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0013t0005 | 0/0 | 5629 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0026t0002 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0027t0002 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0001c0036t0005 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0001 | 0/0 | 5629 | 24 | 4 | 4 | 12 | 3 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0002 | 0/0 | 5629 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0003 | 0/0 | 5629 | 69 | 14 | 5 | 44 | 1 | 5 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0004 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0009 | 0/0 | 5629 | 4 | 2 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0001t0024 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0002c0038t0003 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0003c0003t0002 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0003c0003t0004 | 0/0 | 5629 | 48 | 11 | 13 | 15 | 2 | 7 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0003c0003t0005 | 0/0 | 5629 | 8 | 7 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0003c0003t0011 | 0/0 | 5630 | 3 | 0 | 0 | 1 | 1 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5625): Show |
chr11 | 117322854 | 117418266 |
a0003c0003t0017 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0003c0022t0005 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0004t0001 | 0/0 | 5629 | 34 | 11 | 7 | 14 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0004t0010 | 0/0 | 5629 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0004t0015 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0004t0018 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0008t0001 | 0/0 | 5629 | 6 | 0 | 2 | 0 | 0 | 4 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0009t0008 | 0/0 | 5629 | 4 | 1 | 0 | 0 | 2 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0015t0003 | 0/0 | 5629 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0031t0001 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0004c0034t0007 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0005c0007t0006 | 0/0 | 5629 | 6 | 0 | 0 | 5 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0006c0006t0007 | 0/0 | 5629 | 5 | 5 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0006c0006t0008 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0007c0010t0002 | 0/0 | 5629 | 4 | 0 | 3 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0008c0011t0007 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0008c0011t0012 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0009c0020t0014 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5625): Show |
chr11 | 117322854 | 117418266 |
a0009c0021t0019 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0010c0014t0013 | 0/0 | 5629 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0011c0012t0006 | 0/0 | 5629 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0012c0037t0005 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0013c0019t0004 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0014c0030t0021 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0015c0029t0012 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0016c0025t0001 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0017c0016t0004 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0018c0039t0009 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0019c0032t0020 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5625): Show |
chr11 | 117322854 | 117418266 |
a0020c0017t0004 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0021c0033t0001 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0022c0035t0013 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0023c0023t0006 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0024c0028t0004 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0025c0024t0005 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5624): Show |
chr11 | 117322854 | 117418266 |
a0026c0018t0014 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | GTTGC others(5625): Show |
chr11 | 117322854 | 117418266 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0022g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0002t0023g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0005g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0016g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0005t0025g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0013t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0013t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0026t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0027t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0001c0036t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0009g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0001t0024g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0002c0038t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0003t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0003c0022t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0004t0018g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0008t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0009t0008g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0015t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0015t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0031t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0004c0034t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0005c0007t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0006c0006t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0007c0010t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0008c0011t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0009c0020t0014g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0009c0021t0019g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0010c0014t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0010c0014t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0011c0012t0006g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0011c0012t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0012c0037t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0013c0019t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0014c0030t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0015c0029t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0016c0025t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0017c0016t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0018c0039t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0019c0032t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0020c0017t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0021c0033t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0022c0035t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0023c0023t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0024c0028t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0025c0024t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
a0026c0018t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0178 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00099 | hp2 | a0003 | c0003 | t0004 | g0129 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00140 | hp1 | a0003 | c0003 | t0011 | g0126 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00140 | hp2 | a0002 | c0001 | t0003 | g0187 | EUR | GBR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0356 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00280 | hp2 | a0003 | c0003 | t0004 | g0077 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00323 | hp1 | a0004 | c0015 | t0003 | g0028 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0339 | EUR | FIN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00408 | hp1 | a0003 | c0003 | t0004 | g0142 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00408 | hp2 | a0002 | c0001 | t0003 | g0253 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00423 | hp1 | a0002 | c0001 | t0003 | g0192 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00423 | hp2 | a0001 | c0005 | t0005 | g0171 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00438 | hp1 | a0002 | c0001 | t0003 | g0218 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00544 | hp1 | a0002 | c0038 | t0003 | g0199 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00558 | hp2 | a0002 | c0001 | t0003 | g0216 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00597 | hp1 | a0002 | c0001 | t0003 | g0194 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00597 | hp2 | a0005 | c0007 | t0006 | g0259 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00609 | hp2 | a0002 | c0001 | t0003 | g0217 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0354 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00621 | hp2 | a0002 | c0001 | t0003 | g0001 | EAS | CHS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00639 | hp1 | a0003 | c0003 | t0004 | g0224 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0282 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0299 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0072 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00741 | hp1 | a0003 | c0003 | t0004 | g0226 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0056 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01069 | hp1 | a0002 | c0001 | t0003 | g0214 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01069 | hp2 | a0001 | c0002 | t0023 | g0241 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01070 | hp2 | a0002 | c0001 | t0003 | g0185 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01071 | hp1 | a0002 | c0001 | t0003 | g0211 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01071 | hp2 | a0002 | c0001 | t0003 | g0186 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01074 | hp1 | a0002 | c0001 | t0009 | g0190 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01074 | hp2 | a0007 | c0010 | t0002 | g0009 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01081 | hp1 | a0007 | c0010 | t0002 | g0156 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0291 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0292 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01099 | hp2 | a0001 | c0005 | t0005 | g0090 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0059 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01106 | hp2 | a0001 | c0005 | t0005 | g0058 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0281 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01109 | hp2 | a0001 | c0005 | t0005 | g0349 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01167 | hp1 | a0003 | c0003 | t0004 | g0133 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0093 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01168 | hp2 | a0001 | c0005 | t0005 | g0270 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01175 | hp2 | a0002 | c0001 | t0001 | g0094 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01243 | hp1 | a0002 | c0001 | t0009 | g0251 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01243 | hp2 | a0007 | c0010 | t0002 | g0009 | AMR | PUR | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01257 | hp1 | a0004 | c0004 | t0001 | g0296 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01261 | hp2 | a0003 | c0003 | t0005 | g0008 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01346 | hp1 | a0001 | c0005 | t0005 | g0323 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01358 | hp1 | a0003 | c0003 | t0004 | g0055 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01358 | hp2 | a0004 | c0004 | t0001 | g0326 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01361 | hp2 | a0004 | c0008 | t0001 | g0293 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01433 | hp1 | a0004 | c0008 | t0001 | g0294 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01433 | hp2 | a0003 | c0003 | t0004 | g0227 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0074 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01515 | hp2 | a0007 | c0010 | t0002 | g0179 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0021 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0057 | EUR | IBS | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01884 | hp1 | a0004 | c0009 | t0008 | g0024 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01884 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01928 | hp2 | a0003 | c0003 | t0004 | g0220 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01934 | hp1 | a0004 | c0015 | t0003 | g0027 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01934 | hp2 | a0001 | c0005 | t0005 | g0167 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01952 | hp2 | a0003 | c0003 | t0004 | g0136 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0346 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01978 | hp1 | a0003 | c0003 | t0004 | g0225 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0344 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0351 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01981 | hp2 | a0003 | c0003 | t0004 | g0113 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01993 | hp2 | a0002 | c0001 | t0003 | g0210 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02004 | hp1 | a0003 | c0003 | t0004 | g0112 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0063 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02055 | hp1 | a0006 | c0006 | t0007 | g0080 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02055 | hp2 | a0002 | c0001 | t0003 | g0249 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0065 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0064 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02074 | hp2 | a0001 | c0013 | t0005 | g0273 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02080 | hp1 | a0001 | c0026 | t0002 | g0162 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02080 | hp2 | a0002 | c0001 | t0003 | g0252 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02083 | hp2 | a0003 | c0003 | t0004 | g0134 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0318 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02132 | hp2 | a0002 | c0001 | t0004 | g0193 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02135 | hp2 | a0003 | c0003 | t0017 | g0229 | EAS | KHV | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02145 | hp2 | a0004 | c0034 | t0007 | g0042 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02155 | hp1 | a0004 | c0004 | t0001 | g0309 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02155 | hp2 | a0001 | c0005 | t0005 | g0172 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0075 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02257 | hp1 | a0003 | c0003 | t0004 | g0116 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02257 | hp2 | a0004 | c0004 | t0001 | g0289 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02258 | hp1 | a0013 | c0019 | t0004 | g0054 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02258 | hp2 | a0002 | c0001 | t0003 | g0189 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02273 | hp1 | a0003 | c0003 | t0004 | g0007 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0342 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02280 | hp1 | a0004 | c0004 | t0001 | g0312 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02280 | hp2 | a0001 | c0002 | t0022 | g0337 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02293 | hp1 | a0003 | c0003 | t0004 | g0007 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0332 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02300 | hp2 | a0003 | c0003 | t0004 | g0123 | AMR | PEL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02451 | hp1 | a0014 | c0030 | t0021 | g0041 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02451 | hp2 | a0006 | c0006 | t0007 | g0052 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02572 | hp1 | a0003 | c0003 | t0005 | g0303 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02572 | hp2 | a0015 | c0029 | t0012 | g0082 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0343 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02602 | hp2 | a0016 | c0025 | t0001 | g0284 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02615 | hp1 | a0004 | c0004 | t0015 | g0019 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02630 | hp1 | a0010 | c0014 | t0013 | g0181 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02647 | hp1 | a0004 | c0004 | t0001 | g0019 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02647 | hp2 | a0003 | c0003 | t0005 | g0322 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02683 | hp1 | a0004 | c0009 | t0008 | g0025 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02683 | hp2 | a0003 | c0003 | t0004 | g0124 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02698 | hp1 | a0001 | c0005 | t0005 | g0166 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02698 | hp2 | a0003 | c0003 | t0004 | g0109 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02717 | hp1 | a0004 | c0031 | t0001 | g0287 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02717 | hp2 | a0003 | c0003 | t0005 | g0008 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02723 | hp1 | a0002 | c0001 | t0003 | g0100 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02723 | hp2 | a0003 | c0003 | t0004 | g0115 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02735 | hp1 | a0004 | c0008 | t0001 | g0297 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02735 | hp2 | a0017 | c0016 | t0004 | g0125 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0066 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02809 | hp1 | a0002 | c0001 | t0003 | g0138 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02809 | hp2 | a0002 | c0001 | t0001 | g0061 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02818 | hp1 | a0003 | c0003 | t0004 | g0221 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02818 | hp2 | a0010 | c0014 | t0013 | g0248 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02886 | hp1 | a0002 | c0001 | t0009 | g0182 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02895 | hp1 | a0018 | c0039 | t0009 | g0196 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0334 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02896 | hp2 | a0003 | c0003 | t0005 | g0120 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02897 | hp1 | a0003 | c0003 | t0005 | g0086 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02922 | hp1 | a0006 | c0006 | t0008 | g0048 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02922 | hp2 | a0002 | c0001 | t0003 | g0012 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0288 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0127 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02976 | hp2 | a0006 | c0006 | t0007 | g0078 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03017 | hp1 | a0002 | c0001 | t0003 | g0098 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03041 | hp1 | a0002 | c0001 | t0003 | g0230 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03041 | hp2 | a0019 | c0032 | t0020 | g0191 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03098 | hp1 | a0006 | c0006 | t0007 | g0051 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03098 | hp2 | a0020 | c0017 | t0004 | g0180 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03130 | hp1 | a0021 | c0033 | t0001 | g0280 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03130 | hp2 | a0008 | c0011 | t0012 | g0083 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03139 | hp1 | a0002 | c0001 | t0003 | g0012 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03139 | hp2 | a0002 | c0001 | t0009 | g0250 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0335 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03209 | hp2 | a0002 | c0001 | t0003 | g0195 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03225 | hp1 | a0004 | c0004 | t0001 | g0286 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03225 | hp2 | a0022 | c0035 | t0013 | g0049 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03239 | hp1 | a0004 | c0004 | t0001 | g0298 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03239 | hp2 | a0003 | c0003 | t0004 | g0107 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03453 | hp1 | a0001 | c0005 | t0005 | g0325 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03453 | hp2 | a0003 | c0003 | t0005 | g0119 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03486 | hp1 | a0002 | c0001 | t0003 | g0357 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03486 | hp2 | a0004 | c0004 | t0001 | g0290 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03490 | hp1 | a0002 | c0001 | t0003 | g0013 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0283 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03491 | hp1 | a0004 | c0008 | t0001 | g0301 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03491 | hp2 | a0002 | c0001 | t0003 | g0097 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03492 | hp1 | a0002 | c0001 | t0003 | g0013 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03492 | hp2 | a0004 | c0008 | t0001 | g0302 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03516 | hp1 | a0002 | c0001 | t0003 | g0137 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03516 | hp2 | a0002 | c0001 | t0003 | g0358 | AFR | ESN | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03540 | hp1 | a0002 | c0001 | t0001 | g0060 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03540 | hp2 | a0003 | c0003 | t0004 | g0101 | AFR | GWD | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0117 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03579 | hp2 | a0008 | c0011 | t0012 | g0084 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03654 | hp2 | a0003 | c0003 | t0004 | g0219 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03669 | hp2 | a0001 | c0005 | t0016 | g0267 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03688 | hp1 | a0001 | c0005 | t0005 | g0271 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03704 | hp1 | a0002 | c0001 | t0003 | g0099 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03704 | hp2 | a0011 | c0012 | t0006 | g0262 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03710 | hp1 | a0011 | c0012 | t0006 | g0260 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03710 | hp2 | a0001 | c0005 | t0005 | g0036 | SAS | PJL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03831 | hp1 | a0003 | c0003 | t0004 | g0111 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03831 | hp2 | a0001 | c0005 | t0005 | g0235 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03834 | hp1 | a0003 | c0003 | t0011 | g0122 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03834 | hp2 | a0023 | c0023 | t0006 | g0034 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03927 | hp2 | a0001 | c0005 | t0005 | g0269 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0242 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04115 | hp2 | a0001 | c0005 | t0005 | g0266 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04184 | hp1 | a0001 | c0005 | t0005 | g0035 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04184 | hp2 | a0003 | c0003 | t0004 | g0110 | SAS | BEB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04199 | hp1 | a0005 | c0007 | t0006 | g0033 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04199 | hp2 | a0004 | c0008 | t0001 | g0295 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04204 | hp1 | a0001 | c0005 | t0005 | g0275 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04228 | hp1 | a0003 | c0003 | t0004 | g0108 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG04228 | hp2 | a0004 | c0004 | t0018 | g0307 | SAS | STU | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18522 | hp2 | a0003 | c0003 | t0005 | g0121 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18612 | hp1 | a0002 | c0001 | t0003 | g0348 | EAS | CHB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18612 | hp2 | a0002 | c0001 | t0003 | g0203 | EAS | CHB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18906 | hp1 | a0001 | c0005 | t0025 | g0081 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18906 | hp2 | a0003 | c0003 | t0004 | g0132 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18940 | hp1 | a0001 | c0002 | t0005 | g0153 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18940 | hp2 | a0002 | c0001 | t0003 | g0258 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18944 | hp2 | a0024 | c0028 | t0004 | g0163 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18945 | hp1 | a0002 | c0001 | t0003 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18945 | hp2 | a0004 | c0004 | t0001 | g0096 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18946 | hp1 | a0001 | c0005 | t0005 | g0168 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18946 | hp2 | a0002 | c0001 | t0003 | g0201 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0274 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18950 | hp1 | a0001 | c0005 | t0005 | g0169 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18950 | hp2 | a0002 | c0001 | t0003 | g0215 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18954 | hp1 | a0002 | c0001 | t0003 | g0069 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18954 | hp2 | a0001 | c0002 | t0005 | g0158 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18956 | hp1 | a0005 | c0007 | t0006 | g0264 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0277 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18957 | hp2 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18959 | hp1 | a0004 | c0004 | t0001 | g0050 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18960 | hp1 | a0003 | c0003 | t0004 | g0130 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18960 | hp2 | a0001 | c0005 | t0005 | g0146 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18964 | hp1 | a0003 | c0003 | t0004 | g0106 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18966 | hp2 | a0002 | c0001 | t0003 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18967 | hp1 | a0002 | c0001 | t0003 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18967 | hp2 | a0002 | c0001 | t0003 | g0177 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18968 | hp1 | a0004 | c0004 | t0001 | g0306 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18970 | hp1 | a0001 | c0005 | t0005 | g0015 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18971 | hp2 | a0002 | c0001 | t0003 | g0254 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18972 | hp1 | a0004 | c0004 | t0001 | g0305 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18972 | hp2 | a0003 | c0003 | t0004 | g0037 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18973 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0197 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18974 | hp1 | a0002 | c0001 | t0003 | g0183 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18974 | hp2 | a0002 | c0001 | t0003 | g0176 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18977 | hp2 | a0001 | c0036 | t0005 | g0170 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18978 | hp1 | a0001 | c0005 | t0005 | g0244 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18978 | hp2 | a0005 | c0007 | t0006 | g0265 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18979 | hp2 | a0003 | c0003 | t0011 | g0228 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18980 | hp2 | a0003 | c0003 | t0002 | g0131 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18982 | hp2 | a0004 | c0004 | t0001 | g0006 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18983 | hp1 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18986 | hp2 | a0002 | c0001 | t0003 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18988 | hp1 | a0003 | c0003 | t0004 | g0135 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18988 | hp2 | a0002 | c0001 | t0003 | g0207 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18989 | hp1 | a0002 | c0001 | t0003 | g0256 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18989 | hp2 | a0004 | c0004 | t0010 | g0076 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18990 | hp1 | a0002 | c0001 | t0003 | g0209 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18990 | hp2 | a0001 | c0005 | t0005 | g0087 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18991 | hp1 | a0003 | c0003 | t0004 | g0102 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18991 | hp2 | a0002 | c0001 | t0003 | g0255 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18992 | hp1 | a0002 | c0001 | t0003 | g0208 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0355 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18995 | hp2 | a0002 | c0001 | t0002 | g0164 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18998 | hp1 | a0001 | c0005 | t0005 | g0015 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18999 | hp1 | a0002 | c0001 | t0003 | g0213 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19000 | hp2 | a0002 | c0001 | t0003 | g0257 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19001 | hp1 | a0004 | c0004 | t0001 | g0006 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19001 | hp2 | a0001 | c0005 | t0005 | g0173 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19002 | hp1 | a0003 | c0003 | t0004 | g0141 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19002 | hp2 | a0004 | c0004 | t0010 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0278 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19003 | hp2 | a0003 | c0003 | t0004 | g0143 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19004 | hp1 | a0002 | c0001 | t0003 | g0200 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19004 | hp2 | a0004 | c0004 | t0010 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19010 | hp1 | a0004 | c0004 | t0001 | g0070 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19011 | hp1 | a0025 | c0024 | t0005 | g0144 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19012 | hp1 | a0002 | c0001 | t0003 | g0001 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19030 | hp1 | a0004 | c0004 | t0001 | g0304 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19030 | hp2 | a0026 | c0018 | t0014 | g0263 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19043 | hp1 | a0002 | c0001 | t0024 | g0092 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19043 | hp2 | a0003 | c0003 | t0004 | g0103 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19054 | hp1 | a0003 | c0003 | t0004 | g0038 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19054 | hp2 | a0005 | c0007 | t0006 | g0261 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19056 | hp2 | a0001 | c0005 | t0005 | g0091 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19057 | hp1 | a0004 | c0004 | t0001 | g0068 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19057 | hp2 | a0002 | c0001 | t0003 | g0205 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19058 | hp1 | a0003 | c0003 | t0004 | g0104 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19058 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19060 | hp1 | a0003 | c0003 | t0004 | g0139 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19060 | hp2 | a0001 | c0002 | t0005 | g0240 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19062 | hp1 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19062 | hp2 | a0003 | c0003 | t0004 | g0114 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19067 | hp1 | a0002 | c0001 | t0003 | g0184 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19067 | hp2 | a0002 | c0001 | t0003 | g0095 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19074 | hp1 | a0004 | c0004 | t0001 | g0067 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19075 | hp1 | a0004 | c0004 | t0001 | g0327 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19075 | hp2 | a0001 | c0002 | t0004 | g0165 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19077 | hp1 | a0005 | c0007 | t0006 | g0032 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19077 | hp2 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19078 | hp1 | a0002 | c0001 | t0003 | g0202 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19078 | hp2 | a0001 | c0005 | t0005 | g0245 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19079 | hp1 | a0002 | c0001 | t0003 | g0204 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19080 | hp1 | a0003 | c0003 | t0004 | g0105 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19080 | hp2 | a0002 | c0001 | t0003 | g0174 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19081 | hp2 | a0002 | c0001 | t0003 | g0212 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19085 | hp1 | a0003 | c0003 | t0004 | g0140 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19085 | hp2 | a0002 | c0001 | t0003 | g0319 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19087 | hp1 | a0004 | c0004 | t0001 | g0030 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19087 | hp2 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19088 | hp1 | a0002 | c0001 | t0003 | g0198 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19090 | hp1 | a0002 | c0001 | t0003 | g0206 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19090 | hp2 | a0004 | c0004 | t0001 | g0310 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19240 | hp1 | a0003 | c0003 | t0004 | g0222 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA19240 | hp2 | a0002 | c0001 | t0003 | g0350 | AFR | YRI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20129 | hp1 | a0008 | c0011 | t0007 | g0031 | AFR | ASW | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0062 | AFR | ASW | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20752 | hp1 | a0004 | c0009 | t0008 | g0029 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0005 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20805 | hp1 | a0004 | c0009 | t0008 | g0026 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20805 | hp2 | a0001 | c0005 | t0005 | g0268 | EUR | TSI | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01123 | hp1 | a0012 | c0037 | t0005 | g0324 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02109 | hp2 | a0006 | c0006 | t0007 | g0079 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02486 | hp1 | a0003 | c0003 | t0004 | g0128 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02486 | hp2 | a0001 | c0027 | t0002 | g0336 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02559 | hp1 | a0009 | c0020 | t0014 | g0321 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG02559 | hp2 | a0004 | c0004 | t0001 | g0279 | AFR | ACB | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0118 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0285 | AFR | MSL | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG06807 | hp1 | a0002 | c0001 | t0003 | g0188 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
HG06807 | hp2 | a0009 | c0021 | t0019 | g0085 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0276 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA18955 | hp2 | a0001 | c0013 | t0005 | g0232 | EAS | JPT | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0338 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA20300 | hp2 | a0003 | c0022 | t0005 | g0223 | AFR | USA | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA21309 | hp1 | a0002 | c0001 | t0001 | g0005 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
NA21309 | hp2 | a0002 | c0001 | t0003 | g0359 | AFR | LWK | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
homoSapiens | chm13v2 | a0001 | c0005 | t0005 | g0272 | REF | REF | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
homoSapiens | grch38p0 | a0001 | c0005 | t0005 | g0071 | REF | REF | CEP164_chr11_117322854_117418266 | CEP164 | chr11 | 117322854 | 117418266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117351876 | G | A | 10 | a0003 a0005 a0006 others(7): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
missense_variant | MODERATE | c.281G>A | p.Ser94Asn | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/33 | 429/5629 | 281/4383 | 94/1460 | chr11 | 117351876 | |||
chr11:117361893 | G | A | 1 | a0025 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.452G>A | p.Arg151Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 600/5629 | 452/4383 | 151/1460 | chr11 | 117361893 | |||
chr11:117361898 | C | T | 1 | a0018 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.457C>T | p.Leu153Phe | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 605/5629 | 457/4383 | 153/1460 | chr11 | 117361898 | |||
chr11:117361989 | T | A | 1 | a0016 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.548T>A | p.Met183Lys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/33 | 696/5629 | 548/4383 | 183/1460 | chr11 | 117361989 | |||
chr11:117381721 | A | G | 1 | a0007 | 4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
missense_variant | MODERATE | c.1430A>G | p.His477Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1578/5629 | 1430/4383 | 477/1460 | chr11 | 117381721 | |||
chr11:117381775 | C | G | 3 | a0005 a0011 a0023 |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
missense_variant | MODERATE | c.1484C>G | p.Pro495Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1632/5629 | 1484/4383 | 495/1460 | chr11 | 117381775 | |||
chr11:117382909 | C | T | 1 | a0022 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1691C>T | p.Ala564Val | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/33 | 1839/5629 | 1691/4383 | 564/1460 | chr11 | 117382909 | |||
chr11:117393037 | G | A | 1 | a0017 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2527G>A | p.Val843Met | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/33 | 2675/5629 | 2527/4383 | 843/1460 | chr11 | 117393037 | |||
chr11:117395136 | G | A | 1 | a0024 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.2858G>A | p.Arg953Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/33 | 3006/5629 | 2858/4383 | 953/1460 | chr11 | 117395136 | |||
chr11:117395596 | C | G | 2 | a0002 a0018 |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
missense_variant | MODERATE | c.2963C>G | p.Thr988Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3111/5629 | 2963/4383 | 988/1460 | chr11 | 117395596 | |||
chr11:117395652 | C | T | 1 | a0021 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3019C>T | p.Arg1007Cys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3167/5629 | 3019/4383 | 1007/1460 | chr11 | 117395652 | |||
chr11:117395665 | T | C | 1 | a0020 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3032T>C | p.Leu1011Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/33 | 3180/5629 | 3032/4383 | 1011/1460 | chr11 | 117395665 | |||
chr11:117397144 | G | A | 1 | a0026 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.3332G>A | p.Arg1111His | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3480/5629 | 3332/4383 | 1111/1460 | chr11 | 117397144 | |||
chr11:117397168 | A | G | 15 | a0002 a0004 a0005 others(12): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
missense_variant | MODERATE | c.3356A>G | p.Gln1119Arg | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3504/5629 | 3356/4383 | 1119/1460 | chr11 | 117397168 | |||
chr11:117397176 | C | T | 1 | a0011 | 2 | HG03704.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.3364C>T | p.Arg1122Cys | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3512/5629 | 3364/4383 | 1122/1460 | chr11 | 117397176 | |||
chr11:117397177 | G | A | 1 | a0013 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3365G>A | p.Arg1122His | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/33 | 3513/5629 | 3365/4383 | 1122/1460 | chr11 | 117397177 | |||
chr11:117408996 | C | T | 7 | a0005 a0009 a0010 others(4): Show |
15 | HG00597.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
missense_variant | MODERATE | c.3716C>T | p.Pro1239Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 29/33 | 3864/5629 | 3716/4383 | 1239/1460 | chr11 | 117408996 | |||
chr11:117409642 | C | T | 1 | a0014 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.3773C>T | p.Ser1258Phe | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 3921/5629 | 3773/4383 | 1258/1460 | chr11 | 117409642 | |||
chr11:117409773 | C | T | 1 | a0012 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.3904C>T | p.Pro1302Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4052/5629 | 3904/4383 | 1302/1460 | chr11 | 117409773 | |||
chr11:117409801 | C | G | 5 | a0008 a0009 a0015 others(2): Show |
8 | HG02559.hp1 HG02572.hp2 HG03041.hp2 others(5): Show |
missense_variant | MODERATE | c.3932C>G | p.Thr1311Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4080/5629 | 3932/4383 | 1311/1460 | chr11 | 117409801 | |||
chr11:117409894 | C | T | 1 | a0015 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.4025C>T | p.Pro1342Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4173/5629 | 4025/4383 | 1342/1460 | chr11 | 117409894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117371142 | C | T | 1 | a0002c0038 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.828C>T | p.Ala276Ala | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/33 | 976/5629 | 828/4383 | 276/1460 | chr11 | 117371142 | |||
chr11:117380676 | G | A | 1 | a0001c0026 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1380G>A | p.Gln460Gln | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/33 | 1528/5629 | 1380/4383 | 460/1460 | chr11 | 117380676 | |||
chr11:117381773 | T | C | 34 | a0001c0002 a0001c0013 a0001c0026 others(31): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
synonymous_variant | LOW | c.1482T>C | p.Pro494Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/33 | 1630/5629 | 1482/4383 | 494/1460 | chr11 | 117381773 | |||
chr11:117382925 | G | T | 1 | a0003c0022 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1707G>T | p.Pro569Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/33 | 1855/5629 | 1707/4383 | 569/1460 | chr11 | 117382925 | |||
chr11:117391137 | C | T | 2 | a0004c0009 a0004c0015 |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
synonymous_variant | LOW | c.2205C>T | p.Ser735Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/33 | 2353/5629 | 2205/4383 | 735/1460 | chr11 | 117391137 | |||
chr11:117392243 | G | A | 1 | a0001c0027 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2301G>A | p.Glu767Glu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 18/33 | 2449/5629 | 2301/4383 | 767/1460 | chr11 | 117392243 | |||
chr11:117394388 | C | T | 1 | a0004c0034 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.2655C>T | p.Thr885Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 21/33 | 2803/5629 | 2655/4383 | 885/1460 | chr11 | 117394388 | |||
chr11:117396558 | C | T | 2 | a0009c0021 a0019c0032 |
2 | HG03041.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3225C>T | p.Thr1075Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/33 | 3373/5629 | 3225/4383 | 1075/1460 | chr11 | 117396558 | |||
chr11:117407979 | C | T | 1 | a0004c0031 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3556C>T | p.Leu1186Leu | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/33 | 3704/5629 | 3556/4383 | 1186/1460 | chr11 | 117407979 | |||
chr11:117409796 | C | T | 7 | a0008c0011 a0009c0020 a0009c0021 others(4): Show |
9 | HG02559.hp1 HG02572.hp2 HG03041.hp2 others(6): Show |
synonymous_variant | LOW | c.3927C>T | p.Thr1309Thr | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/33 | 4075/5629 | 3927/4383 | 1309/1460 | chr11 | 117409796 | |||
chr11:117410850 | C | T | 1 | a0004c0008 | 6 | HG01361.hp2 HG01433.hp1 HG02735.hp1 others(3): Show |
synonymous_variant | LOW | c.4119C>T | p.Asn1373Asn | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4267/5629 | 4119/4383 | 1373/1460 | chr11 | 117410850 | |||
chr11:117410862 | G | A | 1 | a0009c0021 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4131G>A | p.Pro1377Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4279/5629 | 4131/4383 | 1377/1460 | chr11 | 117410862 | |||
chr11:117410862 | G | T | 1 | a0001c0036 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.4131G>T | p.Pro1377Pro | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/33 | 4279/5629 | 4131/4383 | 1377/1460 | chr11 | 117410862 | |||
chr11:117412084 | G | T | 34 | a0001c0002 a0001c0026 a0001c0027 others(31): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
synonymous_variant | LOW | c.4299G>T | p.Ser1433Ser | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 4447/5629 | 4299/4383 | 1433/1460 | chr11 | 117412084 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117327893 | C | T | 3 | a0001c0005t0025 a0002c0001t0009 a0018c0039t0009 |
6 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/33 | chr11 | 117327893 | |||||||
chr11:117412185 | T | C | 1 | a0004c0004t0010 | 3 | NA18989.hp2 NA19002.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 17 | chr11 | 117412185 | ||||||
chr11:117412226 | G | A | 1 | a0004c0004t0015 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 58 | chr11 | 117412226 | ||||||
chr11:117412263 | C | G | 9 | a0001c0002t0003 a0002c0001t0003 a0002c0001t0009 others(6): Show |
84 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*95C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 95 | chr11 | 117412263 | ||||||
chr11:117412306 | G | T | 1 | a0001c0002t0023 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 138 | chr11 | 117412306 | ||||||
chr11:117412339 | A | G | 1 | a0001c0002t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 171 | chr11 | 117412339 | ||||||
chr11:117412375 | C | T | 31 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0022 others(28): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 207 | chr11 | 117412375 | ||||||
chr11:117412425 | C | T | 2 | a0008c0011t0012 a0015c0029t0012 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*257C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 257 | chr11 | 117412425 | ||||||
chr11:117412755 | C | T | 20 | a0001c0002t0003 a0002c0001t0003 a0002c0001t0009 others(17): Show |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*587C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 587 | chr11 | 117412755 | ||||||
chr11:117412771 | A | G | 1 | a0002c0001t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 603 | chr11 | 117412771 | ||||||
chr11:117412888 | G | A | 2 | a0009c0021t0019 a0019c0032t0020 |
2 | HG03041.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*720G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 720 | chr11 | 117412888 | ||||||
chr11:117412910 | A | G | 13 | a0001c0002t0003 a0002c0001t0003 a0002c0001t0009 others(10): Show |
92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*742A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 742 | chr11 | 117412910 | ||||||
chr11:117412918 | A | G | 13 | a0001c0002t0003 a0002c0001t0003 a0002c0001t0009 others(10): Show |
92 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 750 | chr11 | 117412918 | ||||||
chr11:117412927 | A | G | 1 | a0014c0030t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*759A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 759 | chr11 | 117412927 | ||||||
chr11:117412948 | T | C | 2 | a0010c0014t0013 a0022c0035t0013 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 780 | chr11 | 117412948 | ||||||
chr11:117412960 | T | C | 36 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0023 others(33): Show |
199 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*792T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 792 | chr11 | 117412960 | ||||||
chr11:117413092 | C | T | 9 | a0001c0002t0004 a0002c0001t0004 a0003c0003t0004 others(6): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*924C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 924 | chr11 | 117413092 | ||||||
chr11:117413105 | A | G | 3 | a0005c0007t0006 a0011c0012t0006 a0023c0023t0006 |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*937A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 937 | chr11 | 117413105 | ||||||
chr11:117413160 | C | T | 1 | a0004c0004t0018 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 992 | chr11 | 117413160 | ||||||
chr11:117413223 | G | A | 5 | a0002c0001t0009 a0004c0009t0008 a0006c0006t0008 others(2): Show |
11 | HG01074.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1055G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1055 | chr11 | 117413223 | ||||||
chr11:117413251 | G | GT | 4 | a0003c0003t0011 a0009c0020t0014 a0019c0032t0020 others(1): Show |
6 | HG00140.hp1 HG02559.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1094dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1095 | INFO_REALIGN_3_PRIME | chr11 | 117413251 | |||||
chr11:117413252 | T | G | 1 | a0003c0003t0017 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1084T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 33/33 | 1084 | chr11 | 117413252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117327922 | T | C | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98+18T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117327922 | |||||||
chr11:117327982 | T | G | 1 | a0004c0004t0001g0030 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-98+78T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117327982 | |||||||
chr11:117328073 | A | T | 89 | a0001c0002t0001g0300 a0001c0002t0001g0311 a0001c0002t0001g0320 others(86): Show |
94 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-98+169A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328073 | |||||||
chr11:117328203 | T | G | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-98+299T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328203 | |||||||
chr11:117328258 | C | T | 3 | a0002c0001t0003g0357 a0002c0001t0003g0358 a0002c0001t0003g0359 |
3 | HG03486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-98+354C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328258 | |||||||
chr11:117328448 | T | C | 5 | a0001c0005t0005g0035 a0001c0005t0005g0036 a0005c0007t0006g0032 others(2): Show |
5 | HG03710.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98+544T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328448 | |||||||
chr11:117328455 | C | T | 5 | a0002c0001t0001g0016 a0002c0001t0001g0017 a0002c0001t0001g0276 others(2): Show |
7 | NA18955.hp1 NA18957.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-98+551C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328455 | |||||||
chr11:117328601 | C | T | 22 | a0001c0005t0005g0035 a0001c0005t0005g0036 a0001c0005t0005g0266 others(19): Show |
22 | HG00597.hp2 HG01168.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.-98+697C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328601 | |||||||
chr11:117328769 | A | G | 1 | a0001c0005t0005g0036 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-98+865A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328769 | |||||||
chr11:117328912 | G | C | 2 | a0003c0003t0004g0037 a0003c0003t0004g0038 |
2 | NA18972.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-98+1008G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117328912 | |||||||
chr11:117329026 | T | G | 30 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(27): Show |
30 | HG00597.hp2 HG01168.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-98+1122T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329026 | |||||||
chr11:117329154 | C | T | 125 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(122): Show |
130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-98+1250C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329154 | |||||||
chr11:117329413 | C | T | 1 | a0001c0002t0002g0356 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-98+1509C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329413 | |||||||
chr11:117329580 | C | T | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-98+1676C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329580 | |||||||
chr11:117329726 | G | C | 1 | a0001c0002t0002g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-98+1822G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329726 | |||||||
chr11:117329839 | C | CT | 65 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(62): Show |
69 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-98+1958dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | ||||||
chr11:117329839 | C | CTT | 141 | a0001c0002t0001g0046 a0001c0002t0002g0002 a0001c0002t0002g0010 others(138): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-98+1957_-98+1958d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | ||||||
chr11:117329839 | C | CTTT | 41 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0002g0231 others(38): Show |
42 | HG00408.hp2 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-98+1956_-98+1958d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | ||||||
chr11:117329839 | CT | C | 28 | a0001c0002t0001g0300 a0004c0004t0001g0018 a0004c0004t0001g0050 others(25): Show |
29 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-98+1958delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329839 | ||||||
chr11:117329862 | T | A | 1 | a0001c0005t0005g0036 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-98+1958T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329862 | |||||||
chr11:117329862 | T | TA | 8 | a0001c0005t0005g0035 a0005c0007t0006g0032 a0005c0007t0006g0033 others(5): Show |
8 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+1960dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117329862 | ||||||
chr11:117329922 | T | A | 41 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(38): Show |
41 | HG00323.hp1 HG00597.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.-98+2018T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117329922 | |||||||
chr11:117330037 | T | G | 41 | a0001c0002t0001g0300 a0001c0002t0001g0311 a0001c0002t0001g0328 others(38): Show |
42 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-98+2133T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330037 | |||||||
chr11:117330046 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-98+2142T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330046 | |||||||
chr11:117330227 | T | G | 261 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(258): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-98+2323T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330227 | |||||||
chr11:117330258 | C | T | 3 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 |
3 | HG01167.hp2 HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-98+2354C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330258 | |||||||
chr11:117330340 | T | A | 8 | a0001c0002t0001g0040 a0001c0002t0001g0053 a0001c0002t0001g0246 others(5): Show |
8 | HG01167.hp2 HG01175.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+2436T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330340 | |||||||
chr11:117330362 | G | A | 1 | a0022c0035t0013g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-98+2458G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330362 | |||||||
chr11:117330381 | G | T | 157 | a0001c0002t0001g0300 a0001c0002t0001g0311 a0001c0002t0001g0320 others(154): Show |
171 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.-98+2477G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330381 | |||||||
chr11:117330449 | T | G | 90 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-98+2545T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330449 | |||||||
chr11:117330450 | C | G | 1 | a0004c0004t0001g0312 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98+2546C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330450 | |||||||
chr11:117330506 | G | A | 1 | a0025c0024t0005g0144 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-98+2602G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330506 | |||||||
chr11:117330584 | G | A | 1 | a0002c0001t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-98+2680G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330584 | |||||||
chr11:117330643 | C | CT | 3 | a0002c0001t0003g0216 a0002c0001t0003g0217 a0002c0001t0003g0218 |
3 | HG00438.hp1 HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-98+2740dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117330643 | ||||||
chr11:117330649 | CA | C | 66 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-98+2754delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117330649 | ||||||
chr11:117330688 | A | G | 2 | a0004c0008t0001g0301 a0004c0008t0001g0302 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-98+2784A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330688 | |||||||
chr11:117330742 | A | G | 32 | a0002c0001t0003g0014 a0002c0001t0003g0097 a0002c0001t0003g0098 others(29): Show |
33 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.-98+2838A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330742 | |||||||
chr11:117330746 | A | T | 1 | a0004c0004t0010g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-98+2842A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330746 | |||||||
chr11:117330788 | T | C | 1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-98+2884T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330788 | |||||||
chr11:117330954 | A | G | 3 | a0001c0002t0001g0040 a0001c0002t0001g0311 a0001c0002t0001g0328 |
3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-98+3050A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330954 | |||||||
chr11:117330966 | T | C | 263 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(260): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-98+3062T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117330966 | |||||||
chr11:117331033 | C | G | 74 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-98+3129C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331033 | |||||||
chr11:117331047 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-98+3143G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331047 | |||||||
chr11:117331255 | A | G | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-98+3351A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331255 | |||||||
chr11:117331281 | C | T | 169 | a0001c0002t0001g0040 a0001c0002t0001g0053 a0001c0002t0001g0246 others(166): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-98+3377C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331281 | |||||||
chr11:117331430 | C | CA | 263 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(260): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-98+3526_-98+3527i others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331430 | |||||||
chr11:117331643 | C | T | 1 | a0002c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-98+3739C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331643 | |||||||
chr11:117331721 | G | A | 169 | a0001c0002t0001g0040 a0001c0002t0001g0053 a0001c0002t0001g0246 others(166): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-98+3817G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331721 | |||||||
chr11:117331750 | A | AT | 71 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(68): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-97-3841dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331750 | ||||||
chr11:117331750 | AT | A | 7 | a0002c0001t0001g0005 a0002c0001t0001g0057 a0002c0001t0001g0060 others(4): Show |
8 | HG01168.hp1 HG01175.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-97-3841delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331750 | ||||||
chr11:117331827 | G | A | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97-3778G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331827 | |||||||
chr11:117331918 | CA | C | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-97-3686delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117331918 | |||||||
chr11:117331981 | A | AAT | 223 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(220): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-97-3603_-97-3602d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | A | AATAT | 22 | a0001c0002t0001g0300 a0001c0002t0002g0047 a0001c0002t0002g0231 others(19): Show |
22 | HG00639.hp2 HG01109.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-97-3605_-97-3602d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | A | AATATAT | 42 | a0002c0001t0003g0001 a0002c0001t0003g0013 a0002c0001t0003g0099 others(39): Show |
48 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-97-3607_-97-3602d others(8): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | A | AATATATA others(1): Show |
12 | a0002c0001t0003g0012 a0002c0001t0003g0014 a0002c0001t0003g0097 others(9): Show |
14 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-97-3609_-97-3602d others(10): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | A | AATATATA others(3): Show |
4 | a0002c0001t0003g0100 a0002c0001t0003g0357 a0002c0001t0003g0358 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-97-3611_-97-3602d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | A | AATATATA others(5): Show |
1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-97-3613_-97-3602d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117331981 | AAT | A | 12 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(9): Show |
12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-97-3603_-97-3602d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117331981 | ||||||
chr11:117332004 | T | A | 1 | a0002c0001t0003g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-97-3601T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332004 | |||||||
chr11:117332064 | A | G | 12 | a0003c0003t0004g0037 a0003c0003t0004g0038 a0003c0003t0004g0135 others(9): Show |
12 | HG00408.hp1 HG01433.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.-97-3541A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332064 | |||||||
chr11:117332066 | C | T | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-97-3539C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332066 | |||||||
chr11:117332128 | C | T | 1 | a0003c0003t0004g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-97-3477C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332128 | |||||||
chr11:117332332 | T | G | 1 | a0002c0001t0003g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-97-3273T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332332 | |||||||
chr11:117332917 | A | G | 91 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(88): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-97-2688A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117332917 | |||||||
chr11:117333000 | A | C | 1 | a0003c0003t0004g0133 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-97-2605A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333000 | |||||||
chr11:117333202 | C | CAG | 285 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(282): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-97-2403_-97-2402i others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333202 | |||||||
chr11:117333216 | T | C | 1 | a0005c0007t0006g0033 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-97-2389T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333216 | |||||||
chr11:117333480 | T | C | 1 | a0002c0001t0001g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-97-2125T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333480 | |||||||
chr11:117333742 | C | T | 3 | a0002c0001t0003g0215 a0002c0001t0003g0257 a0002c0001t0003g0258 |
3 | NA18940.hp2 NA18950.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-97-1863C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333742 | |||||||
chr11:117333941 | G | A | 5 | a0003c0003t0004g0107 a0003c0003t0004g0108 a0003c0003t0004g0109 others(2): Show |
5 | HG02698.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1664G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333941 | |||||||
chr11:117333972 | G | A | 4 | a0003c0003t0004g0007 a0003c0003t0004g0112 a0003c0003t0004g0113 others(1): Show |
5 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1633G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117333972 | |||||||
chr11:117334078 | T | C | 1 | a0003c0003t0004g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-97-1527T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334078 | |||||||
chr11:117334228 | T | G | 1 | a0003c0003t0004g0135 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-97-1377T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334228 | |||||||
chr11:117334343 | T | C | 1 | a0002c0001t0003g0195 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-97-1262T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334343 | |||||||
chr11:117334784 | C | CA | 32 | a0001c0002t0001g0247 a0001c0002t0002g0346 a0001c0002t0002g0347 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-97-802dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | ||||||
chr11:117334784 | C | CAA | 170 | a0001c0002t0001g0040 a0001c0002t0001g0246 a0001c0002t0001g0300 others(167): Show |
188 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.-97-803_-97-802dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | ||||||
chr11:117334784 | C | CAAA | 7 | a0001c0002t0001g0053 a0001c0002t0002g0147 a0001c0002t0002g0233 others(4): Show |
7 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-97-804_-97-802dup others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | ||||||
chr11:117334784 | CA | C | 8 | a0001c0002t0001g0045 a0001c0002t0001g0074 a0002c0001t0001g0093 others(5): Show |
8 | HG01069.hp1 HG01168.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.-97-802delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117334784 | ||||||
chr11:117334827 | A | G | 1 | a0004c0004t0001g0070 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-97-778A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117334827 | |||||||
chr11:117335050 | T | C | 90 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-97-555T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335050 | |||||||
chr11:117335128 | G | T | 90 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-97-477G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335128 | |||||||
chr11:117335145 | C | T | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-97-460C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335145 | |||||||
chr11:117335149 | T | G | 1 | a0003c0003t0004g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-97-456T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335149 | |||||||
chr11:117335160 | G | C | 4 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97-445G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | chr11 | 117335160 | |||||||
chr11:117335579 | C | CT | 21 | a0001c0005t0005g0244 a0002c0001t0001g0093 a0002c0001t0003g0001 others(18): Show |
26 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.-97-8dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr11 | 117335579 | ||||||
chr11:117335712 | C | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-22+32C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117335712 | |||||||
chr11:117335971 | C | CT | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+292dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117335971 | ||||||
chr11:117335988 | C | T | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-22+308C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117335988 | |||||||
chr11:117336091 | G | T | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22+411G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336091 | |||||||
chr11:117336151 | A | G | 1 | a0001c0002t0001g0320 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-22+471A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336151 | |||||||
chr11:117336212 | CG | C | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-22+533delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336212 | |||||||
chr11:117336406 | G | C | 21 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(18): Show |
21 | HG00323.hp1 HG00597.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+726G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336406 | |||||||
chr11:117336798 | C | G | 1 | a0004c0004t0001g0309 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-22+1118C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336798 | |||||||
chr11:117336910 | T | C | 90 | a0001c0002t0002g0148 a0001c0002t0002g0231 a0001c0002t0002g0234 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-22+1230T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336910 | |||||||
chr11:117336912 | C | G | 90 | a0001c0002t0002g0148 a0001c0002t0002g0231 a0001c0002t0002g0234 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-22+1232C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336912 | |||||||
chr11:117336949 | G | T | 75 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0003g0175 others(72): Show |
83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-22+1269G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336949 | |||||||
chr11:117336980 | G | A | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1300G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336980 | |||||||
chr11:117336998 | A | T | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22+1318A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117336998 | |||||||
chr11:117337226 | T | A | 1 | a0002c0001t0003g0200 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-21-1340T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337226 | |||||||
chr11:117337510 | T | TAAAAAAA others(3): Show |
3 | a0003c0003t0004g0135 a0003c0003t0005g0086 a0005c0007t0006g0032 |
3 | HG02897.hp1 NA18988.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-21-1051_-21-1042d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(4): Show |
63 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(60): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-21-1052_-21-1042d others(13): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(5): Show |
4 | a0003c0003t0004g0102 a0006c0006t0007g0052 a0006c0006t0007g0078 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-1053_-21-1042d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(6): Show |
1 | a0006c0006t0007g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-21-1054_-21-1042d others(15): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(7): Show |
1 | a0006c0006t0007g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21-1055_-21-1042d others(16): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(21): Show |
1 | a0023c0023t0006g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(30): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(22): Show |
3 | a0005c0007t0006g0033 a0005c0007t0006g0261 a0011c0012t0006g0262 |
3 | HG03704.hp2 HG04199.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(31): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(23): Show |
3 | a0005c0007t0006g0259 a0005c0007t0006g0264 a0011c0012t0006g0260 |
3 | HG00597.hp2 HG03710.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(32): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(24): Show |
1 | a0004c0009t0008g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(33): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(27): Show |
1 | a0005c0007t0006g0265 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(36): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(30): Show |
1 | a0004c0009t0008g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-21-1042_-21-1041i others(39): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337510 | T | TAAAAAAA others(31): Show |
2 | a0004c0009t0008g0024 a0004c0009t0008g0025 |
2 | HG01884.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-21-1042_-21-1041i others(40): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr11 | 117337510 | ||||||
chr11:117337554 | G | A | 85 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-1012G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337554 | |||||||
chr11:117337722 | G | A | 1 | a0004c0004t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-844G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337722 | |||||||
chr11:117337983 | C | T | 1 | a0001c0002t0002g0345 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-21-583C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117337983 | |||||||
chr11:117338003 | C | T | 1 | a0003c0003t0004g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-21-563C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338003 | |||||||
chr11:117338027 | C | T | 1 | a0001c0013t0005g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-21-539C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338027 | |||||||
chr11:117338031 | T | C | 85 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-535T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338031 | |||||||
chr11:117338122 | G | A | 1 | a0002c0001t0003g0174 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-21-444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338122 | |||||||
chr11:117338140 | C | T | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-21-426C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338140 | |||||||
chr11:117338233 | C | T | 74 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-21-333C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338233 | |||||||
chr11:117338297 | G | A | 1 | a0001c0005t0005g0087 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-21-269G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338297 | |||||||
chr11:117338441 | G | A | 1 | a0001c0002t0002g0333 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-21-125G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338441 | |||||||
chr11:117338449 | C | T | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-117C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338449 | |||||||
chr11:117338552 | C | T | 85 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-21-14C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 2/32 | chr11 | 117338552 | |||||||
chr11:117338697 | G | A | 1 | a0004c0004t0001g0283 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.82+29G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338697 | |||||||
chr11:117338879 | G | A | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+211G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338879 | |||||||
chr11:117338943 | G | A | 1 | a0003c0003t0004g0107 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.82+275G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117338943 | |||||||
chr11:117339070 | C | T | 2 | a0001c0002t0004g0355 a0002c0001t0002g0318 |
2 | HG02132.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.82+402C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339070 | |||||||
chr11:117339076 | C | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.82+408C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339076 | |||||||
chr11:117339132 | G | C | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.82+464G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339132 | |||||||
chr11:117339266 | G | T | 1 | a0001c0002t0002g0345 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.82+598G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339266 | |||||||
chr11:117339483 | T | C | 6 | a0002c0001t0003g0012 a0002c0001t0003g0100 a0002c0001t0003g0249 others(3): Show |
7 | HG02055.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+815T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339483 | |||||||
chr11:117339511 | CTTTGTTT | C | 17 | a0003c0003t0004g0038 a0003c0003t0004g0111 a0003c0003t0004g0113 others(14): Show |
17 | HG00408.hp1 HG00597.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.82+854_82+860delGT others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339511 | ||||||
chr11:117339515 | GTTTTTTG others(1): Show |
G | 65 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(62): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.82+854_82+861delGT others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339515 | ||||||
chr11:117339520 | TTG | T | 83 | a0001c0002t0001g0320 a0001c0002t0002g0010 a0001c0002t0002g0011 others(80): Show |
89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.82+854_82+855delGT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339520 | ||||||
chr11:117339521 | TG | T | 30 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0088 others(27): Show |
33 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.82+854delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339521 | |||||||
chr11:117339522 | G | T | 3 | a0001c0002t0002g0157 a0001c0005t0005g0325 a0007c0010t0002g0009 |
3 | HG01243.hp2 HG03453.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.82+854G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339522 | |||||||
chr11:117339522 | GT | G | 99 | a0001c0002t0003g0175 a0001c0005t0005g0004 a0002c0001t0001g0005 others(96): Show |
110 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+878delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339522 | ||||||
chr11:117339522 | GTT | G | 43 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(40): Show |
44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.82+877_82+878delTT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117339522 | ||||||
chr11:117339525 | T | G | 1 | a0001c0005t0005g0275 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82+857T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339525 | |||||||
chr11:117339530 | T | G | 1 | a0002c0001t0003g0014 | 2 | NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.82+862T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339530 | |||||||
chr11:117339531 | T | G | 3 | a0001c0002t0001g0300 a0004c0015t0003g0028 a0022c0035t0013g0049 |
3 | HG00323.hp1 HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.82+863T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339531 | |||||||
chr11:117339622 | G | A | 6 | a0004c0004t0001g0030 a0004c0004t0001g0305 a0004c0004t0001g0306 others(3): Show |
6 | HG02155.hp1 NA18968.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+954G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339622 | |||||||
chr11:117339631 | C | T | 11 | a0002c0001t0003g0069 a0002c0001t0003g0095 a0004c0004t0001g0003 others(8): Show |
13 | NA18945.hp2 NA18954.hp1 NA18959.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+963C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339631 | |||||||
chr11:117339991 | G | A | 85 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+1323G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117339991 | |||||||
chr11:117340005 | A | T | 1 | a0001c0002t0002g0333 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.82+1337A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340005 | |||||||
chr11:117340070 | G | A | 1 | a0001c0005t0005g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82+1402G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340070 | |||||||
chr11:117340172 | C | T | 6 | a0002c0001t0003g0012 a0002c0001t0003g0100 a0002c0001t0003g0249 others(3): Show |
7 | HG02055.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+1504C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340172 | |||||||
chr11:117340185 | T | C | 85 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+1517T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340185 | |||||||
chr11:117340268 | C | T | 5 | a0001c0002t0001g0320 a0001c0002t0002g0314 a0001c0002t0002g0315 others(2): Show |
5 | NA18941.hp1 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+1600C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340268 | |||||||
chr11:117340482 | G | A | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.82+1814G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340482 | |||||||
chr11:117340524 | G | T | 81 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.82+1856G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117340524 | |||||||
chr11:117340831 | TTC | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.82+2165_82+2166del others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117340831 | ||||||
chr11:117341078 | C | T | 1 | a0019c0032t0020g0191 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82+2410C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341078 | |||||||
chr11:117341207 | A | G | 1 | a0011c0012t0006g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82+2539A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341207 | |||||||
chr11:117341370 | A | G | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82+2702A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341370 | |||||||
chr11:117341415 | C | G | 2 | a0010c0014t0013g0181 a0010c0014t0013g0248 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.82+2747C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341415 | |||||||
chr11:117341437 | TTTG | T | 36 | a0001c0005t0005g0004 a0001c0005t0005g0015 a0001c0005t0005g0035 others(33): Show |
39 | HG00323.hp1 HG00423.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.83-2723_83-2721del others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117341437 | ||||||
chr11:117341455 | T | G | 1 | a0001c0005t0005g0244 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.83-2711T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341455 | |||||||
chr11:117341557 | C | T | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-2609C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341557 | |||||||
chr11:117341579 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83-2587G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341579 | |||||||
chr11:117341621 | G | T | 89 | a0002c0001t0001g0059 a0002c0001t0003g0216 a0002c0001t0003g0217 others(86): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.83-2545G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341621 | |||||||
chr11:117341924 | T | C | 86 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-2242T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117341924 | |||||||
chr11:117342176 | C | T | 86 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1990C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342176 | |||||||
chr11:117342192 | A | G | 67 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(64): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.83-1974A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342192 | |||||||
chr11:117342443 | C | T | 1 | a0007c0010t0002g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83-1723C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342443 | |||||||
chr11:117342444 | G | A | 86 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-1722G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342444 | |||||||
chr11:117342473 | G | A | 36 | a0004c0004t0001g0018 a0004c0004t0001g0019 a0004c0004t0001g0030 others(33): Show |
37 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.83-1693G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342473 | |||||||
chr11:117342754 | G | A | 4 | a0001c0002t0002g0150 a0001c0002t0002g0151 a0001c0002t0002g0152 others(1): Show |
4 | HG00609.hp1 NA18940.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-1412G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117342754 | |||||||
chr11:117343131 | A | G | 77 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(74): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.83-1035A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343131 | |||||||
chr11:117343177 | A | G | 43 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(40): Show |
44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.83-989A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343177 | |||||||
chr11:117343242 | G | T | 1 | a0003c0003t0011g0228 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.83-924G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343242 | |||||||
chr11:117343375 | G | A | 86 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-791G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343375 | |||||||
chr11:117343629 | C | CT | 84 | a0001c0002t0001g0328 a0001c0002t0002g0242 a0001c0002t0002g0243 others(81): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.83-519dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117343629 | ||||||
chr11:117343629 | C | CTT | 7 | a0003c0003t0002g0131 a0003c0003t0004g0110 a0003c0003t0004g0113 others(4): Show |
7 | HG00597.hp2 HG00741.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-520_83-519dupTT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr11 | 117343629 | ||||||
chr11:117343743 | G | C | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.83-423G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343743 | |||||||
chr11:117343864 | G | C | 257 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(254): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.83-302G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343864 | |||||||
chr11:117343966 | T | C | 2 | a0001c0002t0001g0311 a0001c0002t0001g0328 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.83-200T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117343966 | |||||||
chr11:117344032 | A | G | 2 | a0001c0002t0001g0053 a0001c0002t0001g0247 |
2 | HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.83-134A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 3/32 | chr11 | 117344032 | |||||||
chr11:117344290 | G | T | 3 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0026c0018t0014g0263 |
3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.194+13G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344290 | |||||||
chr11:117344297 | G | A | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+20G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344297 | |||||||
chr11:117344301 | A | G | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.194+24A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344301 | |||||||
chr11:117344352 | G | A | 5 | a0001c0002t0002g0020 a0001c0002t0002g0344 a0001c0002t0002g0346 others(2): Show |
6 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+75G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344352 | |||||||
chr11:117344389 | A | G | 1 | a0002c0001t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.194+112A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344389 | |||||||
chr11:117344656 | G | A | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+379G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344656 | |||||||
chr11:117344712 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.194+435A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344712 | |||||||
chr11:117344764 | T | C | 2 | a0002c0001t0003g0188 a0019c0032t0020g0191 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.194+487T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344764 | |||||||
chr11:117344889 | C | T | 34 | a0001c0005t0005g0004 a0001c0005t0005g0015 a0001c0005t0005g0035 others(31): Show |
37 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.194+612C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344889 | |||||||
chr11:117344974 | T | C | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194+697T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117344974 | |||||||
chr11:117345029 | G | A | 1 | a0002c0001t0003g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.194+752G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345029 | |||||||
chr11:117345297 | C | T | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.194+1020C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345297 | |||||||
chr11:117345497 | T | G | 88 | a0002c0001t0001g0059 a0003c0003t0002g0131 a0003c0003t0004g0007 others(85): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.194+1220T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345497 | |||||||
chr11:117345621 | G | A | 1 | a0004c0004t0001g0305 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.194+1344G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345621 | |||||||
chr11:117345635 | TG | T | 76 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(73): Show |
86 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.194+1359delG | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345635 | |||||||
chr11:117345712 | G | A | 1 | a0016c0025t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.194+1435G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345712 | |||||||
chr11:117345719 | T | C | 1 | a0002c0001t0003g0192 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.194+1442T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345719 | |||||||
chr11:117345784 | G | T | 1 | a0002c0001t0002g0318 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.194+1507G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345784 | |||||||
chr11:117345791 | G | C | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194+1514G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345791 | |||||||
chr11:117345883 | C | T | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.194+1606C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345883 | |||||||
chr11:117345887 | A | T | 55 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.194+1610A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345887 | |||||||
chr11:117345912 | C | T | 4 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+1635C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345912 | |||||||
chr11:117345967 | G | T | 5 | a0002c0001t0009g0182 a0002c0001t0009g0190 a0002c0001t0009g0250 others(2): Show |
5 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+1690G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117345967 | |||||||
chr11:117346001 | C | A | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+1724C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346001 | |||||||
chr11:117346266 | A | G | 1 | a0002c0001t0003g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.194+1989A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346266 | |||||||
chr11:117346391 | T | C | 1 | a0007c0010t0002g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.194+2114T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346391 | |||||||
chr11:117346455 | C | T | 1 | a0003c0003t0004g0135 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.194+2178C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346455 | |||||||
chr11:117346456 | G | A | 10 | a0002c0001t0003g0001 a0002c0001t0003g0183 a0002c0001t0003g0184 others(7): Show |
15 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+2179G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346456 | |||||||
chr11:117346558 | A | G | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+2281A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346558 | |||||||
chr11:117346675 | G | T | 160 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(157): Show |
174 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.194+2398G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346675 | |||||||
chr11:117346684 | C | T | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.194+2407C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346684 | |||||||
chr11:117346817 | C | G | 36 | a0001c0002t0001g0320 a0001c0002t0002g0020 a0001c0002t0002g0021 others(33): Show |
40 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.194+2540C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117346817 | |||||||
chr11:117347160 | TTTATTTG others(27): Show |
T | 1 | a0003c0003t0004g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.194+2884_194+2917d others(36): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347160 | |||||||
chr11:117347508 | C | T | 1 | a0003c0003t0004g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.194+3231C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347508 | |||||||
chr11:117347571 | G | A | 3 | a0002c0001t0001g0016 a0002c0001t0001g0276 a0002c0001t0001g0277 |
4 | NA18955.hp1 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+3294G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347571 | |||||||
chr11:117347590 | AT | A | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+3314delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347590 | |||||||
chr11:117347658 | C | T | 1 | a0001c0002t0002g0317 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.194+3381C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347658 | |||||||
chr11:117347710 | C | CA | 8 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(5): Show |
8 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.194+3447dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117347710 | ||||||
chr11:117347744 | T | C | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.194+3467T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117347744 | |||||||
chr11:117347955 | T | TTTG | 3 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0023c0023t0006g0034 |
3 | HG03834.hp2 HG04199.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.194+3705_194+3707d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117347955 | ||||||
chr11:117348046 | G | A | 34 | a0001c0005t0005g0004 a0001c0005t0005g0015 a0001c0005t0005g0035 others(31): Show |
37 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.195-3744G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348046 | |||||||
chr11:117348274 | G | C | 1 | a0015c0029t0012g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.195-3516G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348274 | |||||||
chr11:117348364 | C | T | 1 | a0003c0003t0004g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.195-3426C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348364 | |||||||
chr11:117348388 | G | A | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.195-3402G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348388 | |||||||
chr11:117348589 | G | C | 87 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(84): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.195-3201G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348589 | |||||||
chr11:117348672 | T | C | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.195-3118T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348672 | |||||||
chr11:117348756 | C | G | 3 | a0001c0005t0005g0269 a0001c0005t0005g0270 a0001c0005t0005g0271 |
3 | HG01168.hp2 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.195-3034C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117348756 | |||||||
chr11:117349054 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195-2736G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349054 | |||||||
chr11:117349085 | C | T | 6 | a0005c0007t0006g0259 a0005c0007t0006g0261 a0005c0007t0006g0264 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-2705C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349085 | |||||||
chr11:117349096 | C | T | 1 | a0002c0001t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195-2694C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349096 | |||||||
chr11:117349245 | A | G | 113 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(110): Show |
126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.195-2545A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349245 | |||||||
chr11:117349250 | C | T | 1 | a0002c0001t0009g0182 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195-2540C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349250 | |||||||
chr11:117349430 | G | T | 3 | a0001c0005t0005g0269 a0001c0005t0005g0270 a0001c0005t0005g0271 |
3 | HG01168.hp2 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.195-2360G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349430 | |||||||
chr11:117349608 | C | T | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-2182C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349608 | |||||||
chr11:117349713 | A | C | 1 | a0003c0003t0004g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.195-2077A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349713 | |||||||
chr11:117349884 | C | T | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-1906C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117349884 | |||||||
chr11:117350009 | G | A | 3 | a0001c0002t0002g0314 a0001c0002t0002g0315 a0001c0002t0002g0317 |
3 | NA18941.hp1 NA19010.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.195-1781G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350009 | |||||||
chr11:117350098 | G | A | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.195-1692G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350098 | |||||||
chr11:117350198 | C | T | 5 | a0001c0005t0005g0004 a0001c0005t0005g0015 a0001c0005t0005g0091 others(2): Show |
8 | NA18957.hp2 NA18970.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-1592C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350198 | |||||||
chr11:117350208 | CT | C | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.195-1570delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr11 | 117350208 | ||||||
chr11:117350277 | A | G | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.195-1513A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350277 | |||||||
chr11:117350412 | C | T | 1 | a0004c0008t0001g0297 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.195-1378C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350412 | |||||||
chr11:117350454 | T | G | 278 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(275): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.195-1336T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350454 | |||||||
chr11:117350508 | A | T | 1 | a0001c0026t0002g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.195-1282A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350508 | |||||||
chr11:117350667 | G | C | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-1123G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350667 | |||||||
chr11:117350754 | A | G | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.195-1036A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350754 | |||||||
chr11:117350852 | A | G | 4 | a0003c0003t0005g0086 a0003c0003t0005g0119 a0003c0003t0005g0120 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-938A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117350852 | |||||||
chr11:117351034 | T | G | 1 | a0004c0004t0001g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195-756T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351034 | |||||||
chr11:117351129 | T | G | 1 | a0001c0005t0005g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.195-661T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351129 | |||||||
chr11:117351146 | C | T | 2 | a0002c0001t0001g0005 a0002c0001t0001g0059 |
3 | HG01106.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.195-644C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351146 | |||||||
chr11:117351221 | G | C | 1 | a0002c0001t0003g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.195-569G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351221 | |||||||
chr11:117351259 | G | A | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-531G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351259 | |||||||
chr11:117351423 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.195-367C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351423 | |||||||
chr11:117351434 | C | T | 1 | a0010c0014t0013g0248 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.195-356C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351434 | |||||||
chr11:117351540 | T | C | 40 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0004g0072 others(37): Show |
46 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.195-250T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 4/32 | chr11 | 117351540 | |||||||
chr11:117352113 | G | A | 14 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(11): Show |
14 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+125G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352113 | |||||||
chr11:117352226 | G | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+238G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352226 | |||||||
chr11:117352290 | C | T | 1 | a0002c0001t0003g0212 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.393+302C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352290 | |||||||
chr11:117352481 | G | C | 8 | a0003c0003t0004g0101 a0003c0003t0004g0103 a0003c0003t0004g0115 others(5): Show |
8 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+493G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352481 | |||||||
chr11:117352481 | GTTCAAGA | G | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+496_393+502del others(7): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117352481 | ||||||
chr11:117352517 | A | G | 3 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0026c0018t0014g0263 |
3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.393+529A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352517 | |||||||
chr11:117352735 | C | T | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+747C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352735 | |||||||
chr11:117352743 | C | T | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+755C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352743 | |||||||
chr11:117352825 | G | C | 1 | a0025c0024t0005g0144 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.393+837G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352825 | |||||||
chr11:117352834 | G | A | 1 | a0004c0004t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.393+846G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352834 | |||||||
chr11:117352844 | C | T | 6 | a0005c0007t0006g0259 a0005c0007t0006g0261 a0005c0007t0006g0264 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+856C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352844 | |||||||
chr11:117352972 | T | A | 1 | a0002c0001t0003g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+984T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352972 | |||||||
chr11:117352976 | T | C | 355 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(352): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.393+988T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117352976 | |||||||
chr11:117353243 | C | T | 1 | a0003c0003t0004g0222 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.393+1255C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353243 | |||||||
chr11:117353290 | C | T | 14 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(11): Show |
14 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+1302C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353290 | |||||||
chr11:117353306 | C | T | 1 | a0014c0030t0021g0041 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.393+1318C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353306 | |||||||
chr11:117353434 | T | C | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+1446T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353434 | |||||||
chr11:117353644 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+1656G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353644 | |||||||
chr11:117353785 | G | A | 1 | a0002c0001t0001g0060 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+1797G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117353785 | |||||||
chr11:117353997 | TCTTCTC | T | 79 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.393+2015_393+2020d others(8): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117353997 | ||||||
chr11:117354003 | C | CCTT | 163 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(160): Show |
178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.393+2034_393+2036d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354003 | ||||||
chr11:117354003 | C | T | 1 | a0005c0007t0006g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.393+2015C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354003 | |||||||
chr11:117354072 | A | G | 4 | a0003c0003t0004g0007 a0003c0003t0004g0112 a0003c0003t0004g0113 others(1): Show |
5 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2084A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354072 | |||||||
chr11:117354102 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2114C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354102 | |||||||
chr11:117354127 | G | A | 1 | a0006c0006t0008g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.393+2139G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354127 | |||||||
chr11:117354136 | C | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+2148C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354136 | |||||||
chr11:117354162 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2174G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354162 | |||||||
chr11:117354171 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2183C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354171 | |||||||
chr11:117354178 | G | A | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.393+2190G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354178 | |||||||
chr11:117354204 | C | T | 5 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0005g0349 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2216C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354204 | |||||||
chr11:117354218 | A | G | 4 | a0002c0001t0001g0005 a0002c0001t0001g0059 a0002c0001t0001g0062 others(1): Show |
5 | HG00099.hp1 HG01106.hp1 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+2230A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354218 | |||||||
chr11:117354229 | G | T | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.393+2241G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354229 | |||||||
chr11:117354268 | G | A | 1 | a0001c0005t0005g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.393+2280G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354268 | |||||||
chr11:117354317 | T | C | 241 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(238): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.393+2329T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354317 | |||||||
chr11:117354418 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2430G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354418 | |||||||
chr11:117354496 | C | G | 1 | a0004c0004t0001g0296 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.393+2508C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354496 | |||||||
chr11:117354606 | C | A | 1 | a0002c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.393+2618C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354606 | |||||||
chr11:117354677 | T | G | 1 | a0001c0002t0002g0344 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.393+2689T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354677 | |||||||
chr11:117354725 | G | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2737G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354725 | |||||||
chr11:117354739 | T | A | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.393+2751T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354739 | |||||||
chr11:117354751 | T | A | 82 | a0001c0002t0004g0072 a0003c0003t0002g0131 a0003c0003t0004g0007 others(79): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+2763T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354751 | |||||||
chr11:117354766 | T | TTTTA | 7 | a0001c0002t0002g0039 a0001c0002t0002g0334 a0001c0002t0002g0335 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+2805_393+2808d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | ||||||
chr11:117354766 | T | TTTTATTT others(1): Show |
4 | a0001c0002t0002g0023 a0001c0002t0002g0333 a0001c0002t0002g0354 others(1): Show |
5 | HG00558.hp1 HG00621.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+2801_393+2808d others(10): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | ||||||
chr11:117354766 | TTTTA | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+2805_393+2808d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117354766 | ||||||
chr11:117354900 | C | T | 1 | a0002c0001t0001g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.393+2912C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117354900 | |||||||
chr11:117355101 | G | T | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+3113G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355101 | |||||||
chr11:117355266 | C | T | 34 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0011 others(31): Show |
40 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.393+3278C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355266 | |||||||
chr11:117355325 | A | G | 4 | a0001c0002t0002g0150 a0001c0002t0002g0151 a0001c0002t0002g0152 others(1): Show |
4 | HG00609.hp1 NA18940.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3337A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355325 | |||||||
chr11:117355529 | A | C | 4 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3541A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355529 | |||||||
chr11:117355546 | A | G | 2 | a0010c0014t0013g0181 a0010c0014t0013g0248 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+3558A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355546 | |||||||
chr11:117355677 | G | A | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.393+3689G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355677 | |||||||
chr11:117355814 | G | A | 1 | a0006c0006t0007g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.393+3826G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355814 | |||||||
chr11:117355900 | T | C | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+3912T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355900 | |||||||
chr11:117355903 | C | T | 23 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(20): Show |
24 | HG00408.hp1 HG01433.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.393+3915C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117355903 | |||||||
chr11:117355999 | G | GAGCAGCA others(2): Show |
80 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.393+4025_393+4033d others(11): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117355999 | ||||||
chr11:117355999 | G | GAGCAGCA others(11): Show |
1 | a0003c0003t0004g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+4016_393+4033d others(20): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117355999 | ||||||
chr11:117356049 | C | G | 1 | a0022c0035t0013g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+4061C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356049 | |||||||
chr11:117356057 | C | A | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+4069C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356057 | |||||||
chr11:117356133 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.393+4145C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356133 | |||||||
chr11:117356225 | T | A | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+4237T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356225 | |||||||
chr11:117356346 | C | T | 2 | a0001c0002t0002g0022 a0001c0002t0002g0347 |
3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.393+4358C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356346 | |||||||
chr11:117356657 | G | C | 1 | a0001c0026t0002g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.393+4669G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356657 | |||||||
chr11:117356673 | G | A | 1 | a0004c0004t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.393+4685G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356673 | |||||||
chr11:117356765 | C | T | 3 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0026c0018t0014g0263 |
3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.393+4777C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356765 | |||||||
chr11:117356803 | T | C | 192 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0002g0154 others(189): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.393+4815T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356803 | |||||||
chr11:117356869 | A | T | 4 | a0004c0008t0001g0293 a0004c0008t0001g0294 a0004c0008t0001g0295 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+4881A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356869 | |||||||
chr11:117356970 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-4865G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356970 | |||||||
chr11:117356978 | T | C | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-4857T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356978 | |||||||
chr11:117356994 | C | G | 2 | a0010c0014t0013g0181 a0010c0014t0013g0248 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.394-4841C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117356994 | |||||||
chr11:117357002 | A | G | 1 | a0004c0004t0001g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.394-4833A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357002 | |||||||
chr11:117357049 | T | A | 3 | a0001c0002t0002g0023 a0001c0002t0002g0333 a0001c0002t0002g0354 |
4 | HG00558.hp1 HG00621.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-4786T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357049 | |||||||
chr11:117357274 | T | A | 26 | a0001c0002t0003g0175 a0002c0001t0003g0069 a0002c0001t0003g0095 others(23): Show |
26 | HG00408.hp2 HG02040.hp1 NA18612.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-4561T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357274 | |||||||
chr11:117357356 | GCCTTGGC others(5): Show |
G | 6 | a0005c0007t0006g0259 a0005c0007t0006g0261 a0005c0007t0006g0264 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-4477_394-4466d others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357356 | ||||||
chr11:117357423 | C | CT | 77 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(74): Show |
87 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.394-4392dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | ||||||
chr11:117357423 | CTTTTTTT others(2): Show |
C | 63 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(60): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.394-4400_394-4392d others(11): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | ||||||
chr11:117357423 | CTTTTTTT others(3): Show |
C | 18 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(15): Show |
18 | HG00597.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-4401_394-4392d others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117357423 | ||||||
chr11:117357579 | A | G | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-4256A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357579 | |||||||
chr11:117357640 | T | A | 1 | a0001c0002t0002g0308 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-4195T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357640 | |||||||
chr11:117357644 | A | T | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-4191A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357644 | |||||||
chr11:117357659 | T | C | 4 | a0003c0003t0005g0086 a0003c0003t0005g0119 a0003c0003t0005g0120 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-4176T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357659 | |||||||
chr11:117357803 | A | G | 43 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(40): Show |
44 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.394-4032A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357803 | |||||||
chr11:117357948 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3887G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357948 | |||||||
chr11:117357977 | A | G | 1 | a0001c0002t0002g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.394-3858A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357977 | |||||||
chr11:117357993 | A | G | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3842A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117357993 | |||||||
chr11:117358133 | A | G | 25 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(22): Show |
29 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.394-3702A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358133 | |||||||
chr11:117358176 | G | A | 323 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(320): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.394-3659G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358176 | |||||||
chr11:117358402 | A | AAT | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-3433_394-3432i others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358402 | |||||||
chr11:117358540 | C | CT | 20 | a0002c0001t0003g0014 a0002c0001t0003g0097 a0002c0001t0003g0098 others(17): Show |
21 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.394-3277dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | ||||||
chr11:117358540 | C | CTT | 73 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-3278_394-3277d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | ||||||
chr11:117358540 | CT | C | 6 | a0001c0002t0002g0329 a0001c0005t0005g0270 a0002c0001t0001g0057 others(3): Show |
6 | HG01074.hp1 HG01168.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-3277delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358540 | ||||||
chr11:117358604 | T | C | 6 | a0004c0004t0001g0003 a0004c0004t0001g0050 a0004c0004t0001g0067 others(3): Show |
7 | NA18959.hp1 NA18989.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-3231T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358604 | |||||||
chr11:117358672 | A | G | 3 | a0002c0001t0001g0016 a0002c0001t0001g0276 a0002c0001t0001g0277 |
4 | NA18955.hp1 NA18957.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-3163A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358672 | |||||||
chr11:117358798 | G | A | 2 | a0007c0010t0002g0009 a0007c0010t0002g0156 |
3 | HG01074.hp2 HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.394-3037G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358798 | |||||||
chr11:117358833 | C | A | 1 | a0002c0001t0001g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.394-3002C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117358833 | |||||||
chr11:117358948 | C | CT | 86 | a0001c0005t0005g0173 a0002c0001t0003g0189 a0003c0003t0002g0131 others(83): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-2873dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117358948 | ||||||
chr11:117359031 | A | G | 2 | a0001c0002t0001g0311 a0001c0002t0001g0328 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-2804A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359031 | |||||||
chr11:117359117 | G | T | 77 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(74): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.394-2718G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359117 | |||||||
chr11:117359175 | C | T | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-2660C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359175 | |||||||
chr11:117359186 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-2649C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359186 | |||||||
chr11:117359235 | C | G | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394-2600C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359235 | |||||||
chr11:117359595 | C | T | 1 | a0001c0026t0002g0162 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-2240C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359595 | |||||||
chr11:117359882 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.394-1953A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117359882 | |||||||
chr11:117360150 | C | G | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394-1685C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360150 | |||||||
chr11:117360341 | T | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-1494T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360341 | |||||||
chr11:117360459 | C | T | 2 | a0002c0001t0001g0016 a0002c0001t0001g0277 |
3 | NA18957.hp1 NA18975.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.394-1376C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360459 | |||||||
chr11:117360475 | G | T | 1 | a0022c0035t0013g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.394-1360G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360475 | |||||||
chr11:117360703 | G | A | 5 | a0001c0002t0001g0043 a0001c0002t0001g0045 a0001c0002t0001g0046 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1132G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360703 | |||||||
chr11:117360895 | G | T | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-940G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360895 | |||||||
chr11:117360936 | C | CT | 109 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(106): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.394-883dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117360936 | ||||||
chr11:117360961 | G | T | 1 | a0001c0002t0002g0317 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.394-874G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117360961 | |||||||
chr11:117361027 | C | T | 1 | a0003c0003t0004g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.394-808C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361027 | |||||||
chr11:117361124 | A | G | 2 | a0002c0001t0003g0176 a0002c0001t0003g0177 |
2 | NA18967.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.394-711A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361124 | |||||||
chr11:117361233 | C | CT | 78 | a0001c0002t0001g0053 a0001c0002t0002g0021 a0001c0002t0002g0089 others(75): Show |
79 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.394-576dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | ||||||
chr11:117361233 | C | CTT | 8 | a0002c0001t0003g0192 a0002c0001t0003g0252 a0003c0003t0004g0123 others(5): Show |
8 | HG00423.hp1 HG01978.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-577_394-576dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | ||||||
chr11:117361233 | CT | C | 13 | a0001c0002t0001g0247 a0001c0002t0002g0047 a0001c0002t0002g0316 others(10): Show |
13 | HG01167.hp2 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-576delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | ||||||
chr11:117361233 | CTTTTTTT others(2): Show |
C | 2 | a0002c0001t0003g0001 a0002c0001t0003g0183 |
7 | HG00621.hp2 NA18945.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-584_394-576del others(9): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr11 | 117361233 | ||||||
chr11:117361309 | C | T | 1 | a0002c0001t0003g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.394-526C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361309 | |||||||
chr11:117361401 | C | T | 1 | a0001c0005t0005g0172 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-434C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361401 | |||||||
chr11:117361440 | C | G | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-395C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361440 | |||||||
chr11:117361484 | C | G | 2 | a0003c0003t0005g0008 a0003c0022t0005g0223 |
3 | HG01261.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.394-351C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361484 | |||||||
chr11:117361517 | G | A | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-318G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361517 | |||||||
chr11:117361544 | A | G | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-291A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361544 | |||||||
chr11:117361566 | A | G | 1 | a0026c0018t0014g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394-269A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361566 | |||||||
chr11:117361675 | A | G | 63 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(60): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.394-160A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361675 | |||||||
chr11:117361776 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.394-59C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 5/32 | chr11 | 117361776 | |||||||
chr11:117362087 | A | G | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.552+94A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362087 | |||||||
chr11:117362238 | A | G | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.553-166A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362238 | |||||||
chr11:117362316 | T | C | 1 | a0003c0003t0004g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.553-88T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362316 | |||||||
chr11:117362332 | G | A | 2 | a0004c0004t0001g0285 a0004c0004t0001g0286 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-72G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362332 | |||||||
chr11:117362393 | C | T | 2 | a0002c0001t0003g0211 a0002c0001t0003g0214 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.553-11C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 6/32 | chr11 | 117362393 | |||||||
chr11:117362662 | G | A | 1 | a0001c0002t0002g0356 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.687+124G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362662 | |||||||
chr11:117362711 | C | T | 76 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(73): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.687+173C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362711 | |||||||
chr11:117362723 | CT | C | 82 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(79): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.687+194delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr11 | 117362723 | ||||||
chr11:117362849 | A | G | 2 | a0003c0003t0005g0303 a0003c0003t0005g0322 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.687+311A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362849 | |||||||
chr11:117362920 | C | T | 1 | a0004c0009t0008g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.687+382C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117362920 | |||||||
chr11:117363122 | A | G | 1 | a0001c0002t0002g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.688-307A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117363122 | |||||||
chr11:117363347 | C | T | 2 | a0002c0001t0003g0176 a0002c0001t0003g0177 |
2 | NA18967.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.688-82C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 7/32 | chr11 | 117363347 | |||||||
chr11:117363646 | G | T | 2 | a0003c0003t0002g0131 a0003c0003t0004g0130 |
2 | NA18960.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.765+140G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363646 | |||||||
chr11:117363668 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.765+162A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363668 | |||||||
chr11:117363759 | C | CT | 88 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0045 others(85): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.765+281dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | C | CTT | 13 | a0001c0002t0001g0044 a0002c0001t0003g0177 a0002c0001t0003g0208 others(10): Show |
13 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.765+280_765+281dup others(2): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | C | CTTT | 42 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0077 others(39): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.765+279_765+281dup others(3): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | C | CTTTT | 9 | a0003c0003t0004g0055 a0003c0003t0004g0111 a0003c0003t0004g0134 others(6): Show |
9 | HG00741.hp1 HG01358.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.765+278_765+281dup others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | C | CTTTTT | 7 | a0003c0003t0004g0037 a0003c0003t0004g0038 a0003c0003t0004g0139 others(4): Show |
7 | HG00408.hp1 HG03453.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+277_765+281dup others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | CT | C | 14 | a0001c0002t0001g0247 a0001c0002t0002g0334 a0001c0005t0005g0323 others(11): Show |
14 | HG00323.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.765+281delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | CTTTTTTT | C | 10 | a0002c0001t0003g0001 a0002c0001t0003g0095 a0002c0001t0003g0183 others(7): Show |
15 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.765+275_765+281del others(7): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363759 | CTTTTTTT others(5): Show |
C | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+270_765+281del others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117363759 | ||||||
chr11:117363962 | C | A | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+456C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117363962 | |||||||
chr11:117364276 | G | A | 1 | a0002c0001t0003g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.765+770G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364276 | |||||||
chr11:117364565 | CT | C | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.765+1075delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117364565 | ||||||
chr11:117364649 | G | A | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+1143G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364649 | |||||||
chr11:117364652 | G | A | 67 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(64): Show |
72 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.765+1146G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364652 | |||||||
chr11:117364696 | C | T | 81 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(78): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.765+1190C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364696 | |||||||
chr11:117364744 | T | A | 1 | a0021c0033t0001g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.765+1238T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364744 | |||||||
chr11:117364893 | C | T | 1 | a0002c0001t0001g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+1387C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364893 | |||||||
chr11:117364931 | C | T | 78 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(75): Show |
88 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.765+1425C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117364931 | |||||||
chr11:117365031 | G | A | 7 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+1525G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365031 | |||||||
chr11:117365038 | G | A | 1 | a0004c0004t0001g0296 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.765+1532G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365038 | |||||||
chr11:117365151 | G | T | 1 | a0001c0005t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.765+1645G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365151 | |||||||
chr11:117365344 | C | T | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.765+1838C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365344 | |||||||
chr11:117365444 | T | A | 1 | a0004c0004t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.765+1938T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365444 | |||||||
chr11:117365496 | G | A | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.765+1990G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365496 | |||||||
chr11:117365522 | A | G | 4 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0025g0081 others(1): Show |
4 | HG01123.hp1 HG01346.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+2016A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365522 | |||||||
chr11:117365567 | A | ATTTC | 62 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(59): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.765+2081_765+2084d others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr11 | 117365567 | ||||||
chr11:117365603 | G | T | 66 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.765+2097G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365603 | |||||||
chr11:117365715 | G | A | 1 | a0002c0001t0003g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.765+2209G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365715 | |||||||
chr11:117365799 | C | T | 4 | a0003c0003t0004g0140 a0003c0003t0004g0141 a0003c0003t0004g0142 others(1): Show |
4 | HG00408.hp1 NA19002.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+2293C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365799 | |||||||
chr11:117365831 | C | T | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.765+2325C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365831 | |||||||
chr11:117365883 | A | C | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.765+2377A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117365883 | |||||||
chr11:117366200 | G | T | 1 | a0002c0001t0001g0017 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.765+2694G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366200 | |||||||
chr11:117366470 | G | A | 4 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(1): Show |
4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+2964G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366470 | |||||||
chr11:117366491 | C | G | 35 | a0004c0004t0001g0018 a0004c0004t0001g0019 a0004c0004t0001g0030 others(32): Show |
36 | HG00639.hp2 HG00738.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.765+2985C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366491 | |||||||
chr11:117366501 | C | T | 1 | a0008c0011t0012g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.765+2995C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366501 | |||||||
chr11:117366548 | C | A | 1 | a0001c0013t0005g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.765+3042C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366548 | |||||||
chr11:117366587 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.765+3081G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366587 | |||||||
chr11:117366620 | G | A | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+3114G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366620 | |||||||
chr11:117366639 | G | C | 3 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0029 |
3 | HG01884.hp1 HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.765+3133G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366639 | |||||||
chr11:117366771 | A | G | 82 | a0001c0002t0004g0072 a0003c0003t0002g0131 a0003c0003t0004g0007 others(79): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.765+3265A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366771 | |||||||
chr11:117366905 | A | G | 2 | a0003c0003t0004g0123 a0003c0003t0004g0225 |
2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.765+3399A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117366905 | |||||||
chr11:117367111 | G | A | 1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.765+3605G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367111 | |||||||
chr11:117367226 | C | T | 1 | a0001c0002t0002g0342 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.765+3720C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367226 | |||||||
chr11:117367395 | G | A | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766-3685G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367395 | |||||||
chr11:117367762 | G | A | 77 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(74): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-3318G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367762 | |||||||
chr11:117367775 | C | T | 85 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0004g0072 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-3305C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367775 | |||||||
chr11:117367810 | A | T | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3270A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117367810 | |||||||
chr11:117368281 | T | C | 1 | a0004c0009t0008g0026 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.766-2799T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368281 | |||||||
chr11:117368457 | A | C | 88 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0004g0072 others(85): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.766-2623A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368457 | |||||||
chr11:117368474 | G | T | 85 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0004g0072 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-2606G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368474 | |||||||
chr11:117368557 | C | T | 6 | a0001c0002t0002g0233 a0006c0006t0007g0051 a0006c0006t0007g0052 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-2523C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368557 | |||||||
chr11:117368618 | C | T | 9 | a0002c0001t0003g0001 a0002c0001t0003g0183 a0002c0001t0003g0184 others(6): Show |
14 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.766-2462C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368618 | |||||||
chr11:117368640 | C | T | 1 | a0002c0001t0003g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.766-2440C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117368640 | |||||||
chr11:117369046 | A | G | 1 | a0009c0020t0014g0321 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.766-2034A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369046 | |||||||
chr11:117369047 | T | C | 2 | a0001c0002t0002g0022 a0001c0002t0002g0347 |
3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.766-2033T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369047 | |||||||
chr11:117369068 | C | T | 1 | a0004c0004t0001g0291 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.766-2012C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369068 | |||||||
chr11:117369286 | C | T | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-1794C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369286 | |||||||
chr11:117369354 | A | G | 1 | a0004c0004t0001g0279 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766-1726A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369354 | |||||||
chr11:117369498 | G | T | 5 | a0001c0002t0001g0053 a0001c0002t0001g0246 a0001c0002t0001g0247 others(2): Show |
5 | HG01069.hp2 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-1582G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369498 | |||||||
chr11:117369641 | G | A | 85 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0004g0072 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.766-1439G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117369641 | |||||||
chr11:117370132 | C | T | 1 | a0001c0002t0002g0308 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-948C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370132 | |||||||
chr11:117370134 | T | C | 1 | a0026c0018t0014g0263 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766-946T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370134 | |||||||
chr11:117370331 | A | G | 1 | a0003c0003t0004g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.766-749A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370331 | |||||||
chr11:117370437 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.766-643A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370437 | |||||||
chr11:117370499 | C | T | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-581C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370499 | |||||||
chr11:117370598 | G | A | 1 | a0002c0001t0001g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.766-482G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370598 | |||||||
chr11:117370681 | C | T | 1 | a0002c0001t0003g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.766-399C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370681 | |||||||
chr11:117370682 | G | A | 1 | a0002c0001t0003g0013 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.766-398G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370682 | |||||||
chr11:117370713 | C | T | 42 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0002c0001t0001g0056 others(39): Show |
43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.766-367C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370713 | |||||||
chr11:117370939 | G | A | 1 | a0006c0006t0007g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-141G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117370939 | |||||||
chr11:117371012 | T | C | 2 | a0004c0004t0001g0030 a0004c0004t0001g0306 |
2 | NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766-68T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117371012 | |||||||
chr11:117371044 | T | A | 192 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0003g0175 others(189): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.766-36T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 8/32 | chr11 | 117371044 | |||||||
chr11:117371763 | C | T | 1 | a0001c0005t0005g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1152+297C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117371763 | |||||||
chr11:117371795 | C | CT | 234 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(231): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1152+344dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117371795 | ||||||
chr11:117371795 | C | CTT | 9 | a0002c0001t0001g0057 a0002c0001t0003g0177 a0003c0003t0004g0037 others(6): Show |
9 | HG00738.hp1 HG01358.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1152+343_1152+344d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117371795 | ||||||
chr11:117372050 | A | T | 1 | a0003c0003t0005g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1152+584A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372050 | |||||||
chr11:117372108 | A | AT | 57 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(54): Show |
58 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1152+659dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | ||||||
chr11:117372108 | A | ATT | 79 | a0002c0001t0001g0075 a0002c0001t0001g0093 a0003c0003t0002g0131 others(76): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1152+658_1152+659d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | ||||||
chr11:117372108 | A | ATTT | 99 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0002g0047 others(96): Show |
112 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1152+657_1152+659d others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372108 | ||||||
chr11:117372299 | C | T | 1 | a0002c0001t0003g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1152+833C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372299 | |||||||
chr11:117372373 | A | C | 1 | a0003c0003t0004g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1152+907A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372373 | |||||||
chr11:117372423 | C | CT | 14 | a0004c0004t0001g0281 a0004c0004t0001g0282 a0004c0004t0001g0283 others(11): Show |
14 | HG00639.hp2 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+968dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117372423 | ||||||
chr11:117372480 | C | T | 1 | a0001c0002t0022g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1152+1014C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372480 | |||||||
chr11:117372501 | C | T | 9 | a0002c0001t0003g0001 a0002c0001t0003g0183 a0002c0001t0003g0184 others(6): Show |
14 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1152+1035C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117372501 | |||||||
chr11:117373013 | T | C | 3 | a0002c0001t0003g0201 a0002c0001t0003g0202 a0002c0001t0003g0204 |
3 | NA18946.hp2 NA19078.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1153-738T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373013 | |||||||
chr11:117373037 | A | G | 4 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0025g0081 others(1): Show |
4 | HG01123.hp1 HG01346.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-714A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373037 | |||||||
chr11:117373107 | G | A | 3 | a0001c0002t0002g0314 a0002c0001t0003g0137 a0002c0001t0003g0138 |
3 | HG02809.hp1 HG03516.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1153-644G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373107 | |||||||
chr11:117373323 | C | T | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-428C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373323 | |||||||
chr11:117373363 | GA | G | 9 | a0001c0002t0001g0320 a0001c0002t0002g0160 a0001c0002t0002g0314 others(6): Show |
9 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1153-375delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr11 | 117373363 | ||||||
chr11:117373456 | C | A | 2 | a0002c0001t0003g0185 a0002c0001t0003g0186 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1153-295C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373456 | |||||||
chr11:117373539 | C | A | 10 | a0002c0001t0001g0005 a0002c0001t0001g0056 a0002c0001t0001g0057 others(7): Show |
11 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1153-212C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373539 | |||||||
chr11:117373575 | C | T | 4 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(1): Show |
4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-176C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373575 | |||||||
chr11:117373577 | T | C | 5 | a0001c0002t0001g0320 a0001c0002t0002g0160 a0001c0002t0002g0314 others(2): Show |
5 | NA18941.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-174T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373577 | |||||||
chr11:117373609 | C | T | 1 | a0002c0001t0001g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1153-142C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373609 | |||||||
chr11:117373663 | C | T | 1 | a0006c0006t0007g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1153-88C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 9/32 | chr11 | 117373663 | |||||||
chr11:117373890 | A | T | 4 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(1): Show |
4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+59A>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117373890 | |||||||
chr11:117373931 | G | A | 2 | a0003c0003t0004g0123 a0003c0003t0004g0225 |
2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1233+100G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117373931 | |||||||
chr11:117374299 | G | A | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1233+468G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374299 | |||||||
chr11:117374417 | C | T | 126 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(123): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1233+586C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374417 | |||||||
chr11:117374575 | G | A | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1233+744G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374575 | |||||||
chr11:117374780 | G | A | 1 | a0009c0020t0014g0321 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1234-928G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117374780 | |||||||
chr11:117375008 | C | T | 1 | a0001c0002t0002g0021 | 2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1234-700C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375008 | |||||||
chr11:117375102 | G | C | 1 | a0016c0025t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1234-606G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375102 | |||||||
chr11:117375272 | C | T | 36 | a0001c0002t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0010 others(33): Show |
42 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1234-436C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375272 | |||||||
chr11:117375326 | G | A | 1 | a0001c0002t0002g0315 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1234-382G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375326 | |||||||
chr11:117375349 | G | A | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1234-359G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375349 | |||||||
chr11:117375434 | T | C | 153 | a0001c0002t0003g0175 a0001c0002t0004g0072 a0002c0001t0003g0001 others(150): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1234-274T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375434 | |||||||
chr11:117375687 | T | G | 3 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0026c0018t0014g0263 |
3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1234-21T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 10/32 | chr11 | 117375687 | |||||||
chr11:117375850 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1317+59G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117375850 | |||||||
chr11:117376160 | T | C | 37 | a0002c0001t0001g0005 a0002c0001t0001g0016 a0002c0001t0001g0017 others(34): Show |
43 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1317+369T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376160 | |||||||
chr11:117376199 | C | G | 1 | a0006c0006t0007g0080 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1317+408C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376199 | |||||||
chr11:117376246 | T | A | 1 | a0024c0028t0004g0163 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1317+455T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376246 | |||||||
chr11:117376248 | GTCCTGGA others(17): Show |
G | 1 | a0004c0004t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1317+462_1317+485d others(26): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117376248 | ||||||
chr11:117376312 | C | T | 1 | a0002c0001t0003g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1317+521C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376312 | |||||||
chr11:117376510 | A | G | 2 | a0003c0003t0005g0303 a0003c0003t0005g0322 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1317+719A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376510 | |||||||
chr11:117376595 | CCAGCCTT others(29): Show |
C | 7 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317+844_1317+879d others(38): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117376595 | ||||||
chr11:117376829 | G | A | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1317+1038G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376829 | |||||||
chr11:117376885 | A | G | 1 | a0005c0007t0006g0032 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1317+1094A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117376885 | |||||||
chr11:117377048 | G | A | 1 | a0004c0004t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1317+1257G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377048 | |||||||
chr11:117377048 | G | C | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1317+1257G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377048 | |||||||
chr11:117377187 | C | CCA | 237 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(234): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1317+1397_1317+139 others(6): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117377187 | ||||||
chr11:117377418 | T | C | 2 | a0003c0003t0005g0008 a0003c0022t0005g0223 |
3 | HG01261.hp2 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1317+1627T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377418 | |||||||
chr11:117377509 | G | C | 1 | a0002c0001t0003g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1317+1718G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377509 | |||||||
chr11:117377517 | G | A | 6 | a0001c0002t0002g0039 a0001c0002t0002g0334 a0001c0002t0002g0335 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317+1726G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377517 | |||||||
chr11:117377552 | G | A | 63 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(60): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1317+1761G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377552 | |||||||
chr11:117377626 | G | A | 4 | a0001c0002t0002g0002 a0001c0002t0002g0147 a0001c0002t0002g0157 others(1): Show |
7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317+1835G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377626 | |||||||
chr11:117377635 | A | G | 4 | a0001c0002t0002g0020 a0001c0002t0002g0344 a0001c0002t0002g0346 others(1): Show |
5 | HG01952.hp1 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1317+1844A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377635 | |||||||
chr11:117377698 | C | A | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1317+1907C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377698 | |||||||
chr11:117377942 | C | T | 6 | a0005c0007t0006g0259 a0005c0007t0006g0261 a0005c0007t0006g0264 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317+2151C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377942 | |||||||
chr11:117377969 | C | T | 1 | a0001c0002t0002g0341 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1317+2178C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117377969 | |||||||
chr11:117378021 | C | T | 1 | a0002c0001t0001g0017 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1317+2230C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378021 | |||||||
chr11:117378115 | C | T | 1 | a0001c0002t0002g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1317+2324C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378115 | |||||||
chr11:117378116 | G | A | 17 | a0002c0001t0001g0005 a0002c0001t0001g0056 a0002c0001t0001g0057 others(14): Show |
19 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1317+2325G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378116 | |||||||
chr11:117378171 | C | G | 1 | a0002c0001t0003g0249 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1317+2380C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378171 | |||||||
chr11:117378268 | C | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1318-2346C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378268 | |||||||
chr11:117378360 | C | CT | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318-2248dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117378360 | ||||||
chr11:117378402 | G | T | 1 | a0001c0005t0005g0168 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1318-2212G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378402 | |||||||
chr11:117378857 | C | G | 1 | a0002c0001t0001g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1318-1757C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117378857 | |||||||
chr11:117379170 | G | A | 1 | a0004c0004t0001g0296 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1318-1444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379170 | |||||||
chr11:117379411 | C | T | 1 | a0001c0005t0005g0244 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1318-1203C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379411 | |||||||
chr11:117379703 | T | G | 1 | a0002c0001t0001g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1318-911T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379703 | |||||||
chr11:117379709 | G | T | 1 | a0003c0003t0004g0055 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1318-905G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379709 | |||||||
chr11:117379814 | G | A | 2 | a0003c0003t0004g0129 a0003c0003t0004g0133 |
2 | HG00099.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1318-800G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117379814 | |||||||
chr11:117379852 | C | CT | 141 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(138): Show |
156 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1318-739dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | ||||||
chr11:117379852 | C | CTT | 9 | a0001c0002t0002g0020 a0001c0002t0002g0344 a0001c0002t0002g0346 others(6): Show |
10 | HG01361.hp2 HG01433.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1318-740_1318-739d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | ||||||
chr11:117379852 | CT | C | 30 | a0001c0005t0005g0090 a0001c0005t0005g0091 a0001c0005t0005g0168 others(27): Show |
31 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.1318-739delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr11 | 117379852 | ||||||
chr11:117380033 | C | T | 10 | a0004c0004t0001g0018 a0004c0004t0001g0019 a0004c0004t0001g0279 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1318-581C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380033 | |||||||
chr11:117380170 | G | A | 1 | a0002c0001t0003g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1318-444G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380170 | |||||||
chr11:117380221 | C | T | 2 | a0003c0003t0005g0303 a0003c0003t0005g0322 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1318-393C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380221 | |||||||
chr11:117380427 | A | G | 166 | a0001c0002t0003g0175 a0002c0001t0001g0005 a0002c0001t0001g0056 others(163): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1318-187A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380427 | |||||||
chr11:117380503 | C | A | 13 | a0004c0004t0001g0018 a0004c0004t0001g0019 a0004c0004t0001g0279 others(10): Show |
14 | HG01081.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1318-111C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 11/32 | chr11 | 117380503 | |||||||
chr11:117380786 | C | T | 1 | a0003c0003t0004g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1409+81C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380786 | |||||||
chr11:117380805 | G | C | 322 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(319): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1409+100G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380805 | |||||||
chr11:117380851 | C | T | 1 | a0001c0002t0002g0346 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1409+146C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380851 | |||||||
chr11:117380867 | G | A | 1 | a0013c0019t0004g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1409+162G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380867 | |||||||
chr11:117380897 | T | G | 1 | a0002c0001t0003g0205 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1409+192T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117380897 | |||||||
chr11:117381105 | T | G | 1 | a0001c0002t0005g0240 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1409+400T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381105 | |||||||
chr11:117381324 | C | T | 2 | a0009c0021t0019g0085 a0019c0032t0020g0191 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1410-377C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381324 | |||||||
chr11:117381371 | C | T | 3 | a0002c0001t0003g0210 a0002c0001t0003g0211 a0002c0001t0003g0214 |
3 | HG01069.hp1 HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1410-330C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381371 | |||||||
chr11:117381419 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1410-282G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381419 | |||||||
chr11:117381519 | A | C | 2 | a0003c0003t0005g0303 a0003c0003t0005g0322 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1410-182A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381519 | |||||||
chr11:117381609 | A | G | 1 | a0024c0028t0004g0163 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1410-92A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 12/32 | chr11 | 117381609 | |||||||
chr11:117382245 | T | G | 1 | a0003c0003t0004g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1577+377T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382245 | |||||||
chr11:117382514 | C | T | 4 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(1): Show |
4 | HG01884.hp1 HG02683.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578-282C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382514 | |||||||
chr11:117382556 | G | A | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1578-240G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382556 | |||||||
chr11:117382764 | T | C | 1 | a0002c0001t0003g0200 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1578-32T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 13/32 | chr11 | 117382764 | |||||||
chr11:117383013 | T | C | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1724+71T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383013 | |||||||
chr11:117383352 | T | C | 1 | a0001c0036t0005g0170 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1724+410T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383352 | |||||||
chr11:117383406 | G | A | 13 | a0002c0001t0001g0005 a0002c0001t0001g0056 a0002c0001t0001g0057 others(10): Show |
14 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1724+464G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383406 | |||||||
chr11:117383896 | C | T | 1 | a0002c0001t0001g0017 | 2 | NA18966.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1724+954C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383896 | |||||||
chr11:117383973 | T | G | 1 | a0004c0004t0001g0068 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1724+1031T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117383973 | |||||||
chr11:117384483 | T | C | 1 | a0003c0022t0005g0223 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1724+1541T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384483 | |||||||
chr11:117384567 | C | T | 17 | a0001c0002t0001g0053 a0001c0002t0001g0073 a0001c0002t0001g0074 others(14): Show |
19 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1724+1625C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384567 | |||||||
chr11:117384607 | C | A | 3 | a0002c0001t0003g0216 a0002c0001t0003g0217 a0002c0001t0003g0218 |
3 | HG00438.hp1 HG00558.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.1724+1665C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384607 | |||||||
chr11:117384670 | C | T | 2 | a0004c0015t0003g0027 a0004c0015t0003g0028 |
2 | HG00323.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1724+1728C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384670 | |||||||
chr11:117384921 | C | T | 1 | a0002c0001t0003g0200 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1724+1979C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384921 | |||||||
chr11:117384966 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1724+2024T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384966 | |||||||
chr11:117384971 | G | A | 2 | a0002c0001t0003g0211 a0002c0001t0003g0214 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1724+2029G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117384971 | |||||||
chr11:117385121 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1725-2082G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385121 | |||||||
chr11:117385134 | C | T | 1 | a0007c0010t0002g0009 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1725-2069C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385134 | |||||||
chr11:117385171 | C | T | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1725-2032C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385171 | |||||||
chr11:117385412 | G | A | 1 | a0001c0005t0005g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1725-1791G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385412 | |||||||
chr11:117385414 | G | A | 1 | a0001c0002t0002g0234 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1725-1789G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385414 | |||||||
chr11:117385509 | T | C | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1694T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385509 | |||||||
chr11:117385650 | G | A | 1 | a0002c0001t0001g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1725-1553G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385650 | |||||||
chr11:117385668 | C | G | 186 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(183): Show |
200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1725-1535C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385668 | |||||||
chr11:117385720 | T | C | 140 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0011 others(137): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1725-1483T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385720 | |||||||
chr11:117385763 | G | C | 1 | a0003c0003t0004g0128 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1725-1440G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385763 | |||||||
chr11:117385864 | A | G | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1339A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385864 | |||||||
chr11:117385973 | T | G | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1725-1230T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117385973 | |||||||
chr11:117386367 | G | A | 3 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0026c0018t0014g0263 |
3 | HG02559.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1725-836G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386367 | |||||||
chr11:117386462 | A | G | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1725-741A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386462 | |||||||
chr11:117386705 | T | G | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1725-498T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386705 | |||||||
chr11:117386860 | A | G | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1725-343A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117386860 | |||||||
chr11:117387015 | A | G | 1 | a0005c0007t0006g0032 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1725-188A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387015 | |||||||
chr11:117387117 | G | A | 1 | a0001c0002t0001g0320 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1725-86G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387117 | |||||||
chr11:117387160 | G | T | 74 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(71): Show |
84 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1725-43G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 14/32 | chr11 | 117387160 | |||||||
chr11:117387482 | T | C | 120 | a0001c0002t0003g0175 a0002c0001t0001g0005 a0002c0001t0001g0016 others(117): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1934+70T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387482 | |||||||
chr11:117387929 | A | C | 5 | a0001c0002t0001g0320 a0001c0002t0002g0160 a0001c0002t0002g0314 others(2): Show |
5 | NA18941.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1934+517A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387929 | |||||||
chr11:117387946 | C | G | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1934+534C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387946 | |||||||
chr11:117387971 | G | T | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1934+559G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117387971 | |||||||
chr11:117388218 | G | C | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1934+806G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388218 | |||||||
chr11:117388471 | T | G | 1 | a0001c0005t0005g0173 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1934+1059T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388471 | |||||||
chr11:117388479 | C | T | 1 | a0001c0005t0005g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1934+1067C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388479 | |||||||
chr11:117388771 | CT | C | 201 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(198): Show |
218 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1934+1373delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117388771 | ||||||
chr11:117388834 | C | T | 1 | a0004c0004t0001g0296 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1934+1422C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388834 | |||||||
chr11:117388910 | C | T | 2 | a0004c0004t0001g0309 a0004c0004t0001g0310 |
2 | HG02155.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1934+1498C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388910 | |||||||
chr11:117388939 | T | A | 1 | a0003c0003t0005g0322 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1934+1527T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388939 | |||||||
chr11:117388940 | T | TA | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1934+1528_1934+152 others(5): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117388940 | |||||||
chr11:117389022 | G | C | 4 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1934+1610G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389022 | |||||||
chr11:117389066 | G | A | 29 | a0002c0001t0003g0069 a0002c0001t0003g0095 a0002c0001t0003g0099 others(26): Show |
29 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1934+1654G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389066 | |||||||
chr11:117389188 | C | T | 2 | a0004c0004t0001g0281 a0004c0004t0001g0282 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1935-1589C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389188 | |||||||
chr11:117389223 | C | T | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1935-1554C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389223 | |||||||
chr11:117389359 | A | G | 118 | a0002c0001t0001g0005 a0002c0001t0001g0016 a0002c0001t0001g0017 others(115): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1935-1418A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389359 | |||||||
chr11:117389464 | G | T | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935-1313G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389464 | |||||||
chr11:117389553 | C | T | 1 | a0001c0005t0005g0036 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935-1224C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389553 | |||||||
chr11:117389788 | G | A | 74 | a0002c0001t0003g0001 a0002c0001t0003g0012 a0002c0001t0003g0014 others(71): Show |
81 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1935-989G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389788 | |||||||
chr11:117389926 | G | A | 2 | a0001c0002t0002g0159 a0002c0001t0001g0066 |
2 | HG02040.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1935-851G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117389926 | |||||||
chr11:117389938 | C | CT | 19 | a0001c0002t0002g0148 a0001c0002t0002g0231 a0001c0002t0002g0234 others(16): Show |
20 | HG00423.hp2 HG01106.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.1935-818dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | ||||||
chr11:117389938 | CT | C | 165 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0045 others(162): Show |
179 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1935-818delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | ||||||
chr11:117389938 | CTT | C | 10 | a0001c0002t0001g0053 a0001c0002t0001g0073 a0001c0002t0001g0074 others(7): Show |
10 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935-819_1935-818d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117389938 | ||||||
chr11:117390001 | G | A | 1 | a0011c0012t0006g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1935-776G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390001 | |||||||
chr11:117390034 | C | T | 1 | a0001c0002t0005g0240 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1935-743C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390034 | |||||||
chr11:117390085 | G | A | 1 | a0003c0003t0004g0104 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1935-692G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390085 | |||||||
chr11:117390235 | G | C | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1935-542G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390235 | |||||||
chr11:117390285 | C | T | 1 | a0001c0005t0005g0058 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1935-492C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390285 | |||||||
chr11:117390299 | G | T | 1 | a0002c0001t0003g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-478G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390299 | |||||||
chr11:117390310 | G | A | 1 | a0002c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1935-467G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390310 | |||||||
chr11:117390558 | C | A | 1 | a0002c0001t0003g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-219C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390558 | |||||||
chr11:117390642 | GA | G | 75 | a0002c0001t0003g0001 a0002c0001t0003g0012 a0002c0001t0003g0014 others(72): Show |
82 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1935-120delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr11 | 117390642 | ||||||
chr11:117390643 | A | G | 1 | a0002c0001t0003g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1935-134A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390643 | |||||||
chr11:117390772 | C | G | 39 | a0003c0003t0002g0131 a0003c0003t0004g0007 a0003c0003t0004g0037 others(36): Show |
40 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.1935-5C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 15/32 | chr11 | 117390772 | |||||||
chr11:117390970 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2067-29C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 16/32 | chr11 | 117390970 | |||||||
chr11:117391238 | T | A | 1 | a0008c0011t0007g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2283+23T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391238 | |||||||
chr11:117391436 | A | C | 1 | a0002c0001t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2283+221A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391436 | |||||||
chr11:117391668 | C | G | 1 | a0001c0002t0002g0315 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2283+453C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391668 | |||||||
chr11:117391742 | G | A | 3 | a0010c0014t0013g0181 a0010c0014t0013g0248 a0022c0035t0013g0049 |
3 | HG02630.hp1 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-484G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391742 | |||||||
chr11:117391882 | C | T | 94 | a0002c0001t0003g0001 a0002c0001t0003g0012 a0002c0001t0003g0013 others(91): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2284-344C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391882 | |||||||
chr11:117391981 | G | A | 1 | a0002c0001t0003g0198 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2284-245G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117391981 | |||||||
chr11:117392068 | G | T | 1 | a0002c0001t0003g0200 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2284-158G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117392068 | |||||||
chr11:117392151 | A | G | 2 | a0003c0003t0011g0122 a0003c0003t0011g0126 |
2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2284-75A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 17/32 | chr11 | 117392151 | |||||||
chr11:117392387 | T | C | 86 | a0002c0001t0003g0001 a0002c0001t0003g0012 a0002c0001t0003g0013 others(83): Show |
94 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2361+84T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 18/32 | chr11 | 117392387 | |||||||
chr11:117392655 | G | C | 1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2493+28G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392655 | |||||||
chr11:117392833 | G | A | 1 | a0016c0025t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2494-171G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392833 | |||||||
chr11:117392900 | T | G | 86 | a0002c0001t0003g0001 a0002c0001t0003g0012 a0002c0001t0003g0013 others(83): Show |
94 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2494-104T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 19/32 | chr11 | 117392900 | |||||||
chr11:117393155 | G | GCACACAC others(5): Show |
2 | a0002c0001t0003g0211 a0002c0001t0003g0214 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2616+43_2616+54dup others(12): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | INFO_REALIGN_3_PRIME | chr11 | 117393155 | ||||||
chr11:117393158 | C | T | 3 | a0007c0010t0002g0009 a0007c0010t0002g0156 a0007c0010t0002g0179 |
4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616+32C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393158 | |||||||
chr11:117393204 | C | T | 1 | a0006c0006t0007g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2616+78C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393204 | |||||||
chr11:117393486 | C | T | 5 | a0003c0003t0004g0107 a0003c0003t0004g0108 a0003c0003t0004g0109 others(2): Show |
5 | HG02698.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616+360C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393486 | |||||||
chr11:117393540 | G | A | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616+414G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393540 | |||||||
chr11:117393742 | T | C | 4 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2617-608T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117393742 | |||||||
chr11:117394258 | C | T | 2 | a0003c0003t0004g0108 a0003c0003t0004g0111 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2617-92C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394258 | |||||||
chr11:117394298 | T | C | 1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2617-52T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394298 | |||||||
chr11:117394328 | G | A | 1 | a0003c0003t0004g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2617-22G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394328 | |||||||
chr11:117394332 | G | A | 1 | a0007c0010t0002g0009 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2617-18G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 20/32 | chr11 | 117394332 | |||||||
chr11:117395067 | G | T | 1 | a0021c0033t0001g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2845-56G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 22/32 | chr11 | 117395067 | |||||||
chr11:117395350 | C | T | 2 | a0008c0011t0012g0083 a0008c0011t0012g0084 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2913+159C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395350 | |||||||
chr11:117395378 | G | A | 79 | a0002c0001t0001g0005 a0002c0001t0001g0056 a0002c0001t0001g0057 others(76): Show |
88 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2914-169G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395378 | |||||||
chr11:117395479 | G | A | 1 | a0002c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2914-68G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 23/32 | chr11 | 117395479 | |||||||
chr11:117395750 | T | C | 14 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(11): Show |
14 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.3089+28T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395750 | |||||||
chr11:117395932 | G | C | 116 | a0001c0002t0003g0175 a0002c0001t0001g0005 a0002c0001t0001g0016 others(113): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.3090-122G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395932 | |||||||
chr11:117395938 | T | C | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3090-116T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117395938 | |||||||
chr11:117396006 | C | A | 1 | a0001c0002t0002g0329 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3090-48C>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396006 | |||||||
chr11:117396006 | C | G | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3090-48C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396006 | |||||||
chr11:117396038 | A | C | 187 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(184): Show |
201 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.3090-16A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 24/32 | chr11 | 117396038 | |||||||
chr11:117396185 | GCTGGGGG others(7): Show |
G | 1 | a0001c0002t0023g0241 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3216+20_3216+33del others(14): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr11 | 117396185 | ||||||
chr11:117396721 | G | T | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3278+110G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117396721 | |||||||
chr11:117396924 | C | T | 1 | a0001c0005t0005g0171 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3279-167C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117396924 | |||||||
chr11:117397056 | G | T | 1 | a0002c0001t0024g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3279-35G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 26/32 | chr11 | 117397056 | |||||||
chr11:117397358 | C | G | 28 | a0002c0001t0003g0069 a0002c0001t0003g0095 a0002c0001t0003g0174 others(25): Show |
28 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3501+45C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397358 | |||||||
chr11:117397540 | G | T | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3501+227G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397540 | |||||||
chr11:117397740 | C | T | 2 | a0010c0014t0013g0181 a0010c0014t0013g0248 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3501+427C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397740 | |||||||
chr11:117397820 | G | A | 1 | a0001c0005t0005g0349 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3501+507G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397820 | |||||||
chr11:117397826 | C | T | 1 | a0001c0002t0002g0334 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3501+513C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397826 | |||||||
chr11:117397880 | C | G | 3 | a0002c0001t0003g0210 a0002c0001t0003g0211 a0002c0001t0003g0214 |
3 | HG01069.hp1 HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.3501+567C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397880 | |||||||
chr11:117397923 | C | T | 1 | a0004c0004t0001g0282 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3501+610C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397923 | |||||||
chr11:117397966 | T | C | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+653T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397966 | |||||||
chr11:117397967 | T | C | 44 | a0001c0002t0001g0053 a0001c0002t0001g0073 a0001c0002t0001g0074 others(41): Show |
50 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.3501+654T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117397967 | |||||||
chr11:117398316 | A | C | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1003A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398316 | |||||||
chr11:117398375 | T | C | 4 | a0001c0002t0002g0002 a0001c0002t0002g0147 a0001c0002t0002g0157 others(1): Show |
7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3501+1062T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398375 | |||||||
chr11:117398526 | C | T | 5 | a0002c0001t0009g0182 a0002c0001t0009g0190 a0002c0001t0009g0250 others(2): Show |
5 | HG01074.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3501+1213C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398526 | |||||||
chr11:117398553 | T | A | 12 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(9): Show |
12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.3501+1240T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398553 | |||||||
chr11:117398585 | C | CT | 12 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(9): Show |
12 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.3501+1274dupT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117398585 | ||||||
chr11:117398629 | T | G | 1 | a0001c0005t0005g0171 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3501+1316T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398629 | |||||||
chr11:117398640 | G | A | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1327G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117398640 | |||||||
chr11:117399061 | G | A | 5 | a0006c0006t0007g0051 a0006c0006t0007g0052 a0006c0006t0007g0078 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3501+1748G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399061 | |||||||
chr11:117399107 | G | A | 1 | a0001c0002t0005g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3501+1794G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399107 | |||||||
chr11:117399126 | C | T | 3 | a0007c0010t0002g0009 a0007c0010t0002g0156 a0007c0010t0002g0179 |
4 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+1813C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399126 | |||||||
chr11:117399684 | A | G | 1 | a0001c0002t0002g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3501+2371A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399684 | |||||||
chr11:117399746 | CT | C | 10 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(7): Show |
10 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.3501+2442delT | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117399746 | ||||||
chr11:117399908 | T | G | 1 | a0022c0035t0013g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3501+2595T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117399908 | |||||||
chr11:117400102 | A | C | 109 | a0001c0002t0003g0175 a0002c0001t0001g0005 a0002c0001t0001g0016 others(106): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.3501+2789A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400102 | |||||||
chr11:117400575 | G | A | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+3262G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400575 | |||||||
chr11:117400713 | G | A | 1 | a0002c0001t0003g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3501+3400G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400713 | |||||||
chr11:117400783 | C | T | 322 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(319): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.3501+3470C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117400783 | |||||||
chr11:117401137 | T | C | 1 | a0002c0001t0003g0195 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3501+3824T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401137 | |||||||
chr11:117401214 | C | T | 2 | a0009c0020t0014g0321 a0026c0018t0014g0263 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3501+3901C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401214 | |||||||
chr11:117401290 | T | C | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.3501+3977T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401290 | |||||||
chr11:117401531 | G | T | 2 | a0009c0021t0019g0085 a0019c0032t0020g0191 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3501+4218G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401531 | |||||||
chr11:117401970 | C | G | 1 | a0001c0005t0005g0323 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3501+4657C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117401970 | |||||||
chr11:117402223 | G | T | 91 | a0001c0013t0005g0232 a0002c0001t0001g0016 a0002c0001t0001g0017 others(88): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3501+4910G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402223 | |||||||
chr11:117402335 | T | C | 326 | a0001c0002t0001g0040 a0001c0002t0001g0043 a0001c0002t0001g0044 others(323): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.3501+5022T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402335 | |||||||
chr11:117402378 | G | T | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3501+5065G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402378 | |||||||
chr11:117402423 | G | A | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3501+5110G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402423 | |||||||
chr11:117402437 | T | C | 2 | a0009c0021t0019g0085 a0019c0032t0020g0191 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3501+5124T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402437 | |||||||
chr11:117402453 | T | C | 3 | a0004c0034t0007g0042 a0008c0011t0007g0031 a0014c0030t0021g0041 |
3 | HG02145.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3501+5140T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402453 | |||||||
chr11:117402467 | G | T | 5 | a0002c0001t0003g0137 a0002c0001t0003g0138 a0002c0001t0003g0195 others(2): Show |
5 | HG02809.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3501+5154G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402467 | |||||||
chr11:117402546 | C | T | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3501+5233C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402546 | |||||||
chr11:117402870 | T | G | 1 | a0004c0004t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3502-5055T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402870 | |||||||
chr11:117402913 | C | T | 1 | a0004c0004t0001g0291 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3502-5012C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402913 | |||||||
chr11:117402943 | A | G | 6 | a0005c0007t0006g0259 a0005c0007t0006g0261 a0005c0007t0006g0264 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-4982A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402943 | |||||||
chr11:117402953 | G | A | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3502-4972G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117402953 | |||||||
chr11:117403117 | T | C | 2 | a0001c0002t0002g0089 a0001c0002t0003g0175 |
2 | HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.3502-4808T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403117 | |||||||
chr11:117403215 | T | A | 1 | a0001c0002t0022g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3502-4710T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403215 | |||||||
chr11:117403283 | G | A | 1 | a0006c0006t0007g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3502-4642G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403283 | |||||||
chr11:117403296 | G | A | 1 | a0001c0002t0002g0343 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3502-4629G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403296 | |||||||
chr11:117403312 | G | T | 2 | a0009c0021t0019g0085 a0019c0032t0020g0191 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3502-4613G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403312 | |||||||
chr11:117403805 | T | A | 29 | a0002c0001t0003g0069 a0002c0001t0003g0095 a0002c0001t0003g0099 others(26): Show |
29 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.3502-4120T>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117403805 | |||||||
chr11:117404022 | C | T | 1 | a0004c0004t0001g0283 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3502-3903C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404022 | |||||||
chr11:117404114 | G | C | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3502-3811G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404114 | |||||||
chr11:117404362 | G | A | 1 | a0001c0002t0002g0010 | 2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3502-3563G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404362 | |||||||
chr11:117404638 | C | T | 1 | a0003c0022t0005g0223 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3502-3287C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404638 | |||||||
chr11:117404792 | T | G | 5 | a0006c0006t0008g0048 a0009c0020t0014g0321 a0009c0021t0019g0085 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502-3133T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404792 | |||||||
chr11:117404800 | A | G | 1 | a0002c0001t0003g0137 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3502-3125A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404800 | |||||||
chr11:117404845 | G | C | 135 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0005g0349 others(132): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.3502-3080G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117404845 | |||||||
chr11:117405099 | G | A | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-2826G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405099 | |||||||
chr11:117405171 | G | C | 91 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0005g0349 others(88): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.3502-2754G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405171 | |||||||
chr11:117405795 | C | G | 1 | a0001c0005t0005g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3502-2130C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405795 | |||||||
chr11:117405985 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3502-1940T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117405985 | |||||||
chr11:117406067 | T | G | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502-1858T>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406067 | |||||||
chr11:117406086 | C | T | 61 | a0001c0005t0005g0323 a0001c0005t0005g0325 a0001c0005t0005g0349 others(58): Show |
68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.3502-1839C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406086 | |||||||
chr11:117406234 | C | T | 1 | a0004c0004t0001g0289 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3502-1691C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406234 | |||||||
chr11:117406338 | A | G | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.3502-1587A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406338 | |||||||
chr11:117406517 | A | C | 1 | a0004c0004t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3502-1408A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406517 | |||||||
chr11:117406613 | CGTACATG others(11): Show |
C | 1 | a0015c0029t0012g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3502-1311_3502-129 others(22): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406613 | |||||||
chr11:117406637 | A | C | 1 | a0001c0002t0002g0308 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3502-1288A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406637 | |||||||
chr11:117406649 | G | A | 4 | a0001c0002t0002g0002 a0001c0002t0002g0147 a0001c0002t0002g0157 others(1): Show |
7 | HG00544.hp2 HG02083.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3502-1276G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406649 | |||||||
chr11:117406869 | G | A | 1 | a0001c0005t0005g0036 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3502-1056G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406869 | |||||||
chr11:117406934 | A | G | 1 | a0001c0002t0001g0311 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3502-991A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117406934 | |||||||
chr11:117407026 | G | A | 1 | a0001c0005t0005g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3502-899G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407026 | |||||||
chr11:117407199 | G | A | 2 | a0002c0001t0003g0185 a0002c0001t0003g0186 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3502-726G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407199 | |||||||
chr11:117407220 | G | C | 2 | a0009c0020t0014g0321 a0026c0018t0014g0263 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3502-705G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407220 | |||||||
chr11:117407457 | C | CA | 125 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(122): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.3502-445dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | ||||||
chr11:117407457 | C | CAA | 21 | a0001c0002t0002g0149 a0001c0002t0002g0151 a0001c0002t0004g0165 others(18): Show |
21 | HG00408.hp1 HG00597.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3502-446_3502-445d others(4): Show |
CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | ||||||
chr11:117407457 | CA | C | 73 | a0001c0002t0001g0043 a0001c0002t0001g0074 a0001c0005t0005g0323 others(70): Show |
80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.3502-445delA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr11 | 117407457 | ||||||
chr11:117407504 | A | C | 1 | a0001c0005t0005g0268 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3502-421A>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407504 | |||||||
chr11:117407619 | C | T | 1 | a0004c0034t0007g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3502-306C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 27/32 | chr11 | 117407619 | |||||||
chr11:117408056 | C | T | 1 | a0001c0002t0004g0165 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3609+24C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408056 | |||||||
chr11:117408121 | G | T | 2 | a0002c0001t0003g0137 a0002c0001t0003g0138 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3609+89G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408121 | |||||||
chr11:117408147 | A | G | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3609+115A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408147 | |||||||
chr11:117408251 | G | GA | 6 | a0004c0009t0008g0024 a0004c0009t0008g0025 a0004c0009t0008g0026 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.3609+221dupA | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr11 | 117408251 | ||||||
chr11:117408380 | C | T | 2 | a0001c0002t0002g0022 a0001c0002t0002g0347 |
3 | NA18944.hp1 NA19007.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3609+348C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408380 | |||||||
chr11:117408849 | C | T | 1 | a0009c0021t0019g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3610-41C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 28/32 | chr11 | 117408849 | |||||||
chr11:117409279 | G | C | 1 | a0003c0022t0005g0223 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3748+251G>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 29/32 | chr11 | 117409279 | |||||||
chr11:117410008 | TC | T | 63 | a0001c0002t0001g0320 a0001c0002t0002g0002 a0001c0002t0002g0010 others(60): Show |
73 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.4096+45delC | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr11 | 117410008 | ||||||
chr11:117410046 | T | C | 2 | a0004c0034t0007g0042 a0014c0030t0021g0041 |
2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4096+81T>C | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410046 | |||||||
chr11:117410064 | C | G | 3 | a0008c0011t0012g0083 a0008c0011t0012g0084 a0015c0029t0012g0082 |
3 | HG02572.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4096+99C>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410064 | |||||||
chr11:117410277 | C | T | 1 | a0001c0005t0005g0323 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4096+312C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410277 | |||||||
chr11:117410332 | A | G | 9 | a0005c0007t0006g0032 a0005c0007t0006g0033 a0005c0007t0006g0259 others(6): Show |
9 | HG00597.hp2 HG03704.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.4096+367A>G | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410332 | |||||||
chr11:117410455 | G | A | 1 | a0001c0005t0005g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4097-373G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410455 | |||||||
chr11:117410548 | G | A | 27 | a0001c0002t0001g0053 a0001c0002t0001g0073 a0001c0002t0001g0074 others(24): Show |
31 | HG01069.hp2 HG01123.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.4097-280G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410548 | |||||||
chr11:117410601 | G | T | 1 | a0004c0004t0001g0070 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4097-227G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410601 | |||||||
chr11:117410602 | G | T | 1 | a0001c0002t0002g0334 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4097-226G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410602 | |||||||
chr11:117410641 | C | T | 4 | a0009c0020t0014g0321 a0009c0021t0019g0085 a0019c0032t0020g0191 others(1): Show |
4 | HG02559.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4097-187C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410641 | |||||||
chr11:117410759 | G | A | 2 | a0009c0020t0014g0321 a0026c0018t0014g0263 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4097-69G>A | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 30/32 | chr11 | 117410759 | |||||||
chr11:117410895 | G | T | 1 | a0004c0034t0007g0042 | 1 | HG02145.hp2 | splice_donor_variant&intron_variant | HIGH | c.4163+1G>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/32 | chr11 | 117410895 | |||||||
chr11:117411750 | C | T | 1 | a0001c0002t0002g0346 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4164-45C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 31/32 | chr11 | 117411750 | |||||||
chr11:117411999 | C | T | 1 | a0001c0002t0023g0241 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4287-73C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 32/32 | chr11 | 117411999 | |||||||
chr11:117412026 | C | T | 68 | a0001c0002t0003g0175 a0002c0001t0003g0001 a0002c0001t0003g0013 others(65): Show |
75 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.4287-46C>T | CEP164 | ENSG00000110274.16 | transcript | ENST00000278935.8 | protein_coding | 32/32 | chr11 | 117412026 |