Item | Value |
---|---|
geneid | 1497 |
ensemblid | ENSG00000040531.16 |
hgncid | 2518 |
symbol | CTNS |
name | cystinosin, lysosomal cystine transporter |
refseq_nuc | NM_004937.3 |
refseq_prot | NP_004928.2 |
ensembl_nuc | ENST00000046640.9 |
ensembl_prot | ENSP00000046640.4 |
mane_status | MANE Select |
chr | chr17 |
start | 3636760 |
end | 3663103 |
strand | + |
ver | v1.2 |
region | chr17:3636760-3663103 |
region5000 | chr17:3631760-3668103 |
regionname0 | CTNS_chr17_3636760_3663103 |
regionname5000 | CTNS_chr17_3631760_3668103 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 367 | 299 | 41 | 63 | 141 | 13 | 40 | 104 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0002 | 1/0 | 367 | 63 | 32 | 9 | 16 | 1 | 4 | 13 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0003 | 0/0 | 367 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0004 | 0/0 | 367 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0005 | 0/0 | 367 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0006 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0007 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
a0008 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | MIRNW others(362): Show |
chr17 | 3631760 | 3668103 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1101 | 230 | 27 | 48 | 111 | 8 | 35 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0001c0003 | 0/0 | 1101 | 54 | 0 | 14 | 30 | 5 | 5 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0001c0004 | 0/0 | 1101 | 14 | 14 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0001c0012 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0002c0002 | 1/0 | 1101 | 62 | 31 | 9 | 16 | 1 | 4 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0002c0008 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0003c0005 | 0/0 | 1101 | 5 | 5 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0004c0010 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0005c0009 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0006c0007 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0007c0006 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 | ||
a0008c0011 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | ATGAT others(1096): Show |
chr17 | 3631760 | 3668103 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4139 | 66 | 0 | 13 | 46 | 2 | 5 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0002 | 0/0 | 4139 | 43 | 5 | 11 | 19 | 4 | 4 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0003 | 0/0 | 4141 | 11 | 0 | 0 | 10 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0004 | 0/0 | 4138 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0005 | 0/0 | 4139 | 26 | 0 | 11 | 7 | 0 | 8 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0006 | 0/0 | 4142 | 6 | 0 | 0 | 4 | 0 | 2 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0007 | 0/0 | 4139 | 9 | 3 | 0 | 0 | 0 | 6 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0012 | 0/0 | 4139 | 5 | 0 | 3 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0013 | 0/0 | 4143 | 3 | 0 | 3 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0015 | 0/0 | 4139 | 4 | 3 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0020 | 0/0 | 4138 | 3 | 1 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0021 | 0/0 | 4144 | 2 | 1 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4139): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0022 | 0/0 | 4143 | 2 | 0 | 1 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0028 | 0/0 | 4139 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0029 | 0/0 | 4139 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0030 | 0/0 | 4138 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0031 | 0/0 | 4139 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0032 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0035 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0037 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0039 | 0/0 | 4145 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4140): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0040 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4139): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0041 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0042 | 0/0 | 4144 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4139): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0043 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0044 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0045 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0048 | 0/0 | 4143 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0049 | 0/0 | 4141 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0051 | 0/0 | 4141 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0052 | 0/0 | 4141 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0059 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0060 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4135): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0064 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0065 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0066 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0067 | 0/0 | 4138 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0068 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0073 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0074 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0075 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0076 | 0/1 | 4139 | 1 | 0 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0077 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0078 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0079 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0080 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0081 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0082 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0083 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0084 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0085 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0086 | 0/0 | 4137 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4132): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0087 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0088 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0089 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0090 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0001t0091 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0001 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0003 | 0/0 | 4141 | 19 | 0 | 1 | 14 | 2 | 2 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0006 | 0/0 | 4142 | 11 | 0 | 2 | 7 | 0 | 2 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0009 | 0/0 | 4141 | 6 | 0 | 5 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0016 | 0/0 | 4139 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0017 | 0/0 | 4141 | 3 | 0 | 1 | 0 | 2 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0023 | 0/0 | 4142 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0024 | 0/0 | 4141 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0033 | 0/0 | 4141 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0036 | 0/0 | 4141 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0038 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0046 | 0/0 | 4142 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0047 | 0/0 | 4142 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4137): Show |
chr17 | 3631760 | 3668103 |
a0001c0003t0050 | 0/0 | 4140 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4135): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0005 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0008 | 0/0 | 4139 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0018 | 0/0 | 4139 | 3 | 3 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0025 | 0/0 | 4139 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0026 | 0/0 | 4139 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0054 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0055 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0056 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0004t0057 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0001c0012t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0004 | 0/0 | 4138 | 28 | 22 | 4 | 0 | 0 | 2 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0007 | 0/0 | 4139 | 4 | 0 | 4 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0010 | 0/0 | 4138 | 6 | 5 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0011 | 0/0 | 4139 | 5 | 0 | 0 | 5 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0014 | 0/0 | 4139 | 4 | 0 | 0 | 3 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0019 | 0/0 | 4139 | 3 | 0 | 0 | 2 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0027 | 0/0 | 4139 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0032 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0034 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0053 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0058 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0061 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0062 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0063 | 0/0 | 4140 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4135): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0069 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4131): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0070 | 0/0 | 4138 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4133): Show |
chr17 | 3631760 | 3668103 |
a0002c0002t0072 | 1/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0002c0008t0071 | 0/0 | 4139 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0003c0005t0008 | 0/0 | 4139 | 5 | 5 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0004c0010t0001 | 0/0 | 4139 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0005c0009t0013 | 0/0 | 4143 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4138): Show |
chr17 | 3631760 | 3668103 |
a0006c0007t0005 | 0/0 | 4139 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
a0007c0006t0003 | 0/0 | 4141 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4136): Show |
chr17 | 3631760 | 3668103 |
a0008c0011t0002 | 0/0 | 4139 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | GCATT others(4134): Show |
chr17 | 3631760 | 3668103 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0002 | 0/0 | 10 | 4 | 5 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0006g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0012g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0013g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0013g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0013g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0015g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0020g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0020g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0020g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0021g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0021g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0022g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0028g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0029g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0029g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0030g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0031g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0031g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0032g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0035g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0037g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0039g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0040g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0041g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0042g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0043g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0044g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0045g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0048g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0049g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0051g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0052g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0059g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0060g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0064g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0065g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0066g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0067g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0068g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0073g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0074g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0075g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0076g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0077g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0078g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0079g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0080g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0081g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0082g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0083g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0084g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0085g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0086g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0087g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0088g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0089g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0090g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0001t0091g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0006g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0009g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0009g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0016g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0016g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0016g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0017g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0017g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0017g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0023g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0023g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0024g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0033g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0033g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0036g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0038g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0046g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0047g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0003t0050g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0008g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0018g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0025g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0025g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0026g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0026g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0054g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0055g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0056g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0004t0057g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0001c0012t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0001 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0007g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0010g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0010g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0011g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0011g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0011g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0014g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0014g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0014g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0014g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0019g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0019g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0019g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0027g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0027g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0032g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0034g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0053g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0058g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0061g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0062g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0063g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0069g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0070g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0002t0072g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0002c0008t0071g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0003c0005t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0003c0005t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0003c0005t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0003c0005t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0003c0005t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0004c0010t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0005c0009t0013g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0006c0007t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0007c0006t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
a0008c0011t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00099 | hp2 | a0001 | c0003 | t0003 | g0230 | EUR | GBR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | FIN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00323 | hp2 | a0002 | c0002 | t0010 | g0225 | EUR | FIN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00408 | hp1 | a0001 | c0003 | t0006 | g0186 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00408 | hp2 | a0002 | c0002 | t0069 | g0036 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00423 | hp1 | a0001 | c0003 | t0003 | g0220 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00597 | hp1 | a0001 | c0003 | t0003 | g0030 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00621 | hp2 | a0002 | c0002 | t0014 | g0244 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0228 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00642 | hp1 | a0002 | c0002 | t0007 | g0036 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00642 | hp2 | a0001 | c0003 | t0023 | g0033 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00673 | hp2 | a0001 | c0003 | t0006 | g0030 | EAS | CHS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00733 | hp1 | a0002 | c0002 | t0062 | g0242 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00733 | hp2 | a0001 | c0001 | t0066 | g0103 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00735 | hp1 | a0004 | c0010 | t0001 | g0124 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00738 | hp1 | a0005 | c0009 | t0013 | g0015 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01069 | hp1 | a0001 | c0003 | t0024 | g0003 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0113 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01071 | hp1 | a0001 | c0001 | t0013 | g0112 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01071 | hp2 | a0001 | c0003 | t0024 | g0003 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01074 | hp2 | a0001 | c0003 | t0017 | g0203 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01099 | hp2 | a0001 | c0001 | t0035 | g0136 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01109 | hp2 | a0002 | c0002 | t0004 | g0235 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01167 | hp2 | a0002 | c0002 | t0004 | g0236 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01168 | hp1 | a0002 | c0002 | t0007 | g0241 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01175 | hp2 | a0001 | c0003 | t0046 | g0003 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01192 | hp1 | a0001 | c0003 | t0009 | g0033 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01192 | hp2 | a0001 | c0001 | t0022 | g0212 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01243 | hp2 | a0002 | c0002 | t0004 | g0239 | AMR | PUR | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01255 | hp1 | a0001 | c0003 | t0009 | g0218 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0015 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01258 | hp1 | a0001 | c0001 | t0077 | g0074 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01258 | hp2 | a0002 | c0002 | t0007 | g0035 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01346 | hp1 | a0001 | c0003 | t0006 | g0003 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01346 | hp2 | a0001 | c0003 | t0009 | g0003 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01358 | hp2 | a0001 | c0012 | t0001 | g0146 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01361 | hp1 | a0001 | c0001 | t0012 | g0009 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01361 | hp2 | a0001 | c0003 | t0009 | g0188 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01433 | hp1 | a0002 | c0002 | t0007 | g0035 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01433 | hp2 | a0001 | c0001 | t0075 | g0174 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0089 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0181 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01515 | hp2 | a0001 | c0003 | t0017 | g0231 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01517 | hp1 | a0001 | c0003 | t0017 | g0208 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01884 | hp2 | a0001 | c0004 | t0054 | g0105 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01891 | hp1 | a0001 | c0001 | t0028 | g0029 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01891 | hp2 | a0002 | c0002 | t0010 | g0001 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01928 | hp2 | a0001 | c0001 | t0083 | g0148 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01934 | hp1 | a0001 | c0003 | t0003 | g0222 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0081 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01943 | hp2 | a0001 | c0001 | t0012 | g0009 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0057 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01981 | hp2 | a0001 | c0003 | t0023 | g0207 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02004 | hp2 | a0001 | c0001 | t0081 | g0130 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02015 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02055 | hp1 | a0001 | c0004 | t0025 | g0039 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02055 | hp2 | a0001 | c0004 | t0056 | g0107 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0084 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02080 | hp2 | a0001 | c0001 | t0082 | g0179 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02083 | hp2 | a0001 | c0001 | t0051 | g0003 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02132 | hp1 | a0001 | c0001 | t0091 | g0006 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02132 | hp2 | a0001 | c0001 | t0085 | g0170 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02135 | hp1 | a0002 | c0002 | t0011 | g0243 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02148 | hp1 | a0001 | c0003 | t0009 | g0205 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02155 | hp1 | a0001 | c0003 | t0050 | g0209 | EAS | CDX | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02155 | hp2 | a0001 | c0001 | t0030 | g0082 | EAS | CDX | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02257 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02257 | hp2 | a0001 | c0004 | t0018 | g0016 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02258 | hp1 | a0001 | c0004 | t0018 | g0016 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02258 | hp2 | a0001 | c0001 | t0041 | g0079 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02273 | hp2 | a0001 | c0001 | t0012 | g0009 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02300 | hp1 | a0001 | c0003 | t0006 | g0003 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02451 | hp1 | a0001 | c0004 | t0055 | g0039 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0037 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02523 | hp1 | a0001 | c0003 | t0036 | g0217 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02572 | hp1 | a0002 | c0002 | t0004 | g0237 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02572 | hp2 | a0002 | c0002 | t0061 | g0248 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02602 | hp1 | a0001 | c0001 | t0021 | g0058 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02615 | hp1 | a0003 | c0005 | t0008 | g0046 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02622 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02622 | hp2 | a0002 | c0002 | t0004 | g0041 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02630 | hp1 | a0001 | c0001 | t0021 | g0061 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02647 | hp1 | a0001 | c0004 | t0026 | g0263 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02647 | hp2 | a0002 | c0002 | t0004 | g0041 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02683 | hp1 | a0002 | c0002 | t0004 | g0034 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0116 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02698 | hp1 | a0002 | c0002 | t0019 | g0247 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02698 | hp2 | a0001 | c0001 | t0065 | g0163 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02717 | hp1 | a0001 | c0001 | t0048 | g0059 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02717 | hp2 | a0002 | c0002 | t0010 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02735 | hp1 | a0001 | c0001 | t0080 | g0156 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0101 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02818 | hp1 | a0002 | c0002 | t0004 | g0238 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02818 | hp2 | a0002 | c0002 | t0010 | g0229 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02886 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0096 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02895 | hp2 | a0002 | c0002 | t0010 | g0180 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02896 | hp1 | a0002 | c0002 | t0063 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0226 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02922 | hp1 | a0002 | c0002 | t0004 | g0233 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02922 | hp2 | a0003 | c0005 | t0008 | g0266 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02970 | hp1 | a0001 | c0004 | t0008 | g0040 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02970 | hp2 | a0001 | c0004 | t0026 | g0262 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02976 | hp2 | a0001 | c0004 | t0018 | g0016 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0071 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0073 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03041 | hp1 | a0001 | c0001 | t0028 | g0029 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0001 | AFR | GWD | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03098 | hp1 | a0002 | c0008 | t0071 | g0261 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0109 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03130 | hp1 | a0003 | c0005 | t0008 | g0048 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03130 | hp2 | a0002 | c0002 | t0004 | g0240 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03139 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03139 | hp2 | a0001 | c0001 | t0044 | g0251 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03209 | hp2 | a0001 | c0001 | t0040 | g0077 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03239 | hp1 | a0002 | c0002 | t0004 | g0034 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03486 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03486 | hp2 | a0001 | c0004 | t0008 | g0040 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03491 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0086 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03492 | hp2 | a0001 | c0001 | t0084 | g0142 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03516 | hp1 | a0001 | c0001 | t0043 | g0093 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03516 | hp2 | a0001 | c0001 | t0059 | g0014 | AFR | ESN | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03579 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03579 | hp2 | a0003 | c0005 | t0008 | g0049 | AFR | MSL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03654 | hp1 | a0001 | c0001 | t0039 | g0102 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03654 | hp2 | a0001 | c0001 | t0073 | g0175 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03669 | hp1 | a0001 | c0003 | t0047 | g0219 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0173 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0117 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0067 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03831 | hp1 | a0002 | c0002 | t0014 | g0254 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03831 | hp2 | a0001 | c0003 | t0006 | g0232 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0055 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03927 | hp1 | a0001 | c0001 | t0068 | g0097 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0126 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03942 | hp1 | a0001 | c0001 | t0074 | g0028 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG03942 | hp2 | a0001 | c0003 | t0006 | g0200 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0210 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0211 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0098 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04184 | hp2 | a0001 | c0003 | t0003 | g0221 | SAS | BEB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04204 | hp1 | a0001 | c0001 | t0015 | g0028 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04204 | hp2 | a0006 | c0007 | t0005 | g0054 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04228 | hp1 | a0007 | c0006 | t0003 | g0202 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG04228 | hp2 | a0001 | c0001 | t0064 | g0090 | SAS | STU | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18747 | hp1 | a0001 | c0003 | t0016 | g0187 | EAS | CHB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18747 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | CHB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18906 | hp1 | a0001 | c0004 | t0057 | g0264 | AFR | YRI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18906 | hp2 | a0001 | c0001 | t0045 | g0249 | AFR | YRI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18943 | hp1 | a0001 | c0003 | t0006 | g0196 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18944 | hp2 | a0002 | c0002 | t0019 | g0256 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18945 | hp1 | a0001 | c0003 | t0033 | g0017 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18945 | hp2 | a0001 | c0001 | t0031 | g0026 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18948 | hp1 | a0001 | c0001 | t0049 | g0198 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18948 | hp2 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18949 | hp1 | a0002 | c0002 | t0027 | g0223 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18950 | hp1 | a0001 | c0001 | t0020 | g0120 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18956 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18957 | hp2 | a0001 | c0001 | t0067 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18959 | hp2 | a0002 | c0002 | t0011 | g0258 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18961 | hp1 | a0001 | c0003 | t0006 | g0214 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0032 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18967 | hp2 | a0001 | c0001 | t0090 | g0106 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18968 | hp1 | a0002 | c0002 | t0011 | g0253 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18968 | hp2 | a0001 | c0001 | t0079 | g0008 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18969 | hp2 | a0001 | c0001 | t0032 | g0135 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18970 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18970 | hp2 | a0001 | c0001 | t0087 | g0140 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18974 | hp1 | a0001 | c0001 | t0029 | g0018 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18975 | hp1 | a0001 | c0001 | t0022 | g0194 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18977 | hp1 | a0001 | c0003 | t0003 | g0032 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18979 | hp1 | a0002 | c0002 | t0027 | g0224 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18979 | hp2 | a0001 | c0003 | t0038 | g0215 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18980 | hp1 | a0002 | c0002 | t0058 | g0246 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18982 | hp2 | a0001 | c0001 | t0088 | g0151 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18984 | hp2 | a0001 | c0001 | t0030 | g0091 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18988 | hp1 | a0008 | c0011 | t0002 | g0013 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18992 | hp2 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18994 | hp1 | a0001 | c0003 | t0006 | g0206 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18997 | hp2 | a0001 | c0001 | t0089 | g0204 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA18999 | hp2 | a0001 | c0003 | t0016 | g0185 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19002 | hp1 | a0002 | c0002 | t0014 | g0245 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19009 | hp2 | a0001 | c0001 | t0031 | g0168 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19011 | hp1 | a0001 | c0003 | t0033 | g0190 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19012 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19012 | hp2 | a0001 | c0001 | t0078 | g0008 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19030 | hp2 | a0001 | c0004 | t0005 | g0075 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19043 | hp1 | a0001 | c0001 | t0037 | g0108 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19043 | hp2 | a0001 | c0001 | t0052 | g0060 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19062 | hp1 | a0002 | c0002 | t0034 | g0038 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19062 | hp2 | a0001 | c0001 | t0020 | g0177 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19064 | hp2 | a0001 | c0003 | t0016 | g0184 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19065 | hp1 | a0001 | c0001 | t0029 | g0099 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19066 | hp1 | a0001 | c0003 | t0006 | g0011 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19068 | hp1 | a0002 | c0002 | t0011 | g0038 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19068 | hp2 | a0002 | c0002 | t0014 | g0259 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19084 | hp1 | a0001 | c0003 | t0006 | g0213 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19084 | hp2 | a0002 | c0002 | t0019 | g0252 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19085 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19087 | hp1 | a0002 | c0002 | t0032 | g0255 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19087 | hp2 | a0001 | c0001 | t0086 | g0121 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19089 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19091 | hp2 | a0002 | c0002 | t0011 | g0260 | EAS | JPT | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19240 | hp1 | a0002 | c0002 | t0070 | g0234 | AFR | YRI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA19240 | hp2 | a0001 | c0001 | t0060 | g0052 | AFR | YRI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20752 | hp1 | a0001 | c0001 | t0042 | g0015 | EUR | TSI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20752 | hp2 | a0001 | c0003 | t0009 | g0003 | EUR | TSI | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | GIH | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0037 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0001 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02486 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02559 | hp1 | a0002 | c0002 | t0053 | g0250 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
HG02559 | hp2 | a0003 | c0005 | t0008 | g0047 | AFR | ACB | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | USA | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA20300 | hp2 | a0001 | c0004 | t0025 | g0265 | AFR | USA | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0172 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
NA21309 | hp2 | a0001 | c0001 | t0020 | g0227 | AFR | LWK | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
homoSapiens | chm13v2 | a0001 | c0001 | t0076 | g0042 | REF | REF | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
homoSapiens | grch38p0 | a0002 | c0002 | t0072 | g0257 | REF | REF | CTNS_chr17_3631760_3668103 | CTNS | chr17 | 3631760 | 3668103 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:3640253 | T | C | 1 | a0007 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.47T>C | p.Leu16Pro | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/12 | 348/4139 | 47/1104 | 16/367 | chr17 | 3640253 | |||
chr17:3647506 | G | A | 1 | a0003 | 5 | HG02559.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.124G>A | p.Val42Ile | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/12 | 425/4139 | 124/1104 | 42/367 | chr17 | 3647506 | |||
chr17:3655068 | T | G | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.296T>G | p.Val99Gly | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 6/12 | 597/4139 | 296/1104 | 99/367 | chr17 | 3655068 | |||
chr17:3656512 | G | A | 1 | a0005 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.487G>A | p.Val163Met | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 8/12 | 788/4139 | 487/1104 | 163/367 | chr17 | 3656512 | |||
chr17:3658102 | C | T | 7 | a0001 a0003 a0004 others(4): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
missense_variant | MODERATE | c.779C>T | p.Thr260Ile | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/12 | 1080/4139 | 779/1104 | 260/367 | chr17 | 3658102 | |||
chr17:3659943 | T | A | 1 | a0004 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.938T>A | p.Leu313His | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/12 | 1239/4139 | 938/1104 | 313/367 | chr17 | 3659943 | |||
chr17:3660256 | G | A | 1 | a0008 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.991G>A | p.Gly331Arg | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1292/4139 | 991/1104 | 331/367 | chr17 | 3660256 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:3656487 | T | C | 3 | a0001c0004 a0002c0008 a0003c0005 |
20 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
splice_region_variant&synonymous_variant | LOW | c.462T>C | p.Ser154Ser | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 8/12 | 763/4139 | 462/1104 | 154/367 | chr17 | 3656487 | |||
chr17:3656529 | G | A | 2 | a0001c0003 a0007c0006 |
55 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
synonymous_variant | LOW | c.504G>A | p.Thr168Thr | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 8/12 | 805/4139 | 504/1104 | 168/367 | chr17 | 3656529 | |||
chr17:3656726 | C | T | 1 | a0001c0012 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.612C>T | p.Asn204Asn | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/12 | 913/4139 | 612/1104 | 204/367 | chr17 | 3656726 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:3636796 | C | T | 1 | a0001c0003t0033 | 2 | NA18945.hp1 NA19011.hp1 |
5_prime_UTR_variant | MODIFIER | c.-265C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 1/12 | 3411 | chr17 | 3636796 | ||||||
chr17:3637258 | A | G | 1 | a0001c0001t0091 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/12 | 2949 | chr17 | 3637258 | ||||||
chr17:3660392 | A | C | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 23 | chr17 | 3660392 | ||||||
chr17:3660442 | G | T | 1 | a0001c0001t0089 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 73 | chr17 | 3660442 | ||||||
chr17:3660449 | G | A | 1 | a0002c0002t0034 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*80G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 80 | chr17 | 3660449 | ||||||
chr17:3660631 | G | A | 1 | a0001c0001t0035 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 262 | chr17 | 3660631 | ||||||
chr17:3660669 | C | G | 22 | a0001c0001t0001 a0001c0001t0020 a0001c0001t0031 others(19): Show |
90 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*300C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 300 | chr17 | 3660669 | ||||||
chr17:3660773 | C | T | 1 | a0001c0001t0075 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 404 | chr17 | 3660773 | ||||||
chr17:3660774 | G | A | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*405G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 405 | chr17 | 3660774 | ||||||
chr17:3660779 | A | G | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*410A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 410 | chr17 | 3660779 | ||||||
chr17:3660790 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*421T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 421 | chr17 | 3660790 | ||||||
chr17:3660874 | C | A | 1 | a0002c0002t0053 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 505 | chr17 | 3660874 | ||||||
chr17:3660896 | G | A | 9 | a0001c0004t0008 a0001c0004t0018 a0001c0004t0025 others(6): Show |
18 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*527G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 527 | chr17 | 3660896 | ||||||
chr17:3660924 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*555T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 555 | chr17 | 3660924 | ||||||
chr17:3660941 | A | G | 34 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(31): Show |
93 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*572A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 572 | chr17 | 3660941 | ||||||
chr17:3660996 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*627T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 627 | chr17 | 3660996 | ||||||
chr17:3661000 | T | C | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*631T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 631 | chr17 | 3661000 | ||||||
chr17:3661084 | C | T | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 715 | chr17 | 3661084 | ||||||
chr17:3661106 | T | A | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(28): Show |
105 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 737 | chr17 | 3661106 | ||||||
chr17:3661107 | T | G | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*738T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 738 | chr17 | 3661107 | ||||||
chr17:3661151 | G | A | 1 | a0001c0001t0077 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*782G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 782 | chr17 | 3661151 | ||||||
chr17:3661151 | G | C | 1 | a0001c0003t0036 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*782G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 782 | chr17 | 3661151 | ||||||
chr17:3661204 | A | C | 1 | a0002c0002t0070 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 835 | chr17 | 3661204 | ||||||
chr17:3661208 | C | A | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 839 | chr17 | 3661208 | ||||||
chr17:3661209 | T | C | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 840 | chr17 | 3661209 | ||||||
chr17:3661210 | G | A | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 841 | chr17 | 3661210 | ||||||
chr17:3661212 | C | T | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*843C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 843 | chr17 | 3661212 | ||||||
chr17:3661214 | A | G | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 845 | chr17 | 3661214 | ||||||
chr17:3661216 | C | T | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*847C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 847 | chr17 | 3661216 | ||||||
chr17:3661217 | G | C | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 848 | chr17 | 3661217 | ||||||
chr17:3661220 | G | A | 3 | a0001c0001t0037 a0001c0004t0018 a0001c0004t0054 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*851G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 851 | chr17 | 3661220 | ||||||
chr17:3661221 | A | T | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 852 | chr17 | 3661221 | ||||||
chr17:3661222 | C | G | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 853 | chr17 | 3661222 | ||||||
chr17:3661223 | C | T | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 854 | chr17 | 3661223 | ||||||
chr17:3661224 | A | T | 1 | a0001c0001t0090 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 855 | chr17 | 3661224 | ||||||
chr17:3661311 | C | A | 1 | a0001c0003t0038 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 942 | chr17 | 3661311 | ||||||
chr17:3661393 | C | T | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(28): Show |
88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1024C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1024 | chr17 | 3661393 | ||||||
chr17:3661394 | A | G | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1025A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1025 | chr17 | 3661394 | ||||||
chr17:3661399 | T | TGTC | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(28): Show |
88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1033dupGTC | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1034 | INFO_REALIGN_3_PRIME | chr17 | 3661399 | |||||
chr17:3661417 | A | AG | 11 | a0001c0001t0003 a0001c0001t0049 a0001c0001t0051 others(8): Show |
48 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1052dupG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1053 | INFO_REALIGN_3_PRIME | chr17 | 3661417 | |||||
chr17:3661417 | A | AGG | 12 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0022 others(9): Show |
31 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1052dupGG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1053 | INFO_REALIGN_3_PRIME | chr17 | 3661417 | |||||
chr17:3661417 | A | AGGG | 6 | a0001c0001t0021 a0001c0001t0039 a0001c0001t0040 others(3): Show |
7 | HG02258.hp2 HG02602.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1050_*1052dupGGG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1053 | INFO_REALIGN_3_PRIME | chr17 | 3661417 | |||||
chr17:3661422 | T | G | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(28): Show |
88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1053T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1053 | chr17 | 3661422 | ||||||
chr17:3661455 | G | A | 1 | a0001c0001t0073 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1086 | chr17 | 3661455 | ||||||
chr17:3661485 | C | T | 30 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(27): Show |
87 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1116C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1116 | chr17 | 3661485 | ||||||
chr17:3661486 | G | A | 6 | a0002c0002t0011 a0002c0002t0014 a0002c0002t0019 others(3): Show |
16 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1117G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1117 | chr17 | 3661486 | ||||||
chr17:3661497 | G | A | 2 | a0001c0004t0025 a0001c0004t0055 |
3 | HG02055.hp1 HG02451.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1128G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1128 | chr17 | 3661497 | ||||||
chr17:3661521 | A | G | 29 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(26): Show |
86 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1152A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1152 | chr17 | 3661521 | ||||||
chr17:3661528 | C | T | 1 | a0001c0001t0087 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1159C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1159 | chr17 | 3661528 | ||||||
chr17:3661534 | C | T | 6 | a0002c0002t0011 a0002c0002t0014 a0002c0002t0019 others(3): Show |
16 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1165C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1165 | chr17 | 3661534 | ||||||
chr17:3661542 | ACT | A | 32 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(29): Show |
89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177delCT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1176 | INFO_REALIGN_3_PRIME | chr17 | 3661542 | |||||
chr17:3661575 | T | C | 2 | a0001c0001t0059 a0001c0004t0018 |
4 | HG02257.hp2 HG02258.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1206T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1206 | chr17 | 3661575 | ||||||
chr17:3661594 | C | T | 1 | a0001c0001t0085 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1225 | chr17 | 3661594 | ||||||
chr17:3661705 | G | A | 1 | a0001c0001t0078 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1336G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1336 | chr17 | 3661705 | ||||||
chr17:3661809 | A | G | 76 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(73): Show |
277 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1440A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1440 | chr17 | 3661809 | ||||||
chr17:3661885 | C | G | 1 | a0001c0001t0089 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1516C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1516 | chr17 | 3661885 | ||||||
chr17:3661886 | G | C | 1 | a0001c0001t0089 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1517 | chr17 | 3661886 | ||||||
chr17:3661908 | T | A | 1 | a0001c0001t0089 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1539 | chr17 | 3661908 | ||||||
chr17:3661947 | C | G | 6 | a0001c0001t0021 a0001c0001t0037 a0001c0001t0043 others(3): Show |
7 | HG02602.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1578 | chr17 | 3661947 | ||||||
chr17:3661964 | C | T | 11 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0037 others(8): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1595C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1595 | chr17 | 3661964 | ||||||
chr17:3662002 | C | G | 11 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0037 others(8): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1633C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1633 | chr17 | 3662002 | ||||||
chr17:3662034 | A | G | 12 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0037 others(9): Show |
15 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1665A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1665 | chr17 | 3662034 | ||||||
chr17:3662120 | A | G | 1 | a0001c0001t0051 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1751 | chr17 | 3662120 | ||||||
chr17:3662180 | G | A | 1 | a0001c0001t0043 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1811G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1811 | chr17 | 3662180 | ||||||
chr17:3662235 | C | T | 11 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0037 others(8): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1866C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1866 | chr17 | 3662235 | ||||||
chr17:3662265 | C | G | 1 | a0001c0001t0068 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1896 | chr17 | 3662265 | ||||||
chr17:3662266 | A | T | 1 | a0001c0001t0089 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1897A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1897 | chr17 | 3662266 | ||||||
chr17:3662268 | G | A | 1 | a0001c0001t0044 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1899G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1899 | chr17 | 3662268 | ||||||
chr17:3662311 | C | CA | 12 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0022 others(9): Show |
16 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1957dupA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1958 | INFO_REALIGN_3_PRIME | chr17 | 3662311 | |||||
chr17:3662311 | CA | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(47): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1957delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1957 | INFO_REALIGN_3_PRIME | chr17 | 3662311 | |||||
chr17:3662311 | CAA | C | 8 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0030 others(5): Show |
44 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1956_*1957delAA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 1956 | INFO_REALIGN_3_PRIME | chr17 | 3662311 | |||||
chr17:3662381 | C | T | 1 | a0001c0004t0054 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2012 | chr17 | 3662381 | ||||||
chr17:3662452 | G | A | 1 | a0001c0001t0086 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2083G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2083 | chr17 | 3662452 | ||||||
chr17:3662484 | G | A | 10 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0040 others(7): Show |
13 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2115G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2115 | chr17 | 3662484 | ||||||
chr17:3662488 | G | T | 1 | a0001c0001t0037 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2119 | chr17 | 3662488 | ||||||
chr17:3662501 | G | A | 1 | a0001c0001t0037 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2132 | chr17 | 3662501 | ||||||
chr17:3662514 | G | A | 1 | a0001c0001t0064 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2145 | chr17 | 3662514 | ||||||
chr17:3662675 | T | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(57): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2306T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2306 | chr17 | 3662675 | ||||||
chr17:3662713 | C | T | 1 | a0001c0001t0082 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2344C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2344 | chr17 | 3662713 | ||||||
chr17:3662751 | T | TC | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*2383dupC | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2384 | INFO_REALIGN_3_PRIME | chr17 | 3662751 | |||||
chr17:3662772 | T | G | 1 | a0001c0003t0046 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2403 | chr17 | 3662772 | ||||||
chr17:3662915 | G | C | 27 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0022 others(24): Show |
80 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2546G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2546 | chr17 | 3662915 | ||||||
chr17:3662919 | G | A | 27 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0022 others(24): Show |
80 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2550G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2550 | chr17 | 3662919 | ||||||
chr17:3662938 | C | T | 40 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(37): Show |
134 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2569C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2569 | chr17 | 3662938 | ||||||
chr17:3663031 | G | A | 1 | a0001c0001t0065 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2662 | chr17 | 3663031 | ||||||
chr17:3663053 | A | G | 1 | a0001c0001t0081 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2684A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 12/12 | 2684 | chr17 | 3663053 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:3636842 | A | G | 9 | a0001c0004t0008g0040 a0001c0004t0025g0039 a0001c0004t0025g0265 others(6): Show |
11 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-230+11A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 1/11 | chr17 | 3636842 | |||||||
chr17:3636869 | A | G | 9 | a0001c0004t0008g0040 a0001c0004t0025g0039 a0001c0004t0025g0265 others(6): Show |
11 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-230+38A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 1/11 | chr17 | 3636869 | |||||||
chr17:3637021 | G | A | 2 | a0001c0004t0026g0262 a0001c0004t0026g0263 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-229-86G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 1/11 | chr17 | 3637021 | |||||||
chr17:3637399 | G | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-20+83G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637399 | |||||||
chr17:3637461 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
100 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.-20+145G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637461 | |||||||
chr17:3637465 | A | AT | 12 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0013g0015 others(9): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+165dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3637465 | ||||||
chr17:3637465 | AT | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(107): Show |
144 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.-20+165delT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3637465 | ||||||
chr17:3637465 | ATT | A | 72 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0003g0007 others(69): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-20+164_-20+165del others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3637465 | ||||||
chr17:3637623 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-20+307T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637623 | |||||||
chr17:3637812 | TCTC | T | 16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20+500_-20+502del others(3): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3637812 | ||||||
chr17:3637819 | A | G | 2 | a0001c0004t0018g0016 a0001c0004t0054g0105 |
4 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+503A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637819 | |||||||
chr17:3637848 | CCTT | C | 6 | a0001c0004t0025g0039 a0001c0004t0025g0265 a0001c0004t0026g0262 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+533_-20+535del others(3): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637848 | |||||||
chr17:3637877 | TA | T | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-20+563delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3637877 | ||||||
chr17:3637914 | C | A | 16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20+598C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637914 | |||||||
chr17:3637989 | C | A | 2 | a0001c0001t0007g0116 a0001c0001t0007g0117 |
2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-20+673C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3637989 | |||||||
chr17:3638056 | G | A | 4 | a0003c0005t0008g0046 a0003c0005t0008g0047 a0003c0005t0008g0048 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+740G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638056 | |||||||
chr17:3638137 | G | T | 4 | a0001c0001t0002g0009 a0001c0001t0012g0009 a0001c0001t0012g0104 others(1): Show |
6 | HG00733.hp2 HG01361.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+821G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638137 | |||||||
chr17:3638226 | G | GT | 9 | a0001c0003t0003g0181 a0001c0003t0003g0220 a0001c0003t0003g0221 others(6): Show |
9 | HG00099.hp2 HG00423.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+920dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3638226 | ||||||
chr17:3638226 | G | T | 2 | a0002c0002t0027g0223 a0002c0002t0027g0224 |
2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-20+910G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638226 | |||||||
chr17:3638226 | GTTTTTTT others(6): Show |
G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(95): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-20+921_-20+933del others(13): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3638226 | ||||||
chr17:3638226 | GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0002g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-20+920_-20+933del others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3638226 | ||||||
chr17:3638236 | T | G | 15 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(12): Show |
15 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+920T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638236 | |||||||
chr17:3638237 | G | T | 63 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(60): Show |
74 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-20+921G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638237 | |||||||
chr17:3638240 | T | G | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-20+924T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638240 | |||||||
chr17:3638472 | A | G | 64 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(61): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-20+1156A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638472 | |||||||
chr17:3638511 | TACAC | T | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-20+1200_-20+1203d others(6): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3638511 | ||||||
chr17:3638524 | C | T | 1 | a0001c0003t0009g0218 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-20+1208C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638524 | |||||||
chr17:3638564 | T | C | 1 | a0001c0001t0007g0051 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-20+1248T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638564 | |||||||
chr17:3638646 | C | T | 2 | a0001c0004t0018g0016 a0001c0004t0054g0105 |
4 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1330C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638646 | |||||||
chr17:3638773 | G | T | 1 | a0002c0002t0004g0240 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19-1415G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638773 | |||||||
chr17:3638781 | G | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-1407G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638781 | |||||||
chr17:3638825 | A | G | 1 | a0002c0008t0071g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-19-1363A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638825 | |||||||
chr17:3638842 | A | C | 70 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(67): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-19-1346A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638842 | |||||||
chr17:3638872 | C | T | 6 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(3): Show |
6 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-1316C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638872 | |||||||
chr17:3638914 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19-1274G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638914 | |||||||
chr17:3638989 | G | C | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19-1199G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3638989 | |||||||
chr17:3639110 | T | G | 1 | a0001c0001t0002g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-19-1078T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639110 | |||||||
chr17:3639121 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-19-1067A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639121 | |||||||
chr17:3639161 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-1027T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639161 | |||||||
chr17:3639185 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(95): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-19-1003G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639185 | |||||||
chr17:3639191 | C | T | 29 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(26): Show |
46 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-997C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639191 | |||||||
chr17:3639230 | C | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-958C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639230 | |||||||
chr17:3639280 | T | C | 1 | a0001c0001t0060g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19-908T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639280 | |||||||
chr17:3639299 | C | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-889C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639299 | |||||||
chr17:3639415 | C | A | 6 | a0001c0004t0025g0039 a0001c0004t0025g0265 a0001c0004t0026g0262 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-773C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639415 | |||||||
chr17:3639474 | G | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-714G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639474 | |||||||
chr17:3639622 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-19-566C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639622 | |||||||
chr17:3639667 | C | CAA | 96 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(93): Show |
119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-19-509_-19-508dup others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3639667 | ||||||
chr17:3639667 | CA | C | 14 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(11): Show |
28 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19-508delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3639667 | ||||||
chr17:3639696 | TA | T | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19-483delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 3639696 | ||||||
chr17:3639754 | C | T | 1 | a0001c0001t0005g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19-434C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639754 | |||||||
chr17:3639758 | T | A | 1 | a0001c0001t0002g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-19-430T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639758 | |||||||
chr17:3639902 | A | G | 1 | a0001c0003t0036g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-19-286A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639902 | |||||||
chr17:3639910 | C | T | 1 | a0001c0001t0020g0177 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-19-278C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639910 | |||||||
chr17:3639941 | T | G | 1 | a0001c0001t0082g0179 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-19-247T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639941 | |||||||
chr17:3639977 | A | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-211A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 2/11 | chr17 | 3639977 | |||||||
chr17:3640416 | G | A | 1 | a0001c0001t0005g0053 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.61+149G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640416 | |||||||
chr17:3640561 | C | G | 1 | a0002c0002t0014g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.61+294C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640561 | |||||||
chr17:3640723 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(81): Show |
101 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.61+456C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640723 | |||||||
chr17:3640727 | A | C | 1 | a0001c0001t0002g0050 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.61+460A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640727 | |||||||
chr17:3640760 | C | T | 6 | a0001c0004t0025g0039 a0001c0004t0025g0265 a0001c0004t0026g0262 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+493C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640760 | |||||||
chr17:3640854 | T | C | 2 | a0001c0001t0005g0055 a0006c0007t0005g0054 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.61+587T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640854 | |||||||
chr17:3640861 | A | C | 1 | a0001c0001t0005g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.61+594A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640861 | |||||||
chr17:3640897 | C | A | 7 | a0001c0003t0003g0030 a0001c0003t0003g0183 a0001c0003t0006g0030 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+630C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640897 | |||||||
chr17:3640958 | G | C | 1 | a0001c0003t0009g0188 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.61+691G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3640958 | |||||||
chr17:3641001 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(94): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+734A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641001 | |||||||
chr17:3641019 | G | A | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+752G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641019 | |||||||
chr17:3641019 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.61+752G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641019 | |||||||
chr17:3641111 | G | T | 1 | a0001c0001t0028g0029 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.61+844G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641111 | |||||||
chr17:3641355 | G | GATATATA others(13): Show |
1 | a0002c0002t0011g0258 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.61+1091_61+1092ins others(20): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641355 | ||||||
chr17:3641355 | GATAC | G | 6 | a0001c0001t0002g0056 a0001c0001t0005g0057 a0001c0001t0021g0058 others(3): Show |
6 | HG01516.hp1 HG01952.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+1092_61+1095del others(4): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641355 | ||||||
chr17:3641355 | GATACAT | G | 24 | a0001c0001t0002g0018 a0001c0001t0002g0062 a0001c0001t0002g0064 others(21): Show |
24 | HG00544.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.61+1092_61+1097del others(6): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641355 | ||||||
chr17:3641355 | GATACATA others(1): Show |
G | 16 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0043 others(13): Show |
26 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.61+1092_61+1099del others(8): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641355 | ||||||
chr17:3641357 | T | G | 53 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0005 others(50): Show |
66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.61+1090T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641357 | |||||||
chr17:3641359 | C | CAT | 3 | a0001c0001t0006g0031 a0001c0003t0047g0219 a0002c0008t0071g0261 |
3 | HG00544.hp1 HG03098.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.61+1117_61+1118dup others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(3): Show |
2 | a0001c0001t0045g0249 a0002c0002t0053g0250 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.61+1109_61+1118dup others(10): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(7): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0003t0001g0154 |
3 | HG02015.hp1 HG02040.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.61+1105_61+1118dup others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(9): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0152 a0001c0001t0001g0160 others(4): Show |
8 | HG02647.hp1 HG02735.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+1103_61+1118dup others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0169 others(1): Show |
4 | HG02056.hp1 HG02273.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+1101_61+1118dup others(18): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(13): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0153 a0001c0001t0001g0157 |
4 | HG00423.hp2 HG01952.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1099_61+1118dup others(20): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(15): Show |
3 | a0001c0001t0007g0172 a0001c0001t0065g0163 a0001c0001t0073g0175 |
3 | HG02698.hp2 HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.61+1097_61+1118dup others(22): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(17): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0003c0005t0008g0266 |
3 | HG01074.hp1 HG01517.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.61+1095_61+1118dup others(24): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(19): Show |
1 | a0001c0001t0007g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+1093_61+1118dup others(26): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(21): Show |
1 | a0001c0001t0007g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(28): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | CATATATA others(23): Show |
1 | a0001c0001t0080g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(30): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641359 | ||||||
chr17:3641359 | C | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0111 a0003c0005t0008g0047 others(2): Show |
5 | HG02559.hp2 HG03130.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1092C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641359 | |||||||
chr17:3641359 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
75 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.61+1092C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641359 | |||||||
chr17:3641360 | A | C | 1 | a0001c0001t0001g0006 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.61+1093A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641360 | |||||||
chr17:3641361 | T | G | 6 | a0001c0001t0002g0056 a0001c0001t0005g0057 a0001c0001t0021g0058 others(3): Show |
6 | HG01516.hp1 HG01952.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+1094T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641361 | |||||||
chr17:3641363 | T | G | 24 | a0001c0001t0002g0018 a0001c0001t0002g0062 a0001c0001t0002g0064 others(21): Show |
24 | HG00544.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.61+1096T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641363 | |||||||
chr17:3641365 | T | G | 17 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0043 others(14): Show |
27 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.61+1098T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641365 | |||||||
chr17:3641373 | TATATATA | T | 32 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0005 others(29): Show |
36 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.61+1107_61+1113del others(7): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641373 | |||||||
chr17:3641373 | TATATATA others(2): Show |
T | 5 | a0001c0001t0002g0085 a0001c0001t0007g0014 a0001c0001t0015g0014 others(2): Show |
5 | HG01081.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1107_61+1115del others(9): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641373 | |||||||
chr17:3641374 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0085g0170 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61+1109_61+1121del others(13): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641374 | ||||||
chr17:3641374 | ATATATAT others(7): Show |
A | 1 | a0001c0003t0036g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.61+1109_61+1122del others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641374 | ||||||
chr17:3641375 | TATATATA | T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(4): Show |
9 | HG01496.hp1 NA18960.hp1 NA18988.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+1109_61+1115del others(7): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641375 | |||||||
chr17:3641377 | TATATA | T | 3 | a0003c0005t0008g0047 a0003c0005t0008g0048 a0003c0005t0008g0049 |
3 | HG02559.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+1111_61+1115del others(5): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641377 | |||||||
chr17:3641378 | A | AT | 2 | a0002c0002t0004g0034 a0002c0002t0010g0225 |
3 | HG00323.hp2 HG02683.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.61+1112dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641378 | ||||||
chr17:3641378 | A | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0070 a0001c0001t0005g0057 |
3 | HG01516.hp1 HG01952.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.61+1111A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641378 | |||||||
chr17:3641378 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0171 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.61+1113_61+1124del others(12): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641378 | ||||||
chr17:3641380 | A | T | 21 | a0001c0001t0002g0018 a0001c0001t0002g0056 a0001c0001t0002g0064 others(18): Show |
22 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.61+1113A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641380 | |||||||
chr17:3641382 | A | AT | 8 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(5): Show |
8 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+1116dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641382 | ||||||
chr17:3641382 | A | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(69): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.61+1115A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641382 | |||||||
chr17:3641382 | ATATTT | A | 12 | a0001c0001t0006g0211 a0001c0003t0006g0232 a0001c0003t0009g0003 others(9): Show |
13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+1117_61+1121del others(5): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641382 | ||||||
chr17:3641384 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18993.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(15): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0006 a0002c0002t0032g0255 |
2 | NA18947.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(17): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0006 a0001c0001t0082g0179 |
2 | HG02080.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(19): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(14): Show |
6 | a0001c0001t0001g0006 a0001c0001t0031g0168 a0001c0001t0074g0028 others(3): Show |
6 | HG03942.hp1 NA18968.hp1 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(21): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(16): Show |
1 | a0002c0002t0014g0254 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(23): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0006 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(25): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(23): Show |
1 | a0001c0001t0075g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(30): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(29): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(25): Show |
1 | a0001c0004t0054g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(32): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(23): Show |
1 | a0001c0001t0015g0028 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(30): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(18): Show |
1 | a0002c0002t0034g0038 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(25): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(15): Show |
1 | a0002c0002t0011g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(22): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(16): Show |
2 | a0002c0002t0019g0252 a0002c0002t0019g0256 |
2 | NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(23): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0006 a0001c0004t0057g0264 |
2 | NA18906.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(24): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0006 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(21): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(15): Show |
1 | a0001c0004t0055g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(22): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(16): Show |
1 | a0001c0004t0018g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(23): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(11): Show |
2 | a0001c0004t0025g0039 a0001c0004t0025g0265 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(18): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(15): Show |
1 | a0001c0004t0018g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(22): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(16): Show |
1 | a0002c0002t0004g0237 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(23): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(17): Show |
1 | a0001c0004t0018g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(24): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(14): Show |
2 | a0002c0002t0004g0001 a0002c0002t0070g0234 |
2 | HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(21): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(8): Show |
3 | a0002c0002t0004g0001 a0002c0002t0004g0239 a0002c0002t0010g0001 |
3 | HG01243.hp2 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(15): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(10): Show |
2 | a0002c0002t0004g0001 a0002c0002t0004g0041 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(17): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(7): Show |
1 | a0002c0002t0004g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(8): Show |
2 | a0002c0002t0004g0001 a0002c0002t0004g0240 |
7 | HG02486.hp1 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(15): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(9): Show |
6 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0235 others(3): Show |
7 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(7): Show |
1 | a0002c0002t0004g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATAT others(9): Show |
1 | a0002c0002t0004g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | ATATATTT others(9): Show |
1 | a0002c0002t0004g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | A | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(94): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.61+1117A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641384 | |||||||
chr17:3641384 | AT | A | 10 | a0001c0001t0003g0007 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
15 | NA18944.hp1 NA18945.hp1 NA18956.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+1142delT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | ATTT | A | 8 | a0001c0001t0003g0199 a0001c0001t0049g0198 a0001c0003t0003g0183 others(5): Show |
8 | HG00423.hp1 HG01981.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+1140_61+1142del others(3): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641384 | ATTTTT | A | 23 | a0001c0001t0003g0182 a0001c0001t0006g0210 a0001c0001t0022g0212 others(20): Show |
28 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.61+1138_61+1142del others(5): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3641384 | ||||||
chr17:3641385 | T | TA | 5 | a0001c0001t0001g0115 a0001c0001t0001g0164 a0001c0001t0003g0189 others(2): Show |
5 | HG00323.hp1 HG02683.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(1): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(4): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0083g0148 others(1): Show |
4 | HG01081.hp1 HG01928.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(11): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(6): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0020g0177 |
3 | HG02040.hp1 NA19062.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(13): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(8): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0138 a0001c0001t0001g0144 others(4): Show |
9 | HG01358.hp2 NA18968.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(15): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(10): Show |
13 | a0001c0001t0001g0026 a0001c0001t0001g0127 a0001c0001t0001g0128 others(10): Show |
13 | HG00621.hp1 HG02698.hp1 HG03492.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(17): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(12): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0129 others(6): Show |
12 | HG01099.hp2 HG01496.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(19): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.61+1118_61+1119ins others(21): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(16): Show |
9 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0122 others(6): Show |
9 | HG00621.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(23): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(18): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0114 a0001c0001t0020g0120 others(1): Show |
5 | HG01516.hp2 HG02004.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(25): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641385 | T | TATATATA others(36): Show |
1 | a0001c0001t0001g0021 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61+1118_61+1119ins others(43): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641385 | |||||||
chr17:3641386 | T | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0150 others(26): Show |
35 | HG00423.hp2 HG00544.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.61+1119T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641386 | |||||||
chr17:3641387 | T | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0118 others(26): Show |
36 | HG00323.hp1 HG01123.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.61+1120T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641387 | |||||||
chr17:3641388 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0152 others(16): Show |
24 | HG00423.hp2 HG00544.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.61+1121T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641388 | |||||||
chr17:3641389 | T | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0127 others(21): Show |
30 | HG00323.hp1 HG00423.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.61+1122T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641389 | |||||||
chr17:3641390 | T | A | 10 | a0001c0001t0001g0150 a0001c0001t0003g0031 a0001c0001t0006g0031 others(7): Show |
12 | HG00544.hp1 HG01517.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.61+1123T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641390 | |||||||
chr17:3641391 | T | A | 6 | a0001c0001t0003g0191 a0001c0001t0086g0121 a0001c0003t0003g0017 others(3): Show |
7 | HG04228.hp1 NA18945.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+1124T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641391 | |||||||
chr17:3641392 | T | A | 2 | a0001c0001t0028g0029 a0001c0003t0047g0219 |
3 | HG01891.hp1 HG03041.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.61+1125T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641392 | |||||||
chr17:3641393 | T | A | 1 | a0001c0003t0033g0190 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.61+1126T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641393 | |||||||
chr17:3641394 | T | A | 1 | a0002c0002t0011g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.61+1127T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641394 | |||||||
chr17:3641395 | T | A | 1 | a0002c0002t0019g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.61+1128T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641395 | |||||||
chr17:3641403 | T | A | 15 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(12): Show |
15 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+1136T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641403 | |||||||
chr17:3641435 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(95): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+1168A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641435 | |||||||
chr17:3641455 | G | A | 1 | a0001c0003t0016g0184 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.61+1188G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641455 | |||||||
chr17:3641485 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(95): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+1218G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641485 | |||||||
chr17:3641541 | G | A | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+1274G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641541 | |||||||
chr17:3641627 | G | A | 1 | a0001c0001t0007g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+1360G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641627 | |||||||
chr17:3641801 | A | G | 1 | a0001c0003t0003g0216 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.61+1534A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641801 | |||||||
chr17:3641818 | G | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(111): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.61+1551G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641818 | |||||||
chr17:3641833 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(95): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+1566G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641833 | |||||||
chr17:3641939 | G | A | 4 | a0001c0001t0044g0251 a0001c0001t0045g0249 a0002c0002t0053g0250 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+1672G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3641939 | |||||||
chr17:3642008 | T | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(111): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.61+1741T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642008 | |||||||
chr17:3642021 | G | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(111): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.61+1754G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642021 | |||||||
chr17:3642029 | A | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(111): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.61+1762A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642029 | |||||||
chr17:3642041 | C | CTGTGTGT others(1): Show |
16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.61+1782_61+1789dup others(8): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0040g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.61+1780_61+1789dup others(10): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(5): Show |
4 | a0001c0001t0002g0078 a0001c0001t0037g0108 a0001c0001t0041g0079 others(1): Show |
4 | HG02055.hp2 HG02071.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+1778_61+1789dup others(12): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(7): Show |
11 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(8): Show |
13 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+1776_61+1789dup others(14): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(9): Show |
72 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(69): Show |
92 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.61+1789_61+1790ins others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(11): Show |
9 | a0001c0001t0002g0070 a0001c0001t0002g0094 a0001c0001t0002g0095 others(6): Show |
10 | HG00280.hp2 HG01884.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+1789_61+1790ins others(18): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0005g0053 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.61+1789_61+1790ins others(20): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642041 | CTGTGTGT others(19): Show |
C | 1 | a0001c0001t0084g0142 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.61+1790_61+1815del others(26): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642041 | ||||||
chr17:3642057 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0068g0097 |
3 | HG03927.hp1 NA18989.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.61+1790A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642057 | |||||||
chr17:3642058 | C | T | 1 | a0001c0001t0068g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+1791C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642058 | |||||||
chr17:3642059 | C | G | 1 | a0001c0001t0068g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+1792C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642059 | |||||||
chr17:3642060 | C | T | 1 | a0001c0001t0068g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+1793C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642060 | |||||||
chr17:3642062 | G | T | 1 | a0001c0001t0068g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+1795G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642062 | |||||||
chr17:3642064 | C | CGT | 23 | a0001c0001t0005g0125 a0001c0001t0007g0116 a0001c0001t0007g0117 others(20): Show |
37 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+1815_61+1816dup others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642064 | C | CGTGTGT | 75 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(72): Show |
97 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.61+1811_61+1816dup others(6): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642064 | C | CGTGTGTG others(1): Show |
21 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0076 others(18): Show |
21 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.61+1809_61+1816dup others(8): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642064 | C | CGTGTGTG others(3): Show |
16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
18 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+1807_61+1816dup others(10): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642064 | C | CGTGTGTG others(5): Show |
2 | a0003c0005t0008g0046 a0003c0005t0008g0049 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+1805_61+1816dup others(12): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642064 | C | T | 1 | a0001c0001t0068g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61+1797C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642064 | |||||||
chr17:3642064 | CGTGT | C | 4 | a0001c0001t0037g0108 a0001c0004t0018g0016 a0001c0004t0054g0105 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+1813_61+1816del others(4): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642064 | ||||||
chr17:3642142 | C | CGT | 34 | a0001c0001t0020g0227 a0001c0001t0022g0194 a0001c0003t0003g0181 others(31): Show |
50 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.61+1897_61+1898dup others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642142 | ||||||
chr17:3642142 | C | CGTGT | 10 | a0001c0001t0037g0108 a0001c0004t0054g0105 a0001c0004t0056g0107 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+1895_61+1898dup others(4): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642142 | ||||||
chr17:3642142 | C | CGTGTGT | 15 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(12): Show |
18 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+1893_61+1898dup others(6): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642142 | ||||||
chr17:3642142 | CGT | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(79): Show |
98 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.61+1897_61+1898del others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642142 | ||||||
chr17:3642142 | CGTGTGTG others(1): Show |
C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(74): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.61+1891_61+1898del others(8): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3642142 | ||||||
chr17:3642190 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.61+1923A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642190 | |||||||
chr17:3642235 | A | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(112): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.61+1968A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642235 | |||||||
chr17:3642265 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(112): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.61+1998T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642265 | |||||||
chr17:3642392 | A | G | 1 | a0001c0001t0081g0130 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.61+2125A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642392 | |||||||
chr17:3642426 | G | A | 1 | a0002c0002t0070g0234 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61+2159G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642426 | |||||||
chr17:3642516 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(79): Show |
98 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.61+2249C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642516 | |||||||
chr17:3642517 | G | A | 1 | a0002c0002t0007g0241 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.61+2250G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642517 | |||||||
chr17:3642557 | A | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(195): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.61+2290A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642557 | |||||||
chr17:3642645 | G | A | 1 | a0001c0001t0021g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.61+2378G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642645 | |||||||
chr17:3642829 | T | A | 1 | a0002c0002t0010g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.61+2562T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642829 | |||||||
chr17:3642866 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
100 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.61+2599G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642866 | |||||||
chr17:3642901 | C | G | 2 | a0001c0004t0018g0016 a0001c0004t0054g0105 |
4 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+2634C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642901 | |||||||
chr17:3642937 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(276): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.61+2670T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3642937 | |||||||
chr17:3643053 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(112): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.61+2786G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643053 | |||||||
chr17:3643116 | T | C | 14 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(11): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+2849T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643116 | |||||||
chr17:3643182 | C | T | 18 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(15): Show |
18 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+2915C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643182 | |||||||
chr17:3643183 | G | A | 1 | a0001c0003t0017g0203 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.61+2916G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643183 | |||||||
chr17:3643345 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.61+3078T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643345 | |||||||
chr17:3643371 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61+3104G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643371 | |||||||
chr17:3643464 | C | T | 1 | a0001c0001t0085g0170 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61+3197C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643464 | |||||||
chr17:3643469 | C | T | 1 | a0001c0003t0003g0222 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.61+3202C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643469 | |||||||
chr17:3643592 | TCTCA | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(74): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.61+3330_61+3333del others(4): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3643592 | ||||||
chr17:3643811 | A | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(118): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.61+3544A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643811 | |||||||
chr17:3643846 | C | T | 1 | a0001c0001t0064g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.61+3579C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643846 | |||||||
chr17:3643892 | T | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(116): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.62-3552T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3643892 | |||||||
chr17:3644001 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.62-3443T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644001 | |||||||
chr17:3644200 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.62-3244A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644200 | |||||||
chr17:3644286 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.62-3158G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644286 | |||||||
chr17:3644289 | C | T | 1 | a0001c0001t0043g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.62-3155C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644289 | |||||||
chr17:3644339 | C | T | 1 | a0001c0003t0003g0201 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.62-3105C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644339 | |||||||
chr17:3644538 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.62-2906C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644538 | |||||||
chr17:3644610 | G | A | 2 | a0001c0003t0003g0197 a0001c0003t0006g0196 |
2 | NA18943.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.62-2834G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644610 | |||||||
chr17:3644905 | A | G | 13 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(10): Show |
27 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.62-2539A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644905 | |||||||
chr17:3644986 | G | A | 1 | a0002c0002t0004g0034 | 2 | HG02683.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.62-2458G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3644986 | |||||||
chr17:3645039 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0159 |
3 | NA18961.hp2 NA18962.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.62-2405T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645039 | |||||||
chr17:3645131 | T | C | 1 | a0001c0001t0005g0081 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.62-2313T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645131 | |||||||
chr17:3645153 | A | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(118): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.62-2291A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645153 | |||||||
chr17:3645168 | C | A | 1 | a0001c0001t0005g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.62-2276C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645168 | |||||||
chr17:3645219 | GAGGCTCC others(9): Show |
G | 1 | a0001c0001t0077g0074 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.62-2221_62-2206del others(16): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3645219 | ||||||
chr17:3645353 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(118): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.62-2091C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645353 | |||||||
chr17:3645395 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(118): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.62-2049G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645395 | |||||||
chr17:3645451 | G | A | 1 | a0001c0001t0041g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.62-1993G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645451 | |||||||
chr17:3645490 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(74): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.62-1954C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645490 | |||||||
chr17:3645512 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.62-1932C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645512 | |||||||
chr17:3645535 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
99 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.62-1909G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645535 | |||||||
chr17:3645612 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.62-1832C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645612 | |||||||
chr17:3645859 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0123 others(33): Show |
41 | HG01433.hp2 HG01928.hp1 HG01928.hp2 others(38): Show |
intron_variant | MODIFIER | c.62-1565dupA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3645859 | ||||||
chr17:3645859 | CA | C | 70 | a0001c0001t0002g0069 a0001c0001t0002g0100 a0001c0001t0003g0007 others(67): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.62-1565delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3645859 | ||||||
chr17:3645933 | G | C | 1 | a0001c0004t0018g0016 | 3 | HG02257.hp2 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-1511G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645933 | |||||||
chr17:3645945 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0145 |
2 | NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.62-1499T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645945 | |||||||
chr17:3645965 | GA | G | 16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-1477delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3645965 | ||||||
chr17:3645974 | C | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.62-1470C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3645974 | |||||||
chr17:3645975 | TG | T | 105 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(102): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.62-1463delG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3645975 | ||||||
chr17:3646003 | C | T | 1 | a0001c0001t0080g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-1441C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646003 | |||||||
chr17:3646006 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(81): Show |
101 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.62-1438G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646006 | |||||||
chr17:3646176 | T | C | 182 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(179): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.62-1268T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646176 | |||||||
chr17:3646292 | C | CT | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.62-1136dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3646292 | ||||||
chr17:3646292 | C | CTT | 10 | a0001c0001t0001g0144 a0001c0001t0001g0169 a0001c0001t0002g0066 others(7): Show |
10 | HG01358.hp1 HG01433.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-1137_62-1136dup others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3646292 | ||||||
chr17:3646296 | T | C | 2 | a0001c0004t0018g0016 a0001c0004t0054g0105 |
4 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1148T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646296 | |||||||
chr17:3646321 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0013 others(14): Show |
21 | HG02155.hp2 NA18947.hp1 NA18949.hp2 others(18): Show |
intron_variant | MODIFIER | c.62-1123C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646321 | |||||||
chr17:3646532 | C | G | 7 | a0001c0003t0003g0030 a0001c0003t0003g0183 a0001c0003t0006g0030 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-912C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646532 | |||||||
chr17:3646577 | A | G | 18 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(15): Show |
18 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.62-867A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646577 | |||||||
chr17:3646788 | T | TG | 273 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(270): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.62-651dupG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 3646788 | ||||||
chr17:3646869 | T | A | 1 | a0001c0004t0018g0016 | 3 | HG02257.hp2 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-575T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646869 | |||||||
chr17:3646990 | C | G | 16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-454C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3646990 | |||||||
chr17:3647102 | C | T | 16 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(13): Show |
19 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-342C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3647102 | |||||||
chr17:3647114 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(280): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.62-330A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3647114 | |||||||
chr17:3647220 | C | T | 17 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(14): Show |
17 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-224C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3647220 | |||||||
chr17:3647226 | G | A | 1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62-218G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 3/11 | chr17 | 3647226 | |||||||
chr17:3647829 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.140+307C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3647829 | |||||||
chr17:3647884 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.140+362A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3647884 | |||||||
chr17:3647983 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.140+461C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3647983 | |||||||
chr17:3648013 | C | T | 1 | a0001c0001t0065g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.140+491C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648013 | |||||||
chr17:3648016 | C | T | 61 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(58): Show |
73 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.140+494C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648016 | |||||||
chr17:3648033 | T | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(263): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.140+511T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648033 | |||||||
chr17:3648051 | T | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(81): Show |
101 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.140+529T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648051 | |||||||
chr17:3648160 | C | G | 1 | a0007c0006t0003g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.140+638C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648160 | |||||||
chr17:3648279 | T | A | 4 | a0001c0003t0009g0188 a0001c0003t0017g0208 a0001c0003t0017g0231 others(1): Show |
4 | HG01361.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-568T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648279 | |||||||
chr17:3648292 | C | T | 2 | a0001c0004t0025g0039 a0001c0004t0055g0039 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.141-555C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648292 | |||||||
chr17:3648505 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0031g0168 |
2 | NA18943.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.141-342C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648505 | |||||||
chr17:3648529 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.141-318C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648529 | |||||||
chr17:3648685 | T | C | 1 | a0001c0003t0050g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.141-162T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648685 | |||||||
chr17:3648687 | C | T | 1 | a0001c0004t0057g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.141-160C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648687 | |||||||
chr17:3648704 | C | T | 2 | a0002c0002t0019g0252 a0002c0002t0019g0256 |
2 | NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.141-143C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648704 | |||||||
chr17:3648744 | G | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(74): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.141-103G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648744 | |||||||
chr17:3648794 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.141-53T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648794 | |||||||
chr17:3648795 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.141-52G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648795 | |||||||
chr17:3648796 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.141-51A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 4/11 | chr17 | 3648796 | |||||||
chr17:3649078 | G | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(81): Show |
101 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.225+147G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649078 | |||||||
chr17:3649172 | G | A | 1 | a0001c0001t0088g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.225+241G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649172 | |||||||
chr17:3649238 | A | G | 10 | a0001c0001t0037g0108 a0001c0004t0018g0016 a0001c0004t0025g0039 others(7): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.225+307A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649238 | |||||||
chr17:3649291 | T | G | 2 | a0001c0001t0013g0112 a0001c0001t0013g0113 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.225+360T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649291 | |||||||
chr17:3649433 | C | T | 61 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(58): Show |
73 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.225+502C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649433 | |||||||
chr17:3649451 | C | CA | 11 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0005g0084 others(8): Show |
11 | HG01109.hp1 HG01433.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+539dupA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3649451 | ||||||
chr17:3649451 | CA | C | 99 | a0001c0001t0001g0143 a0001c0001t0002g0066 a0001c0001t0003g0007 others(96): Show |
117 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.225+539delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3649451 | ||||||
chr17:3649451 | CAA | C | 7 | a0001c0001t0003g0199 a0001c0003t0047g0219 a0003c0005t0008g0046 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+538_225+539del others(2): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3649451 | ||||||
chr17:3649456 | A | G | 14 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(11): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.225+525A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649456 | |||||||
chr17:3649457 | A | G | 5 | a0001c0001t0043g0093 a0003c0005t0008g0046 a0003c0005t0008g0047 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+526A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649457 | |||||||
chr17:3649596 | A | G | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+665A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649596 | |||||||
chr17:3649611 | T | A | 1 | a0002c0008t0071g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.225+680T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649611 | |||||||
chr17:3649718 | C | A | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+787C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649718 | |||||||
chr17:3649764 | C | CT | 145 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(142): Show |
174 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.225+835dupT | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3649764 | ||||||
chr17:3649892 | T | C | 1 | a0002c0008t0071g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.225+961T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649892 | |||||||
chr17:3649976 | A | G | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+1045A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649976 | |||||||
chr17:3649998 | A | C | 4 | a0001c0003t0003g0181 a0001c0003t0003g0230 a0002c0002t0004g0034 others(1): Show |
5 | HG00099.hp2 HG00323.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+1067A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3649998 | |||||||
chr17:3650136 | A | G | 11 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0189 others(8): Show |
15 | HG00323.hp1 HG00544.hp1 NA18944.hp1 others(12): Show |
intron_variant | MODIFIER | c.225+1205A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650136 | |||||||
chr17:3650157 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0132 |
2 | NA19067.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.225+1226A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650157 | |||||||
chr17:3650180 | G | A | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+1249G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650180 | |||||||
chr17:3650232 | A | G | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.225+1301A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650232 | |||||||
chr17:3650288 | G | A | 2 | a0003c0005t0008g0046 a0003c0005t0008g0049 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.225+1357G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650288 | |||||||
chr17:3650361 | A | G | 14 | a0001c0001t0020g0227 a0001c0003t0003g0181 a0001c0003t0003g0230 others(11): Show |
16 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.225+1430A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650361 | |||||||
chr17:3650371 | A | G | 17 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(14): Show |
17 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.225+1440A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650371 | |||||||
chr17:3650449 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.225+1518T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650449 | |||||||
chr17:3650715 | G | A | 17 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(14): Show |
17 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.225+1784G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650715 | |||||||
chr17:3650765 | G | A | 186 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(183): Show |
219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.225+1834G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650765 | |||||||
chr17:3650838 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.225+1907T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650838 | |||||||
chr17:3650888 | T | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+1957T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3650888 | |||||||
chr17:3651001 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.225+2070C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651001 | |||||||
chr17:3651258 | C | G | 17 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(14): Show |
17 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.225+2327C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651258 | |||||||
chr17:3651337 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.225+2406C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651337 | |||||||
chr17:3651375 | G | A | 253 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(250): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.225+2444G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651375 | |||||||
chr17:3651377 | C | T | 1 | a0001c0004t0056g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.225+2446C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651377 | |||||||
chr17:3651427 | A | G | 1 | a0003c0005t0008g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.225+2496A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651427 | |||||||
chr17:3651518 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0087g0140 |
2 | NA18970.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.225+2587C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651518 | |||||||
chr17:3651523 | G | A | 12 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(9): Show |
12 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+2592G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651523 | |||||||
chr17:3651700 | C | G | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.225+2769C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651700 | |||||||
chr17:3651702 | TG | T | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+2774delG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651702 | ||||||
chr17:3651706 | A | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+2775A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651706 | |||||||
chr17:3651708 | T | G | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.225+2777T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651708 | |||||||
chr17:3651827 | G | A | 1 | a0001c0001t0021g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.225+2896G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651827 | |||||||
chr17:3651973 | C | CAA | 17 | a0002c0002t0011g0038 a0002c0002t0011g0243 a0002c0002t0011g0253 others(14): Show |
17 | HG00621.hp2 HG02135.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.226-3017_226-3016d others(4): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651973 | C | CAAAA | 72 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(69): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.226-3019_226-3016d others(6): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651973 | C | CAAAAA | 69 | a0001c0001t0002g0050 a0001c0001t0002g0066 a0001c0001t0002g0110 others(66): Show |
81 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.226-3020_226-3016d others(7): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651973 | C | CAAAAAA | 11 | a0001c0001t0001g0114 a0001c0001t0001g0145 a0001c0001t0001g0159 others(8): Show |
12 | HG01070.hp2 HG01891.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-3021_226-3016d others(8): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651973 | C | CAAAAAAA | 102 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(99): Show |
120 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.226-3022_226-3016d others(9): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651973 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0118 a0001c0001t0001g0138 a0001c0001t0001g0141 others(4): Show |
7 | HG01123.hp1 HG01358.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-3023_226-3016d others(10): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651973 | ||||||
chr17:3651978 | A | AAAAAG | 17 | a0001c0001t0044g0251 a0001c0001t0045g0249 a0002c0002t0004g0001 others(14): Show |
31 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.226-3004_226-3000d others(7): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3651978 | ||||||
chr17:3651983 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(259): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.226-3015G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651983 | |||||||
chr17:3651994 | A | T | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-3004A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651994 | |||||||
chr17:3651995 | A | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-3003A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3651995 | |||||||
chr17:3652096 | A | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-2902A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652096 | |||||||
chr17:3652130 | G | A | 61 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(58): Show |
73 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.226-2868G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652130 | |||||||
chr17:3652145 | G | A | 1 | a0001c0001t0028g0029 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.226-2853G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652145 | |||||||
chr17:3652330 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.226-2668G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652330 | |||||||
chr17:3652345 | A | G | 1 | a0002c0002t0004g0228 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.226-2653A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652345 | |||||||
chr17:3652358 | G | A | 17 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(14): Show |
17 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.226-2640G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652358 | |||||||
chr17:3652453 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.226-2545G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652453 | |||||||
chr17:3652523 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.226-2475C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652523 | |||||||
chr17:3652541 | G | A | 1 | a0002c0002t0004g0228 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.226-2457G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652541 | |||||||
chr17:3652692 | T | C | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.226-2306T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652692 | |||||||
chr17:3652826 | T | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-2172T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652826 | |||||||
chr17:3652846 | T | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-2152T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652846 | |||||||
chr17:3652856 | A | AC | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-2141dupC | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3652856 | ||||||
chr17:3652866 | G | T | 1 | a0001c0001t0006g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.226-2132G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652866 | |||||||
chr17:3652899 | T | G | 1 | a0002c0002t0011g0260 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.226-2099T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3652899 | |||||||
chr17:3653152 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.226-1846C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653152 | |||||||
chr17:3653162 | A | G | 5 | a0001c0003t0003g0011 a0001c0003t0003g0216 a0001c0003t0006g0011 others(2): Show |
7 | HG00558.hp1 NA18961.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1836A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653162 | |||||||
chr17:3653169 | T | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-1829T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653169 | |||||||
chr17:3653269 | T | C | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.226-1729T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653269 | |||||||
chr17:3653300 | C | T | 71 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(68): Show |
86 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.226-1698C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653300 | |||||||
chr17:3653301 | T | C | 1 | a0001c0001t0084g0142 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.226-1697T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653301 | |||||||
chr17:3653306 | A | G | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-1692A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653306 | |||||||
chr17:3653329 | C | G | 3 | a0001c0003t0016g0184 a0001c0003t0016g0185 a0001c0003t0016g0187 |
3 | NA18747.hp1 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.226-1669C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653329 | |||||||
chr17:3653488 | A | G | 1 | a0001c0001t0086g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.226-1510A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653488 | |||||||
chr17:3653559 | C | A | 1 | a0002c0002t0019g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.226-1439C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653559 | |||||||
chr17:3653560 | C | G | 1 | a0002c0002t0019g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.226-1438C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653560 | |||||||
chr17:3653603 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(68): Show |
91 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.226-1395C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653603 | |||||||
chr17:3653626 | A | G | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-1372A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653626 | |||||||
chr17:3653705 | G | C | 1 | a0001c0003t0003g0201 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.226-1293G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653705 | |||||||
chr17:3653761 | A | T | 3 | a0001c0003t0003g0017 a0001c0003t0033g0017 a0001c0003t0033g0190 |
4 | NA18945.hp1 NA18992.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1237A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653761 | |||||||
chr17:3653837 | T | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-1161T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653837 | |||||||
chr17:3653881 | G | GA | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.226-1112dupA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3653881 | ||||||
chr17:3653887 | T | A | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.226-1111T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653887 | |||||||
chr17:3653925 | T | C | 3 | a0001c0003t0003g0017 a0001c0003t0033g0017 a0001c0003t0033g0190 |
4 | NA18945.hp1 NA18992.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1073T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3653925 | |||||||
chr17:3654088 | A | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.226-910A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654088 | |||||||
chr17:3654201 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(75): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.226-797A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654201 | |||||||
chr17:3654205 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
99 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.226-793C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654205 | |||||||
chr17:3654243 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.226-755C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654243 | |||||||
chr17:3654300 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.226-698A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654300 | |||||||
chr17:3654302 | G | C | 2 | a0001c0003t0003g0197 a0001c0003t0006g0196 |
2 | NA18943.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.226-696G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654302 | |||||||
chr17:3654307 | C | T | 4 | a0001c0001t0044g0251 a0001c0001t0045g0249 a0002c0002t0053g0250 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-691C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654307 | |||||||
chr17:3654552 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0005g0098 |
2 | HG01516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.226-446T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654552 | |||||||
chr17:3654680 | C | CA | 23 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0002g0002 others(20): Show |
32 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.226-301dupA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3654680 | ||||||
chr17:3654680 | CA | C | 9 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0005g0045 others(6): Show |
9 | HG00544.hp2 HG01167.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-301delA | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 3654680 | ||||||
chr17:3654765 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.226-233C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654765 | |||||||
chr17:3654804 | G | A | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.226-194G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654804 | |||||||
chr17:3654891 | C | T | 4 | a0001c0001t0044g0251 a0001c0001t0045g0249 a0002c0002t0053g0250 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-107C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654891 | |||||||
chr17:3654918 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.226-80C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 5/11 | chr17 | 3654918 | |||||||
chr17:3655123 | C | G | 265 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(262): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.329+22C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 6/11 | chr17 | 3655123 | |||||||
chr17:3655149 | C | T | 2 | a0001c0001t0086g0121 a0001c0001t0088g0151 |
2 | NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.329+48C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 6/11 | chr17 | 3655149 | |||||||
chr17:3655401 | A | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0002g0002 others(74): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.461+49A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655401 | |||||||
chr17:3655404 | G | A | 188 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(185): Show |
222 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.461+52G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655404 | |||||||
chr17:3655406 | G | A | 63 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(60): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.461+54G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655406 | |||||||
chr17:3655422 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG02040.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.461+70C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655422 | |||||||
chr17:3655616 | C | T | 1 | a0001c0001t0005g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.461+264C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655616 | |||||||
chr17:3655667 | G | A | 1 | a0002c0008t0071g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.461+315G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655667 | |||||||
chr17:3655669 | C | A | 19 | a0001c0001t0004g0025 a0001c0001t0013g0015 a0001c0001t0013g0112 others(16): Show |
20 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.461+317C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655669 | |||||||
chr17:3655979 | G | T | 1 | a0001c0004t0054g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.462-508G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3655979 | |||||||
chr17:3656009 | T | G | 22 | a0001c0001t0044g0251 a0001c0001t0045g0249 a0002c0002t0011g0038 others(19): Show |
22 | HG00621.hp2 HG02135.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-478T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656009 | |||||||
chr17:3656047 | T | TGCCAGTC others(149): Show |
1 | a0002c0002t0004g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.462-301_462-300ins others(156): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656047 | ||||||
chr17:3656079 | T | TTCCACCC others(143): Show |
1 | a0001c0001t0052g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.462-280_462-279ins others(150): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656079 | ||||||
chr17:3656101 | CCCCTGCC others(35): Show |
C | 1 | a0007c0006t0003g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.462-378_462-337del others(42): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656101 | ||||||
chr17:3656136 | G | A | 3 | a0001c0003t0003g0011 a0001c0003t0006g0011 a0001c0003t0006g0206 |
5 | NA18970.hp1 NA18971.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-351G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656136 | |||||||
chr17:3656143 | G | GCCCTGCC others(29): Show |
17 | a0001c0001t0002g0070 a0001c0001t0005g0045 a0001c0001t0005g0073 others(14): Show |
19 | HG00323.hp2 HG00408.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.462-331_462-330ins others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656143 | ||||||
chr17:3656143 | G | GCCCTGCC others(29): Show |
1 | a0001c0001t0081g0130 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.462-330_462-295dup others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656143 | ||||||
chr17:3656157 | T | C | 30 | a0001c0001t0002g0070 a0001c0001t0002g0083 a0001c0001t0005g0045 others(27): Show |
34 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.462-330T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656157 | |||||||
chr17:3656157 | T | TTCCACCC others(29): Show |
134 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0072 others(131): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.462-315_462-280dup others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(65): Show |
4 | a0001c0001t0001g0165 a0001c0001t0044g0251 a0002c0002t0014g0259 others(1): Show |
4 | HG02738.hp1 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-280_462-279ins others(72): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(101): Show |
4 | a0003c0005t0008g0046 a0003c0005t0008g0047 a0003c0005t0008g0048 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.462-280_462-279ins others(108): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(137): Show |
1 | a0001c0001t0045g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.462-280_462-279ins others(144): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(173): Show |
1 | a0002c0002t0061g0248 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.462-280_462-279ins others(180): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(353): Show |
1 | a0002c0002t0053g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.462-280_462-279ins others(360): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(143): Show |
1 | a0001c0001t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.462-280_462-279ins others(150): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(185): Show |
12 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0109 others(9): Show |
25 | HG01167.hp2 HG01243.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.462-301_462-300ins others(192): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656157 | T | TTCCACCC others(383): Show |
1 | a0002c0002t0004g0041 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.462-301_462-300ins others(390): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656157 | ||||||
chr17:3656172 | C | CCCTCACC others(102): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0164 |
2 | NA18957.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.462-280_462-279ins others(109): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656172 | ||||||
chr17:3656173 | C | CCTCACCC others(29): Show |
1 | a0001c0003t0003g0216 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.462-280_462-279ins others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656173 | ||||||
chr17:3656181 | C | CCTGCCAT others(29): Show |
2 | a0001c0001t0041g0079 a0001c0001t0048g0059 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.462-300_462-265dup others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656181 | ||||||
chr17:3656181 | C | CCTGCCAT others(65): Show |
1 | a0001c0001t0021g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.462-265_462-264ins others(72): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656181 | ||||||
chr17:3656187 | ATGCCCCT others(29): Show |
A | 1 | a0001c0001t0022g0194 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.462-284_462-249del others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656187 | ||||||
chr17:3656193 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.462-294C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656193 | |||||||
chr17:3656197 | A | ACCCCCCG others(31): Show |
1 | a0002c0002t0007g0241 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.462-285_462-284ins others(38): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656197 | ||||||
chr17:3656208 | T | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(102): Show |
126 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.462-279T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656208 | |||||||
chr17:3656212 | T | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(102): Show |
126 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.462-275T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656212 | |||||||
chr17:3656217 | A | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(107): Show |
131 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.462-270A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656217 | |||||||
chr17:3656223 | C | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(119): Show |
147 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.462-264C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656223 | |||||||
chr17:3656233 | AC | A | 5 | a0001c0003t0006g0214 a0001c0003t0016g0184 a0001c0003t0016g0185 others(2): Show |
5 | HG00639.hp2 NA18747.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-248delC | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656233 | ||||||
chr17:3656240 | A | G | 5 | a0001c0003t0006g0214 a0001c0003t0016g0184 a0001c0003t0016g0185 others(2): Show |
5 | HG00639.hp2 NA18747.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-247A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656240 | |||||||
chr17:3656249 | C | T | 3 | a0001c0003t0016g0184 a0001c0003t0016g0185 a0001c0003t0016g0187 |
3 | NA18747.hp1 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.462-238C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656249 | |||||||
chr17:3656311 | C | A | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-176C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656311 | |||||||
chr17:3656318 | A | T | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-169A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656318 | |||||||
chr17:3656333 | T | C | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-154T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656333 | |||||||
chr17:3656337 | T | C | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-150T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656337 | |||||||
chr17:3656341 | C | CACTGCCC others(76): Show |
1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-146_462-145ins others(83): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656341 | |||||||
chr17:3656343 | C | A | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-144C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656343 | |||||||
chr17:3656344 | CACCCTGC others(26): Show |
C | 1 | a0001c0001t0003g0195 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.462-142_462-110del others(33): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656344 | |||||||
chr17:3656345 | A | ACCCTGCC others(29): Show |
1 | a0001c0001t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.462-120_462-119ins others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656345 | ||||||
chr17:3656345 | A | C | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-142A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656345 | |||||||
chr17:3656347 | C | CCTGCCCT others(437): Show |
1 | a0002c0008t0071g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.462-96_462-95insTC others(442): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656347 | ||||||
chr17:3656347 | CCTGCCCT others(29): Show |
C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(284): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.462-95_462-60delCC others(34): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656347 | ||||||
chr17:3656348 | CTGCCCTG others(28): Show |
C | 1 | a0001c0001t0001g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.462-138_462-104del others(35): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656348 | |||||||
chr17:3656355 | GCCCCTCC others(30): Show |
G | 1 | a0001c0001t0005g0019 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.462-128_462-92delC others(36): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656355 | ||||||
chr17:3656360 | T | A | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-127T>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656360 | |||||||
chr17:3656368 | C | T | 1 | a0001c0003t0006g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.462-119C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656368 | |||||||
chr17:3656374 | T | C | 1 | a0001c0001t0022g0212 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.462-113T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656374 | |||||||
chr17:3656378 | C | T | 1 | a0001c0003t0006g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.462-109C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656378 | |||||||
chr17:3656381 | C | CCCCTGCC others(35): Show |
1 | a0001c0003t0006g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.462-105_462-104ins others(42): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656381 | ||||||
chr17:3656381 | C | CCCCTGCC others(237): Show |
1 | a0001c0001t0022g0212 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.462-105_462-104ins others(244): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656381 | ||||||
chr17:3656383 | T | C | 3 | a0001c0001t0022g0212 a0001c0003t0006g0214 a0001c0003t0006g0232 |
3 | HG01192.hp2 HG03831.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.462-104T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656383 | |||||||
chr17:3656383 | T | TCTGCCCT others(195): Show |
1 | a0001c0003t0001g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.462-96_462-95insTC others(200): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656383 | ||||||
chr17:3656383 | T | TCTGCCCT others(404): Show |
1 | a0003c0005t0008g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.462-96_462-95insTC others(409): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656383 | ||||||
chr17:3656383 | TCTGCCCT others(65): Show |
T | 1 | a0002c0002t0014g0254 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.462-95_462-24delCC others(70): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 3656383 | ||||||
chr17:3656392 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(4): Show |
7 | HG00621.hp1 HG02165.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.462-95C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656392 | |||||||
chr17:3656393 | C | T | 14 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0043 others(11): Show |
23 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.462-94C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656393 | |||||||
chr17:3656399 | A | C | 13 | a0001c0001t0001g0123 a0001c0001t0003g0199 a0002c0002t0011g0038 others(10): Show |
13 | HG02135.hp1 HG02165.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.462-88A>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656399 | |||||||
chr17:3656404 | C | T | 1 | a0001c0001t0043g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.462-83C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656404 | |||||||
chr17:3656428 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.462-59T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656428 | |||||||
chr17:3656480 | C | A | 1 | a0002c0002t0007g0035 | 2 | HG01258.hp2 HG01433.hp1 |
splice_region_variant&intron_variant | LOW | c.462-7C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 7/11 | chr17 | 3656480 | |||||||
chr17:3657069 | G | A | 63 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0003g0007 others(60): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.681+274G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657069 | |||||||
chr17:3657076 | CAGGGAGG | C | 2 | a0001c0004t0008g0040 a0003c0005t0008g0266 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.681+293_681+299del others(7): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 3657076 | ||||||
chr17:3657085 | G | C | 1 | a0001c0001t0007g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.681+290G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657085 | |||||||
chr17:3657304 | G | A | 15 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(12): Show |
29 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.681+509G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657304 | |||||||
chr17:3657389 | G | A | 13 | a0001c0004t0018g0016 a0001c0004t0025g0039 a0001c0004t0025g0265 others(10): Show |
15 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.681+594G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657389 | |||||||
chr17:3657416 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.682-589T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657416 | |||||||
chr17:3657458 | T | C | 281 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(278): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.682-547T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657458 | |||||||
chr17:3657693 | G | A | 1 | a0001c0003t0006g0213 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.682-312G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657693 | |||||||
chr17:3657907 | G | A | 11 | a0002c0002t0004g0034 a0002c0002t0004g0228 a0002c0002t0007g0035 others(8): Show |
13 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-98G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657907 | |||||||
chr17:3657939 | C | A | 11 | a0002c0002t0004g0034 a0002c0002t0004g0228 a0002c0002t0007g0035 others(8): Show |
13 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.682-66C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 9/11 | chr17 | 3657939 | |||||||
chr17:3658368 | C | A | 5 | a0001c0001t0005g0045 a0001c0001t0005g0073 a0001c0001t0005g0086 others(2): Show |
5 | HG03017.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+193C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658368 | |||||||
chr17:3658396 | A | G | 1 | a0001c0001t0040g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852+221A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658396 | |||||||
chr17:3658403 | G | A | 16 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(13): Show |
16 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.852+228G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658403 | |||||||
chr17:3658417 | C | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(158): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.852+242C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658417 | |||||||
chr17:3658418 | A | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(158): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.852+243A>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658418 | |||||||
chr17:3658434 | C | G | 28 | a0002c0002t0004g0001 a0002c0002t0004g0034 a0002c0002t0004g0037 others(25): Show |
44 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.852+259C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658434 | |||||||
chr17:3658450 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0077g0074 |
2 | HG01175.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.852+275C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658450 | |||||||
chr17:3658456 | T | C | 26 | a0002c0002t0004g0001 a0002c0002t0004g0034 a0002c0002t0004g0037 others(23): Show |
42 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.852+281T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658456 | |||||||
chr17:3658471 | G | A | 2 | a0002c0002t0019g0252 a0002c0002t0019g0256 |
2 | NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.852+296G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658471 | |||||||
chr17:3658523 | G | A | 4 | a0001c0001t0007g0014 a0001c0001t0015g0014 a0001c0001t0015g0020 others(1): Show |
5 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+348G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658523 | |||||||
chr17:3658548 | C | T | 105 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(102): Show |
133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.852+373C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658548 | |||||||
chr17:3658602 | A | ACTCAGGG others(10): Show |
1 | a0001c0001t0089g0204 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.852+430_852+446dup others(17): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 3658602 | ||||||
chr17:3658662 | C | T | 79 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(76): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.852+487C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658662 | |||||||
chr17:3658667 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0043 |
5 | HG01243.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+492G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658667 | |||||||
chr17:3658720 | T | G | 1 | a0001c0003t0038g0215 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.852+545T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658720 | |||||||
chr17:3658746 | C | G | 74 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0004 others(71): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.852+571C>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658746 | |||||||
chr17:3658844 | C | A | 1 | a0001c0001t0007g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.852+669C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658844 | |||||||
chr17:3658888 | G | A | 272 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.852+713G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658888 | |||||||
chr17:3658902 | G | A | 79 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(76): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.852+727G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658902 | |||||||
chr17:3658906 | T | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(76): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.852+731T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658906 | |||||||
chr17:3658908 | T | C | 79 | a0001c0001t0003g0007 a0001c0001t0003g0031 a0001c0001t0003g0182 others(76): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.852+733T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658908 | |||||||
chr17:3658969 | TG | T | 82 | a0001c0001t0002g0064 a0001c0001t0003g0007 a0001c0001t0003g0031 others(79): Show |
95 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.852+802delG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 3658969 | ||||||
chr17:3658971 | G | C | 1 | a0001c0001t0035g0136 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.852+796G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3658971 | |||||||
chr17:3659111 | G | A | 3 | a0001c0004t0025g0039 a0001c0004t0025g0265 a0001c0004t0055g0039 |
3 | HG02055.hp1 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.853-747G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659111 | |||||||
chr17:3659192 | C | CG | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.853-660dupG | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 3659192 | ||||||
chr17:3659194 | G | GC | 13 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0138 others(10): Show |
14 | HG01070.hp1 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-664_853-663ins others(1): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659194 | |||||||
chr17:3659302 | C | A | 1 | a0001c0001t0086g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853-556C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659302 | |||||||
chr17:3659330 | G | T | 11 | a0002c0002t0004g0034 a0002c0002t0004g0228 a0002c0002t0007g0035 others(8): Show |
13 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-528G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659330 | |||||||
chr17:3659467 | ACATGAAG others(48): Show |
A | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-387_853-333del others(55): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 3659467 | ||||||
chr17:3659593 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-265G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659593 | |||||||
chr17:3659597 | C | CCAGCTAC others(46): Show |
1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-261_853-260ins others(53): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659597 | |||||||
chr17:3659603 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-255T>G | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659603 | |||||||
chr17:3659606 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-252T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659606 | |||||||
chr17:3659607 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853-251G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659607 | |||||||
chr17:3659625 | GGGTGCGG others(22): Show |
G | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-232_853-204del others(29): Show |
CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659625 | |||||||
chr17:3659656 | G | C | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-202G>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659656 | |||||||
chr17:3659658 | T | C | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-200T>C | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659658 | |||||||
chr17:3659659 | G | T | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-199G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659659 | |||||||
chr17:3659715 | C | T | 1 | a0001c0001t0066g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.853-143C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659715 | |||||||
chr17:3659797 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.853-61G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659797 | |||||||
chr17:3659830 | C | T | 1 | a0001c0001t0084g0142 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.853-28C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659830 | |||||||
chr17:3659831 | G | A | 1 | a0001c0001t0039g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.853-27G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 10/11 | chr17 | 3659831 | |||||||
chr17:3659990 | G | A | 14 | a0001c0001t0013g0015 a0001c0001t0013g0112 a0001c0001t0013g0113 others(11): Show |
14 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.970+15G>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3659990 | |||||||
chr17:3660020 | C | T | 15 | a0002c0002t0004g0001 a0002c0002t0004g0037 a0002c0002t0004g0041 others(12): Show |
29 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.970+45C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660020 | |||||||
chr17:3660045 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0004 others(71): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.970+70C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660045 | |||||||
chr17:3660067 | C | A | 1 | a0001c0001t0007g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.970+92C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660067 | |||||||
chr17:3660102 | A | T | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.970+127A>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660102 | |||||||
chr17:3660109 | C | T | 1 | a0001c0004t0005g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.971-127C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660109 | |||||||
chr17:3660154 | C | A | 1 | a0001c0001t0090g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.971-82C>A | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660154 | |||||||
chr17:3660157 | C | T | 1 | a0001c0004t0005g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.971-79C>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660157 | |||||||
chr17:3660193 | G | T | 1 | a0002c0002t0004g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.971-43G>T | CTNS | ENSG00000040531.16 | transcript | ENST00000046640.9 | protein_coding | 11/11 | chr17 | 3660193 |