Item | Value |
---|---|
geneid | 91875 |
ensemblid | ENSG00000136319.12 |
hgncid | 19274 |
symbol | TTC5 |
name | tetratricopeptide repeat domain 5 |
refseq_nuc | NM_138376.3 |
refseq_prot | NP_612385.2 |
ensembl_nuc | ENST00000258821.8 |
ensembl_prot | ENSP00000258821.3 |
mane_status | MANE Select |
chr | chr14 |
start | 20286227 |
end | 20305951 |
strand | - |
ver | v1.2 |
region | chr14:20286227-20305951 |
region5000 | chr14:20281227-20310951 |
regionname0 | TTC5_chr14_20286227_20305951 |
regionname5000 | TTC5_chr14_20281227_20310951 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 440 | 306 | 70 | 58 | 146 | 7 | 24 | 113 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
a0002 | 1/0 | 440 | 96 | 12 | 15 | 45 | 3 | 20 | 34 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
a0003 | 0/0 | 440 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
a0004 | 0/0 | 440 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
a0005 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
a0006 | 0/0 | 440 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | MMADE others(435): Show |
chr14 | 20281227 | 20310951 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1320 | 150 | 17 | 34 | 80 | 5 | 14 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0001c0002 | 0/1 | 1320 | 145 | 45 | 23 | 64 | 2 | 10 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0001c0007 | 0/0 | 1320 | 5 | 5 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0001c0008 | 0/0 | 1320 | 3 | 3 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0001c0009 | 0/0 | 1320 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0001c0012 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0002c0003 | 1/0 | 1320 | 61 | 11 | 5 | 29 | 3 | 12 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0002c0004 | 0/0 | 1320 | 34 | 1 | 10 | 15 | 0 | 8 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0002c0010 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0003c0006 | 0/0 | 1320 | 6 | 6 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0004c0005 | 0/0 | 1320 | 6 | 6 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0005c0013 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 | ||
a0006c0011 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | ATGAT others(1315): Show |
chr14 | 20281227 | 20310951 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4735 | 108 | 10 | 16 | 66 | 5 | 11 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0002 | 0/0 | 4739 | 5 | 0 | 3 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0003 | 0/0 | 4738 | 2 | 0 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0006 | 0/0 | 4734 | 14 | 0 | 8 | 5 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4729): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0011 | 0/0 | 4739 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0012 | 0/0 | 4735 | 4 | 2 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0021 | 0/0 | 4739 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0022 | 0/0 | 4736 | 3 | 2 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4731): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0025 | 0/0 | 4736 | 2 | 0 | 0 | 1 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4731): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0026 | 0/0 | 4736 | 2 | 1 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4731): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0030 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0042 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0043 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0045 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0046 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0001t0047 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0001 | 0/0 | 4735 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0002 | 0/0 | 4739 | 41 | 0 | 7 | 28 | 0 | 6 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0003 | 0/0 | 4738 | 30 | 3 | 6 | 17 | 1 | 3 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0004 | 0/0 | 4739 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0006 | 0/0 | 4734 | 3 | 3 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4729): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0008 | 0/0 | 4739 | 10 | 10 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0009 | 0/1 | 4734 | 9 | 2 | 4 | 0 | 1 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4729): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0010 | 0/0 | 4739 | 8 | 0 | 0 | 8 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0011 | 0/0 | 4739 | 7 | 7 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0014 | 0/0 | 4737 | 2 | 1 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0015 | 0/0 | 4743 | 4 | 0 | 4 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4738): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0017 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0018 | 0/0 | 4737 | 2 | 1 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0019 | 0/0 | 4738 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0020 | 0/0 | 4734 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4729): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0024 | 0/0 | 4739 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0028 | 0/0 | 4739 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0029 | 0/0 | 4739 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0033 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0035 | 0/0 | 4740 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4735): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0036 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0037 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0044 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0048 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0054 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0055 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0056 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0057 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0002t0058 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0001c0007t0004 | 0/0 | 4739 | 5 | 5 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0008t0014 | 0/0 | 4737 | 3 | 3 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0001c0009t0002 | 0/0 | 4739 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0001c0012t0027 | 0/0 | 4740 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4735): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0001 | 0/0 | 4735 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0003 | 0/0 | 4738 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0005 | 1/0 | 4737 | 26 | 0 | 1 | 16 | 1 | 7 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0007 | 0/0 | 4738 | 11 | 8 | 1 | 0 | 0 | 2 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0012 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0016 | 0/0 | 4741 | 4 | 0 | 0 | 4 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4736): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0018 | 0/0 | 4737 | 2 | 0 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0023 | 0/0 | 4737 | 3 | 0 | 1 | 0 | 2 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0031 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0032 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0034 | 0/0 | 4739 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0041 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0050 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0051 | 0/0 | 4741 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4736): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0052 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4732): Show |
chr14 | 20281227 | 20310951 |
a0002c0003t0053 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0004 | 0/0 | 4739 | 29 | 1 | 8 | 13 | 0 | 7 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0027 | 0/0 | 4740 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4735): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0038 | 0/0 | 4740 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4735): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0039 | 0/0 | 4741 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4736): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0040 | 0/0 | 4740 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4735): Show |
chr14 | 20281227 | 20310951 |
a0002c0004t0049 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
a0002c0010t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0003c0006t0013 | 0/0 | 4733 | 6 | 6 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4728): Show |
chr14 | 20281227 | 20310951 |
a0004c0005t0003 | 0/0 | 4738 | 5 | 5 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4733): Show |
chr14 | 20281227 | 20310951 |
a0004c0005t0020 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4729): Show |
chr14 | 20281227 | 20310951 |
a0005c0013t0001 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4730): Show |
chr14 | 20281227 | 20310951 |
a0006c0011t0002 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | GGAGT others(4734): Show |
chr14 | 20281227 | 20310951 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 53 | 0 | 6 | 43 | 2 | 2 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0002 | 0/0 | 19 | 7 | 5 | 4 | 0 | 3 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0006g0005 | 0/0 | 9 | 0 | 6 | 2 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0006g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0012g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0021g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0021g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0022g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0022g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0025g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0025g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0026g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0026g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0030g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0042g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0043g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0045g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0046g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0001t0047g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0004 | 0/0 | 15 | 0 | 5 | 9 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0008g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0008g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0009g0006 | 0/0 | 7 | 2 | 4 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0009g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0009g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0010g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0011g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0014g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0015g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0015g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0017g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0017g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0018g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0018g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0019g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0020g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0024g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0024g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0028g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0029g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0033g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0035g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0036g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0037g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0044g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0048g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0054g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0055g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0056g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0057g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0002t0058g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0007t0004g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0008t0014g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0009t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0009t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0001c0012t0027g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0003 | 1/0 | 19 | 0 | 1 | 13 | 1 | 3 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0012g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0016g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0016g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0018g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0018g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0023g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0023g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0031g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0032g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0034g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0041g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0050g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0051g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0052g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0003t0053g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0015 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0027g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0038g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0039g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0040g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0004t0049g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0002c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0003c0006t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0004c0005t0003g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0004c0005t0020g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0005c0013t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
a0006c0011t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00280 | hp2 | a0002 | c0003 | t0005 | g0003 | EUR | FIN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00323 | hp2 | a0001 | c0002 | t0003 | g0062 | EUR | FIN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00408 | hp2 | a0002 | c0004 | t0004 | g0041 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00438 | hp1 | a0001 | c0002 | t0035 | g0139 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00438 | hp2 | a0001 | c0002 | t0036 | g0132 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00735 | hp2 | a0002 | c0004 | t0039 | g0183 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00738 | hp2 | a0002 | c0004 | t0004 | g0160 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00741 | hp1 | a0002 | c0003 | t0018 | g0173 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01069 | hp2 | a0002 | c0004 | t0004 | g0040 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01070 | hp1 | a0001 | c0002 | t0009 | g0006 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01074 | hp2 | a0002 | c0004 | t0004 | g0181 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01081 | hp1 | a0001 | c0001 | t0026 | g0213 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01081 | hp2 | a0001 | c0002 | t0009 | g0006 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01099 | hp1 | a0001 | c0012 | t0027 | g0121 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01099 | hp2 | a0002 | c0004 | t0027 | g0172 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01109 | hp1 | a0001 | c0001 | t0022 | g0049 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0111 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01168 | hp1 | a0002 | c0003 | t0023 | g0174 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01168 | hp2 | a0001 | c0002 | t0009 | g0006 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01169 | hp1 | a0001 | c0002 | t0009 | g0006 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01175 | hp2 | a0002 | c0004 | t0004 | g0176 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0021 | AMR | PUR | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01255 | hp1 | a0002 | c0003 | t0007 | g0152 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01255 | hp2 | a0001 | c0002 | t0015 | g0024 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01256 | hp2 | a0001 | c0002 | t0015 | g0143 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01258 | hp2 | a0001 | c0002 | t0015 | g0024 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01261 | hp2 | a0001 | c0002 | t0014 | g0211 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01346 | hp2 | a0005 | c0013 | t0001 | g0102 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0070 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0108 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01361 | hp2 | a0002 | c0004 | t0004 | g0189 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01433 | hp1 | a0002 | c0003 | t0018 | g0170 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01496 | hp1 | a0002 | c0004 | t0004 | g0040 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01496 | hp2 | a0001 | c0002 | t0015 | g0024 | AMR | CLM | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01515 | hp2 | a0002 | c0003 | t0023 | g0043 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01516 | hp2 | a0001 | c0002 | t0009 | g0051 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01517 | hp2 | a0002 | c0003 | t0023 | g0043 | EUR | IBS | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01884 | hp1 | a0001 | c0001 | t0045 | g0107 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01884 | hp2 | a0002 | c0003 | t0007 | g0027 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0085 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01891 | hp2 | a0001 | c0002 | t0048 | g0063 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01934 | hp1 | a0002 | c0003 | t0005 | g0003 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01934 | hp2 | a0002 | c0004 | t0004 | g0016 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01952 | hp1 | a0001 | c0002 | t0018 | g0060 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0068 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02004 | hp2 | a0002 | c0004 | t0004 | g0015 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02015 | hp2 | a0002 | c0004 | t0049 | g0179 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02027 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0049 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02055 | hp2 | a0002 | c0003 | t0007 | g0027 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02074 | hp2 | a0002 | c0004 | t0004 | g0015 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02129 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02132 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02135 | hp1 | a0002 | c0004 | t0004 | g0090 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02145 | hp1 | a0001 | c0002 | t0008 | g0008 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02145 | hp2 | a0001 | c0008 | t0014 | g0018 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0106 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02155 | hp1 | a0002 | c0004 | t0004 | g0041 | EAS | CDX | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02165 | hp1 | a0002 | c0010 | t0001 | g0058 | EAS | CDX | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | CDX | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0209 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02258 | hp1 | a0001 | c0002 | t0011 | g0198 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02258 | hp2 | a0001 | c0002 | t0011 | g0017 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02280 | hp1 | a0001 | c0002 | t0011 | g0017 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02280 | hp2 | a0001 | c0002 | t0008 | g0008 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02293 | hp1 | a0001 | c0001 | t0047 | g0117 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0013 | AMR | PEL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02451 | hp2 | a0001 | c0002 | t0011 | g0196 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02523 | hp1 | a0002 | c0004 | t0004 | g0015 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0146 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02572 | hp2 | a0002 | c0003 | t0012 | g0204 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02602 | hp1 | a0002 | c0003 | t0007 | g0169 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02602 | hp2 | a0002 | c0004 | t0004 | g0015 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02615 | hp1 | a0001 | c0002 | t0011 | g0017 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02622 | hp1 | a0003 | c0006 | t0013 | g0202 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02622 | hp2 | a0001 | c0007 | t0004 | g0011 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02630 | hp1 | a0001 | c0001 | t0026 | g0212 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02630 | hp2 | a0003 | c0006 | t0013 | g0206 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02647 | hp1 | a0001 | c0002 | t0008 | g0208 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02647 | hp2 | a0001 | c0002 | t0011 | g0017 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0131 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02698 | hp2 | a0002 | c0003 | t0005 | g0164 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02717 | hp1 | a0003 | c0006 | t0013 | g0054 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02717 | hp2 | a0003 | c0006 | t0013 | g0200 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02735 | hp1 | a0002 | c0003 | t0050 | g0161 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02738 | hp1 | a0001 | c0001 | t0025 | g0215 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02738 | hp2 | a0002 | c0004 | t0040 | g0193 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02809 | hp1 | a0002 | c0004 | t0004 | g0185 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02809 | hp2 | a0001 | c0002 | t0020 | g0095 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02818 | hp1 | a0001 | c0002 | t0011 | g0199 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02886 | hp1 | a0001 | c0002 | t0028 | g0046 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02886 | hp2 | a0004 | c0005 | t0003 | g0010 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02895 | hp1 | a0004 | c0005 | t0003 | g0010 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02895 | hp2 | a0001 | c0002 | t0017 | g0080 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02896 | hp2 | a0004 | c0005 | t0020 | g0195 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02897 | hp2 | a0004 | c0005 | t0003 | g0010 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0048 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02922 | hp2 | a0001 | c0002 | t0018 | g0067 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02965 | hp1 | a0001 | c0007 | t0004 | g0011 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02965 | hp2 | a0002 | c0003 | t0041 | g0165 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02970 | hp1 | a0001 | c0002 | t0029 | g0047 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02976 | hp1 | a0001 | c0002 | t0028 | g0046 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02976 | hp2 | a0002 | c0003 | t0007 | g0039 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0029 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03041 | hp1 | a0002 | c0003 | t0012 | g0205 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03098 | hp1 | a0003 | c0006 | t0013 | g0201 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03098 | hp2 | a0001 | c0002 | t0014 | g0145 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03130 | hp1 | a0001 | c0002 | t0055 | g0197 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03139 | hp1 | a0001 | c0002 | t0008 | g0008 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0021 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03195 | hp1 | a0001 | c0002 | t0008 | g0008 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03195 | hp2 | a0002 | c0003 | t0007 | g0153 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03209 | hp1 | a0001 | c0002 | t0017 | g0084 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0142 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03225 | hp2 | a0002 | c0003 | t0007 | g0159 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03239 | hp2 | a0002 | c0004 | t0004 | g0088 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03453 | hp1 | a0001 | c0008 | t0014 | g0018 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03453 | hp2 | a0001 | c0002 | t0056 | g0207 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03486 | hp1 | a0001 | c0002 | t0020 | g0094 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03486 | hp2 | a0001 | c0007 | t0004 | g0011 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03490 | hp1 | a0002 | c0004 | t0004 | g0184 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03491 | hp2 | a0002 | c0003 | t0005 | g0003 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03492 | hp2 | a0002 | c0003 | t0005 | g0003 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03516 | hp1 | a0003 | c0006 | t0013 | g0053 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0021 | AFR | ESN | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03540 | hp1 | a0001 | c0002 | t0017 | g0064 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03540 | hp2 | a0001 | c0002 | t0017 | g0083 | AFR | GWD | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03579 | hp1 | a0002 | c0003 | t0007 | g0027 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03579 | hp2 | a0001 | c0002 | t0006 | g0087 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03654 | hp1 | a0002 | c0003 | t0005 | g0003 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03669 | hp2 | a0002 | c0003 | t0005 | g0158 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03688 | hp1 | a0002 | c0003 | t0034 | g0168 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03710 | hp1 | a0002 | c0003 | t0053 | g0163 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0029 | SAS | PJL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03831 | hp2 | a0001 | c0001 | t0030 | g0114 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0005 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03927 | hp2 | a0002 | c0003 | t0005 | g0026 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04115 | hp2 | a0002 | c0004 | t0004 | g0044 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04184 | hp1 | a0002 | c0004 | t0004 | g0188 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04184 | hp2 | a0002 | c0003 | t0005 | g0026 | SAS | BEB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0079 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0037 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04204 | hp1 | a0002 | c0003 | t0007 | g0167 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04228 | hp1 | a0002 | c0004 | t0004 | g0175 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG04228 | hp2 | a0002 | c0004 | t0004 | g0089 | SAS | STU | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18522 | hp1 | a0001 | c0002 | t0008 | g0008 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18522 | hp2 | a0001 | c0002 | t0057 | g0073 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | CHB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0186 | EAS | CHB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0178 | EAS | CHB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | CHB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18906 | hp1 | a0001 | c0002 | t0058 | g0218 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18906 | hp2 | a0001 | c0008 | t0014 | g0018 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18940 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18945 | hp1 | a0002 | c0004 | t0004 | g0016 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18946 | hp1 | a0002 | c0004 | t0004 | g0016 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18947 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18949 | hp2 | a0002 | c0004 | t0004 | g0180 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18953 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18961 | hp2 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18963 | hp2 | a0002 | c0003 | t0016 | g0192 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18964 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18966 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18968 | hp1 | a0002 | c0003 | t0016 | g0187 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18969 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18970 | hp1 | a0001 | c0002 | t0019 | g0019 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18970 | hp2 | a0002 | c0003 | t0016 | g0042 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18972 | hp1 | a0001 | c0002 | t0019 | g0019 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18975 | hp1 | a0006 | c0011 | t0002 | g0194 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18977 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18978 | hp2 | a0002 | c0004 | t0004 | g0045 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18979 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18982 | hp1 | a0002 | c0003 | t0052 | g0162 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18983 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18983 | hp2 | a0002 | c0003 | t0003 | g0157 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18986 | hp2 | a0002 | c0003 | t0051 | g0182 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18987 | hp1 | a0001 | c0001 | t0043 | g0098 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18988 | hp1 | a0001 | c0001 | t0025 | g0115 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18988 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18990 | hp1 | a0001 | c0001 | t0042 | g0123 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18991 | hp2 | a0002 | c0003 | t0031 | g0154 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18992 | hp2 | a0001 | c0002 | t0037 | g0133 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18994 | hp1 | a0001 | c0002 | t0019 | g0019 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18995 | hp1 | a0002 | c0003 | t0032 | g0171 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18998 | hp1 | a0002 | c0004 | t0004 | g0044 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18999 | hp1 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18999 | hp2 | a0001 | c0001 | t0021 | g0032 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19000 | hp1 | a0002 | c0003 | t0005 | g0026 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19001 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19009 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0155 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19011 | hp2 | a0002 | c0003 | t0016 | g0042 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19030 | hp1 | a0001 | c0002 | t0054 | g0203 | AFR | LWK | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0008 | AFR | LWK | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19057 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19058 | hp1 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19059 | hp2 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19060 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19063 | hp2 | a0001 | c0001 | t0046 | g0116 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19064 | hp2 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19066 | hp1 | a0002 | c0004 | t0038 | g0191 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19070 | hp1 | a0001 | c0002 | t0010 | g0050 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19074 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19074 | hp2 | a0001 | c0001 | t0021 | g0032 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19075 | hp2 | a0002 | c0003 | t0005 | g0177 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19076 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19076 | hp2 | a0002 | c0004 | t0004 | g0092 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19077 | hp1 | a0001 | c0009 | t0002 | g0130 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19078 | hp2 | a0002 | c0004 | t0004 | g0045 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19080 | hp1 | a0002 | c0004 | t0004 | g0016 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19081 | hp1 | a0002 | c0003 | t0005 | g0156 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19084 | hp2 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19085 | hp2 | a0001 | c0002 | t0033 | g0086 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19087 | hp1 | a0001 | c0009 | t0002 | g0129 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19087 | hp2 | a0001 | c0001 | t0021 | g0097 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19089 | hp1 | a0001 | c0002 | t0010 | g0007 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19090 | hp1 | a0001 | c0002 | t0010 | g0065 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19090 | hp2 | a0002 | c0003 | t0005 | g0003 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19091 | hp1 | a0001 | c0002 | t0024 | g0074 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19091 | hp2 | a0001 | c0002 | t0024 | g0072 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19240 | hp1 | a0001 | c0007 | t0004 | g0011 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0048 | AFR | YRI | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20129 | hp1 | a0004 | c0005 | t0003 | g0010 | AFR | ASW | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20129 | hp2 | a0001 | c0002 | t0009 | g0006 | AFR | ASW | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20905 | hp2 | a0001 | c0002 | t0009 | g0006 | SAS | GIH | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0103 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02486 | hp2 | a0001 | c0007 | t0004 | g0011 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02559 | hp1 | a0002 | c0003 | t0007 | g0166 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03471 | hp1 | a0001 | c0002 | t0029 | g0047 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG06807 | hp1 | a0004 | c0005 | t0003 | g0010 | AFR | USA | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
HG06807 | hp2 | a0002 | c0003 | t0007 | g0039 | AFR | USA | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA20300 | hp2 | a0001 | c0002 | t0044 | g0096 | AFR | USA | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0214 | AFR | LWK | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
NA21309 | hp2 | a0001 | c0002 | t0009 | g0006 | AFR | LWK | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
homoSapiens | chm13v2 | a0001 | c0002 | t0009 | g0052 | REF | REF | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
homoSapiens | grch38p0 | a0002 | c0003 | t0005 | g0003 | REF | REF | TTC5_chr14_20281227_20310951 | TTC5 | chr14 | 20281227 | 20310951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:20289679 | C | A | 1 | a0003 | 6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
missense_variant | MODERATE | c.1271G>T | p.Gly424Val | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1285/4737 | 1271/1323 | 424/440 | chr14 | 20289679 | |||
chr14:20292126 | T | C | 1 | a0005 | 1 | HG01346.hp2 | missense_variant&splice_region_variant | MODERATE | c.1060A>G | p.Thr354Ala | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/10 | 1074/4737 | 1060/1323 | 354/440 | chr14 | 20292126 | |||
chr14:20295364 | C | T | 1 | a0004 | 6 | HG02886.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
missense_variant | MODERATE | c.1006G>A | p.Val336Ile | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/10 | 1020/4737 | 1006/1323 | 336/440 | chr14 | 20295364 | |||
chr14:20300679 | C | A | 1 | a0006 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.324G>T | p.Gln108His | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/10 | 338/4737 | 324/1323 | 108/440 | chr14 | 20300679 | |||
chr14:20300680 | T | A | 1 | a0006 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.323A>T | p.Gln108Leu | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/10 | 337/4737 | 323/1323 | 108/440 | chr14 | 20300680 | |||
chr14:20301877 | T | C | 3 | a0001 a0003 a0005 |
312 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(309): Show |
missense_variant | MODERATE | c.140A>G | p.Gln47Arg | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/10 | 154/4737 | 140/1323 | 47/440 | chr14 | 20301877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:20289645 | C | A | 3 | a0001c0007 a0001c0012 a0002c0004 |
40 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.1305G>T | p.Ser435Ser | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1319/4737 | 1305/1323 | 435/440 | chr14 | 20289645 | |||
chr14:20295344 | T | C | 1 | a0001c0008 | 3 | HG02145.hp2 HG03453.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.1026A>G | p.Val342Val | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/10 | 1040/4737 | 1026/1323 | 342/440 | chr14 | 20295344 | |||
chr14:20296426 | A | C | 4 | a0001c0001 a0001c0012 a0002c0010 others(1): Show |
153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
synonymous_variant | LOW | c.660T>G | p.Ala220Ala | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/10 | 674/4737 | 660/1323 | 220/440 | chr14 | 20296426 | |||
chr14:20301951 | C | T | 1 | a0001c0009 | 2 | NA19077.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.66G>A | p.Gln22Gln | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/10 | 80/4737 | 66/1323 | 22/440 | chr14 | 20301951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:20286243 | A | G | 1 | a0002c0003t0052 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3384T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3384 | chr14 | 20286243 | ||||||
chr14:20286295 | T | C | 1 | a0002c0003t0032 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3332A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3332 | chr14 | 20286295 | ||||||
chr14:20286355 | G | C | 9 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0019 others(6): Show |
47 | HG00323.hp2 HG00544.hp1 HG01070.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3272C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3272 | chr14 | 20286355 | ||||||
chr14:20286465 | G | A | 1 | a0001c0002t0019 | 3 | NA18970.hp1 NA18972.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3162C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3162 | chr14 | 20286465 | ||||||
chr14:20286526 | T | G | 1 | a0001c0002t0008 | 10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3101A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3101 | chr14 | 20286526 | ||||||
chr14:20286553 | G | A | 16 | a0001c0001t0002 a0001c0001t0021 a0001c0002t0002 others(13): Show |
83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3074C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3074 | chr14 | 20286553 | ||||||
chr14:20286611 | A | G | 1 | a0001c0002t0029 | 2 | HG02970.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3016T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 3016 | chr14 | 20286611 | ||||||
chr14:20286746 | T | TA | 29 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(26): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2880dupT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2880 | chr14 | 20286746 | ||||||
chr14:20286841 | C | G | 1 | a0001c0002t0054 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2786 | chr14 | 20286841 | ||||||
chr14:20286976 | C | T | 1 | a0002c0003t0032 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2651G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2651 | chr14 | 20286976 | ||||||
chr14:20287124 | A | G | 1 | a0001c0001t0021 | 3 | NA18999.hp2 NA19074.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2503T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2503 | chr14 | 20287124 | ||||||
chr14:20287128 | C | A | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(20): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*2499G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2499 | chr14 | 20287128 | ||||||
chr14:20287183 | G | A | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(59): Show |
334 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*2444C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2444 | chr14 | 20287183 | ||||||
chr14:20287197 | T | C | 2 | a0001c0001t0022 a0001c0001t0026 |
5 | HG01081.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2430A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2430 | chr14 | 20287197 | ||||||
chr14:20287203 | AAC | A | 2 | a0001c0001t0022 a0001c0001t0026 |
5 | HG01081.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2423delGT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2422 | chr14 | 20287203 | ||||||
chr14:20287213 | G | C | 1 | a0001c0001t0046 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2414C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2414 | chr14 | 20287213 | ||||||
chr14:20287222 | C | T | 42 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(39): Show |
235 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*2405G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2405 | chr14 | 20287222 | ||||||
chr14:20287365 | A | G | 1 | a0002c0003t0051 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2262T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2262 | chr14 | 20287365 | ||||||
chr14:20287385 | A | C | 1 | a0001c0001t0026 | 2 | HG01081.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2242T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2242 | chr14 | 20287385 | ||||||
chr14:20287411 | T | TA | 1 | a0001c0002t0008 | 10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2215dupT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2215 | chr14 | 20287411 | ||||||
chr14:20287449 | A | G | 1 | a0001c0002t0028 | 2 | HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2178T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2178 | chr14 | 20287449 | ||||||
chr14:20287464 | T | C | 10 | a0001c0001t0002 a0001c0001t0021 a0001c0002t0002 others(7): Show |
67 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2163A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2163 | chr14 | 20287464 | ||||||
chr14:20287528 | T | C | 3 | a0001c0001t0012 a0001c0001t0045 a0002c0003t0012 |
7 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2099A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2099 | chr14 | 20287528 | ||||||
chr14:20287552 | G | T | 1 | a0001c0001t0045 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2075C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2075 | chr14 | 20287552 | ||||||
chr14:20287565 | T | C | 1 | a0001c0002t0017 | 4 | HG02895.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2062A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 2062 | chr14 | 20287565 | ||||||
chr14:20287631 | A | G | 1 | a0001c0002t0009 | 8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1996T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1996 | chr14 | 20287631 | ||||||
chr14:20287647 | G | A | 4 | a0001c0002t0014 a0001c0002t0017 a0001c0002t0054 others(1): Show |
10 | HG01261.hp2 HG02145.hp2 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1980C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1980 | chr14 | 20287647 | ||||||
chr14:20287734 | G | A | 1 | a0001c0002t0017 | 4 | HG02895.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1893C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1893 | chr14 | 20287734 | ||||||
chr14:20287765 | C | T | 1 | a0001c0002t0044 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1862G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1862 | chr14 | 20287765 | ||||||
chr14:20287847 | C | A | 1 | a0002c0004t0040 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1780 | chr14 | 20287847 | ||||||
chr14:20288118 | C | G | 8 | a0001c0002t0014 a0001c0002t0017 a0001c0002t0018 others(5): Show |
18 | HG00741.hp1 HG01168.hp1 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1509G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1509 | chr14 | 20288118 | ||||||
chr14:20288182 | C | CAGAT | 3 | a0001c0002t0015 a0002c0003t0016 a0002c0003t0051 |
9 | HG01255.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1444dupATCT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1444 | chr14 | 20288182 | ||||||
chr14:20288182 | CAGAT | C | 20 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(17): Show |
156 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1444delATCT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1441 | chr14 | 20288182 | ||||||
chr14:20288198 | T | C | 4 | a0001c0002t0014 a0001c0002t0017 a0001c0002t0054 others(1): Show |
10 | HG01261.hp2 HG02145.hp2 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1429A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1429 | chr14 | 20288198 | ||||||
chr14:20288202 | T | C | 1 | a0001c0002t0036 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1425A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1425 | chr14 | 20288202 | ||||||
chr14:20288206 | CAGAT | C | 1 | a0001c0002t0009 | 8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1417_*1420delATCT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1417 | chr14 | 20288206 | ||||||
chr14:20288246 | C | A | 1 | a0001c0002t0037 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1381G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1381 | chr14 | 20288246 | ||||||
chr14:20288246 | C | T | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(44): Show |
279 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1381G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1381 | chr14 | 20288246 | ||||||
chr14:20288262 | G | A | 8 | a0001c0002t0014 a0001c0002t0017 a0001c0002t0018 others(5): Show |
18 | HG00741.hp1 HG01168.hp1 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1365C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1365 | chr14 | 20288262 | ||||||
chr14:20288267 | C | A | 1 | a0001c0001t0047 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1360G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1360 | chr14 | 20288267 | ||||||
chr14:20288338 | G | T | 1 | a0001c0002t0057 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1289 | chr14 | 20288338 | ||||||
chr14:20288348 | C | T | 1 | a0002c0003t0050 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1279 | chr14 | 20288348 | ||||||
chr14:20288391 | G | A | 9 | a0001c0001t0002 a0001c0001t0021 a0001c0002t0002 others(6): Show |
59 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1236C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1236 | chr14 | 20288391 | ||||||
chr14:20288456 | G | A | 1 | a0001c0002t0048 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1171C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1171 | chr14 | 20288456 | ||||||
chr14:20288462 | G | A | 1 | a0001c0001t0022 | 3 | HG01109.hp1 HG02055.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1165C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1165 | chr14 | 20288462 | ||||||
chr14:20288604 | C | T | 1 | a0001c0001t0043 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1023G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1023 | chr14 | 20288604 | ||||||
chr14:20288623 | C | T | 1 | a0001c0001t0042 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1004G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 1004 | chr14 | 20288623 | ||||||
chr14:20288628 | C | T | 1 | a0002c0003t0041 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 999 | chr14 | 20288628 | ||||||
chr14:20288728 | T | C | 14 | a0001c0001t0011 a0001c0002t0004 a0001c0002t0011 others(11): Show |
54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*899A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 899 | chr14 | 20288728 | ||||||
chr14:20288735 | C | T | 1 | a0002c0004t0049 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 892 | chr14 | 20288735 | ||||||
chr14:20289026 | C | T | 2 | a0001c0002t0020 a0004c0005t0020 |
3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*601G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 601 | chr14 | 20289026 | ||||||
chr14:20289037 | G | GA | 14 | a0001c0001t0011 a0001c0002t0004 a0001c0002t0011 others(11): Show |
54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*589dupT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 589 | chr14 | 20289037 | ||||||
chr14:20289130 | G | GT | 36 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(33): Show |
243 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*496dupA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 496 | chr14 | 20289130 | ||||||
chr14:20289130 | G | GTT | 16 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0025 others(13): Show |
74 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*495_*496dupAA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 496 | chr14 | 20289130 | ||||||
chr14:20289224 | A | G | 12 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0010 others(9): Show |
58 | HG00323.hp2 HG00544.hp1 HG01070.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*403T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 403 | chr14 | 20289224 | ||||||
chr14:20289233 | A | G | 1 | a0001c0001t0030 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 394 | chr14 | 20289233 | ||||||
chr14:20289263 | T | G | 1 | a0002c0003t0023 | 3 | HG01168.hp1 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*364A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 364 | chr14 | 20289263 | ||||||
chr14:20289288 | T | G | 1 | a0001c0002t0056 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*339A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 339 | chr14 | 20289288 | ||||||
chr14:20289359 | C | T | 1 | a0001c0002t0009 | 8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*268G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 268 | chr14 | 20289359 | ||||||
chr14:20289374 | T | C | 1 | a0001c0002t0029 | 2 | HG02970.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*253A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 253 | chr14 | 20289374 | ||||||
chr14:20289569 | G | A | 4 | a0001c0002t0018 a0001c0002t0057 a0002c0003t0018 others(1): Show |
8 | HG00741.hp1 HG01168.hp1 HG01433.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*58C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 10/10 | 58 | chr14 | 20289569 | ||||||
chr14:20305943 | G | A | 1 | a0001c0002t0058 | 1 | NA18906.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/10 | chr14 | 20305943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:20289951 | A | C | 2 | a0001c0002t0017g0083 a0001c0002t0017g0084 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1204-205T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20289951 | |||||||
chr14:20289954 | T | C | 1 | a0002c0003t0005g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1204-208A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20289954 | |||||||
chr14:20290046 | C | G | 2 | a0001c0002t0020g0094 a0001c0002t0020g0095 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1204-300G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290046 | |||||||
chr14:20290156 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1204-410T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290156 | |||||||
chr14:20290207 | A | C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(1): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1204-461T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290207 | |||||||
chr14:20290267 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(203): Show |
383 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(380): Show |
intron_variant | MODIFIER | c.1204-521T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290267 | |||||||
chr14:20290282 | G | C | 1 | a0001c0002t0048g0063 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1204-536C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290282 | |||||||
chr14:20290295 | T | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(144): Show |
304 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1204-549A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290295 | |||||||
chr14:20290319 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1204-573A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290319 | |||||||
chr14:20290323 | T | C | 4 | a0001c0002t0044g0096 a0002c0003t0007g0166 a0002c0003t0012g0204 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-577A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290323 | |||||||
chr14:20290345 | G | A | 44 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(41): Show |
70 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.1204-599C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290345 | |||||||
chr14:20290434 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(144): Show |
304 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1204-688T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290434 | |||||||
chr14:20290583 | T | C | 2 | a0001c0002t0006g0142 a0001c0002t0006g0146 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1204-837A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290583 | |||||||
chr14:20290714 | T | C | 1 | a0001c0007t0004g0011 | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-968A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290714 | |||||||
chr14:20290790 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(144): Show |
304 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1204-1044C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20290790 | |||||||
chr14:20291011 | G | A | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203+972C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291011 | |||||||
chr14:20291012 | C | A | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203+971G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291012 | |||||||
chr14:20291033 | TAAC | T | 3 | a0001c0002t0003g0028 a0001c0002t0003g0055 a0001c0002t0003g0057 |
4 | HG02027.hp1 NA18747.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203+947_1203+949d others(5): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291033 | |||||||
chr14:20291054 | CTT | C | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203+927_1203+928d others(4): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291054 | |||||||
chr14:20291392 | C | T | 2 | a0004c0005t0003g0010 a0004c0005t0020g0195 |
6 | HG02886.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+591G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291392 | |||||||
chr14:20291538 | T | C | 1 | a0002c0004t0004g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1203+445A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291538 | |||||||
chr14:20291539 | G | C | 1 | a0002c0004t0004g0181 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1203+444C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291539 | |||||||
chr14:20291711 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1203+272A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291711 | |||||||
chr14:20291723 | T | C | 2 | a0001c0002t0006g0142 a0001c0002t0006g0146 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1203+260A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291723 | |||||||
chr14:20291846 | CATATACA others(7): Show |
C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(1): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1203+123_1203+136d others(16): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291846 | |||||||
chr14:20291907 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(51): Show |
151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1203+76A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291907 | |||||||
chr14:20291952 | G | A | 1 | a0005c0013t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1203+31C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 9/9 | chr14 | 20291952 | |||||||
chr14:20292190 | G | A | 37 | a0001c0002t0014g0211 a0001c0007t0004g0011 a0002c0003t0001g0178 others(34): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1059-63C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292190 | |||||||
chr14:20292191 | C | A | 37 | a0001c0002t0014g0211 a0001c0007t0004g0011 a0002c0003t0001g0178 others(34): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1059-64G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292191 | |||||||
chr14:20292227 | G | T | 2 | a0002c0003t0007g0169 a0002c0003t0034g0168 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1059-100C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292227 | |||||||
chr14:20292239 | G | C | 6 | a0001c0002t0011g0017 a0001c0002t0011g0196 a0001c0002t0011g0198 others(3): Show |
10 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-112C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292239 | |||||||
chr14:20292245 | G | A | 1 | a0001c0002t0002g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1059-118C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292245 | |||||||
chr14:20292273 | CTTAA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(51): Show |
151 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1059-150_1059-147d others(6): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292273 | |||||||
chr14:20292307 | A | G | 1 | a0001c0002t0003g0135 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1059-180T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292307 | |||||||
chr14:20292409 | T | C | 1 | a0002c0003t0007g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1059-282A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292409 | |||||||
chr14:20292427 | A | C | 3 | a0002c0004t0004g0160 a0002c0004t0004g0181 a0002c0004t0027g0172 |
3 | HG00738.hp2 HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1059-300T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292427 | |||||||
chr14:20292474 | A | C | 2 | a0003c0006t0013g0200 a0003c0006t0013g0201 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1059-347T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292474 | |||||||
chr14:20292512 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1059-385A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292512 | |||||||
chr14:20292514 | A | C | 1 | a0001c0002t0058g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1059-387T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292514 | |||||||
chr14:20292714 | G | A | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059-587C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292714 | |||||||
chr14:20292747 | A | G | 2 | a0001c0002t0006g0142 a0001c0002t0006g0146 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1059-620T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292747 | |||||||
chr14:20292912 | G | T | 1 | a0003c0006t0013g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059-785C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292912 | |||||||
chr14:20292979 | T | C | 1 | a0001c0002t0011g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1059-852A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20292979 | |||||||
chr14:20293116 | T | C | 4 | a0001c0002t0006g0142 a0001c0002t0006g0146 a0001c0002t0020g0094 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-989A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293116 | |||||||
chr14:20293183 | G | A | 1 | a0002c0004t0004g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1059-1056C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293183 | |||||||
chr14:20293338 | G | A | 2 | a0002c0003t0007g0169 a0002c0003t0034g0168 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1059-1211C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293338 | |||||||
chr14:20293444 | TGGGAAAG others(30): Show |
T | 1 | a0002c0003t0005g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1059-1354_1059-131 others(41): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293444 | |||||||
chr14:20293457 | A | G | 93 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(90): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1059-1330T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293457 | |||||||
chr14:20293481 | G | A | 1 | a0001c0008t0014g0018 | 3 | HG02145.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1059-1354C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293481 | |||||||
chr14:20293682 | G | C | 1 | a0001c0001t0012g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1059-1555C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293682 | |||||||
chr14:20293857 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1058+1455C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293857 | |||||||
chr14:20293876 | C | T | 5 | a0001c0002t0003g0068 a0001c0002t0003g0070 a0001c0002t0003g0075 others(2): Show |
5 | HG01358.hp2 HG01433.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+1436G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293876 | |||||||
chr14:20293907 | A | G | 93 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(90): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1058+1405T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20293907 | |||||||
chr14:20294052 | C | T | 1 | a0002c0004t0004g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1058+1260G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294052 | |||||||
chr14:20294112 | C | T | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1058+1200G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294112 | |||||||
chr14:20294444 | C | T | 1 | a0002c0003t0052g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1058+868G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294444 | |||||||
chr14:20294459 | T | C | 1 | a0003c0006t0013g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1058+853A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294459 | |||||||
chr14:20294616 | G | T | 93 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(90): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1058+696C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294616 | |||||||
chr14:20294847 | A | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(48): Show |
147 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1058+465T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20294847 | |||||||
chr14:20295002 | A | T | 30 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(27): Show |
53 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1058+310T>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20295002 | |||||||
chr14:20295031 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1058+281T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20295031 | |||||||
chr14:20295229 | C | G | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1058+83G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20295229 | |||||||
chr14:20295287 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(203): Show |
383 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(380): Show |
intron_variant | MODIFIER | c.1058+25A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 8/9 | chr14 | 20295287 | |||||||
chr14:20295557 | G | A | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-31C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 7/9 | chr14 | 20295557 | |||||||
chr14:20295872 | C | T | 36 | a0001c0007t0004g0011 a0002c0003t0001g0178 a0002c0003t0001g0186 others(33): Show |
52 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.697-18G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/9 | chr14 | 20295872 | |||||||
chr14:20295935 | G | C | 36 | a0001c0007t0004g0011 a0002c0003t0001g0178 a0002c0003t0001g0186 others(33): Show |
52 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.697-81C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/9 | chr14 | 20295935 | |||||||
chr14:20295971 | G | A | 3 | a0002c0003t0007g0167 a0002c0003t0007g0169 a0002c0003t0034g0168 |
3 | HG02602.hp1 HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.697-117C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/9 | chr14 | 20295971 | |||||||
chr14:20295998 | G | C | 3 | a0001c0002t0002g0023 a0001c0002t0002g0036 a0001c0002t0002g0099 |
6 | HG02165.hp2 NA18966.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-144C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/9 | chr14 | 20295998 | |||||||
chr14:20296197 | C | A | 1 | a0001c0002t0017g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.696+193G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 6/9 | chr14 | 20296197 | |||||||
chr14:20296480 | T | C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(1): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.640-34A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296480 | |||||||
chr14:20296503 | T | C | 1 | a0002c0003t0003g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.640-57A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296503 | |||||||
chr14:20296586 | T | C | 2 | a0001c0002t0020g0094 a0001c0002t0020g0095 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.640-140A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296586 | |||||||
chr14:20296601 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.640-155C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296601 | |||||||
chr14:20296605 | A | G | 2 | a0001c0001t0022g0049 a0001c0001t0022g0214 |
3 | HG01109.hp1 HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.640-159T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296605 | |||||||
chr14:20296625 | T | G | 4 | a0001c0001t0022g0049 a0001c0001t0022g0214 a0001c0001t0026g0212 others(1): Show |
5 | HG01081.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-179A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296625 | |||||||
chr14:20296635 | A | C | 1 | a0001c0007t0004g0011 | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-189T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296635 | |||||||
chr14:20296647 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(52): Show |
153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.640-201A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296647 | |||||||
chr14:20296727 | T | C | 3 | a0001c0002t0017g0080 a0001c0002t0017g0083 a0001c0002t0017g0084 |
3 | HG02895.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.640-281A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296727 | |||||||
chr14:20296761 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.640-315G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296761 | |||||||
chr14:20296855 | A | C | 1 | a0001c0002t0011g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640-409T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296855 | |||||||
chr14:20296869 | T | C | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.640-423A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296869 | |||||||
chr14:20296964 | T | C | 94 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(91): Show |
154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.640-518A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20296964 | |||||||
chr14:20297299 | G | C | 1 | a0001c0012t0027g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640-853C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297299 | |||||||
chr14:20297537 | G | A | 2 | a0001c0001t0022g0049 a0001c0001t0022g0214 |
3 | HG01109.hp1 HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.640-1091C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297537 | |||||||
chr14:20297602 | C | G | 2 | a0001c0001t0022g0049 a0001c0001t0022g0214 |
3 | HG01109.hp1 HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.640-1156G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297602 | |||||||
chr14:20297638 | T | C | 48 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(45): Show |
74 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.639+1159A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297638 | |||||||
chr14:20297728 | G | A | 2 | a0004c0005t0003g0010 a0004c0005t0020g0195 |
6 | HG02886.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+1069C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297728 | |||||||
chr14:20297766 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.639+1031G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297766 | |||||||
chr14:20297804 | T | C | 1 | a0001c0002t0011g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.639+993A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297804 | |||||||
chr14:20297826 | G | T | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+971C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297826 | |||||||
chr14:20297859 | G | A | 1 | a0002c0003t0007g0039 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.639+938C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297859 | |||||||
chr14:20297985 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(149): Show |
310 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.639+812G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20297985 | |||||||
chr14:20298067 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.639+730C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298067 | |||||||
chr14:20298108 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.639+689G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298108 | |||||||
chr14:20298308 | T | C | 48 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(45): Show |
76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.639+489A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298308 | |||||||
chr14:20298335 | A | G | 1 | a0001c0002t0002g0038 | 2 | NA18954.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.639+462T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298335 | |||||||
chr14:20298459 | A | C | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.639+338T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298459 | |||||||
chr14:20298514 | T | C | 1 | a0002c0003t0005g0156 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.639+283A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298514 | |||||||
chr14:20298559 | C | CCAGACAG others(30): Show |
1 | a0002c0003t0005g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.639+201_639+237dup others(37): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298559 | |||||||
chr14:20298608 | GT | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0022 others(27): Show |
101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.639+188delA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298608 | |||||||
chr14:20298615 | A | C | 2 | a0002c0003t0005g0158 a0002c0003t0050g0161 |
2 | HG02735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.639+182T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298615 | |||||||
chr14:20298633 | G | A | 2 | a0004c0005t0003g0010 a0004c0005t0020g0195 |
6 | HG02886.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+164C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298633 | |||||||
chr14:20298639 | C | A | 1 | a0001c0002t0024g0074 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.639+158G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298639 | |||||||
chr14:20298670 | A | C | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.639+127T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 5/9 | chr14 | 20298670 | |||||||
chr14:20298950 | G | C | 1 | a0001c0002t0002g0036 | 2 | HG02165.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.548-62C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 4/9 | chr14 | 20298950 | |||||||
chr14:20298961 | A | G | 1 | a0001c0002t0003g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.548-73T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 4/9 | chr14 | 20298961 | |||||||
chr14:20298980 | C | T | 1 | a0004c0005t0020g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.548-92G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 4/9 | chr14 | 20298980 | |||||||
chr14:20299009 | G | A | 2 | a0001c0001t0022g0049 a0001c0001t0022g0214 |
3 | HG01109.hp1 HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.548-121C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 4/9 | chr14 | 20299009 | |||||||
chr14:20299459 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(151): Show |
313 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(310): Show |
intron_variant | MODIFIER | c.397-11C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299459 | |||||||
chr14:20299547 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(135): Show |
282 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.397-99G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299547 | |||||||
chr14:20299559 | T | C | 2 | a0001c0002t0002g0140 a0001c0002t0035g0139 |
2 | HG00438.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.397-111A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299559 | |||||||
chr14:20299577 | G | A | 1 | a0001c0002t0002g0136 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.397-129C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299577 | |||||||
chr14:20299647 | G | A | 3 | a0001c0002t0003g0070 a0001c0002t0003g0075 a0001c0002t0003g0078 |
3 | HG01358.hp2 HG01433.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.397-199C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299647 | |||||||
chr14:20299709 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(52): Show |
153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.397-261A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299709 | |||||||
chr14:20299713 | C | T | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.397-265G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299713 | |||||||
chr14:20299804 | CA | C | 2 | a0001c0002t0002g0037 a0001c0002t0002g0137 |
3 | HG03927.hp1 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.397-357delT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20299804 | |||||||
chr14:20300021 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.397-573C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300021 | |||||||
chr14:20300131 | C | T | 34 | a0001c0001t0001g0076 a0001c0002t0001g0056 a0001c0002t0003g0012 others(31): Show |
49 | HG00323.hp2 HG00544.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.396+476G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300131 | |||||||
chr14:20300143 | G | GTATATAT others(3): Show |
2 | a0002c0003t0001g0178 a0002c0004t0049g0179 |
2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.396+454_396+463dup others(10): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(5): Show |
3 | a0001c0002t0008g0008 a0001c0002t0008g0208 a0002c0004t0004g0180 |
8 | HG02145.hp1 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.396+452_396+463dup others(12): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(7): Show |
5 | a0001c0002t0011g0017 a0001c0002t0011g0198 a0001c0002t0028g0046 others(2): Show |
10 | HG00408.hp2 HG02155.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(14): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(9): Show |
1 | a0001c0002t0008g0048 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.396+463_396+464ins others(16): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(11): Show |
1 | a0001c0002t0008g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(18): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(13): Show |
1 | a0001c0002t0029g0047 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.396+463_396+464ins others(20): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(19): Show |
11 | a0002c0003t0016g0042 a0002c0003t0018g0173 a0002c0003t0023g0043 others(8): Show |
13 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(26): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(21): Show |
5 | a0002c0003t0001g0186 a0002c0003t0016g0187 a0002c0004t0004g0015 others(2): Show |
8 | HG02004.hp2 HG02074.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(28): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(23): Show |
4 | a0002c0004t0004g0176 a0002c0004t0004g0188 a0002c0004t0004g0189 others(1): Show |
4 | HG01175.hp2 HG01361.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(30): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(25): Show |
1 | a0002c0004t0004g0044 | 2 | HG04115.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.396+463_396+464ins others(32): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(29): Show |
2 | a0002c0004t0004g0045 a0002c0004t0004g0092 |
3 | NA18978.hp2 NA19076.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.396+463_396+464ins others(36): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(31): Show |
1 | a0002c0003t0001g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(38): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATATAT others(35): Show |
1 | a0002c0004t0038g0191 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(42): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(5): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(35): Show |
129 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(12): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(7): Show |
10 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0034 others(7): Show |
16 | HG01081.hp1 HG01099.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(14): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(9): Show |
5 | a0001c0001t0001g0124 a0001c0001t0022g0049 a0001c0001t0022g0214 others(2): Show |
6 | HG00735.hp1 HG01109.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(16): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(11): Show |
2 | a0001c0001t0001g0100 a0001c0002t0058g0218 |
2 | HG00280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.396+463_396+464ins others(18): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(13): Show |
1 | a0001c0002t0054g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(20): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(17): Show |
2 | a0001c0002t0048g0063 a0001c0008t0014g0018 |
4 | HG01891.hp2 HG02145.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(24): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(19): Show |
2 | a0001c0002t0017g0064 a0001c0002t0018g0067 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.396+463_396+464ins others(26): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(21): Show |
8 | a0001c0002t0003g0013 a0001c0002t0003g0055 a0001c0002t0003g0057 others(5): Show |
11 | HG01358.hp2 HG01891.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(28): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(23): Show |
12 | a0001c0001t0001g0076 a0001c0002t0003g0028 a0001c0002t0003g0062 others(9): Show |
20 | HG00323.hp2 HG01433.hp2 NA18522.hp2 others(17): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(30): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(25): Show |
6 | a0001c0002t0003g0066 a0001c0002t0003g0077 a0001c0002t0003g0078 others(3): Show |
6 | HG01952.hp1 HG01978.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(32): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(27): Show |
3 | a0001c0002t0003g0029 a0001c0002t0003g0059 a0001c0002t0003g0079 |
4 | HG03017.hp2 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(34): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(29): Show |
1 | a0001c0002t0017g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(36): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(31): Show |
1 | a0001c0002t0003g0082 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(38): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(35): Show |
1 | a0001c0002t0017g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(42): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(37): Show |
1 | a0001c0002t0017g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(44): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTATGTGT others(9): Show |
1 | a0001c0001t0026g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(16): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(13): Show |
23 | a0001c0002t0002g0004 a0001c0002t0002g0023 a0001c0002t0002g0036 others(20): Show |
44 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(20): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(15): Show |
5 | a0001c0002t0001g0138 a0001c0002t0002g0025 a0001c0002t0002g0091 others(2): Show |
7 | HG00438.hp1 HG00597.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.396+463_396+464ins others(22): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(17): Show |
1 | a0001c0002t0002g0140 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(24): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(19): Show |
1 | a0001c0002t0002g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(26): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(27): Show |
1 | a0001c0002t0020g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(34): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTAT others(33): Show |
1 | a0001c0002t0020g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(40): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTGT others(33): Show |
1 | a0001c0002t0006g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.396+463_396+464ins others(40): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300143 | G | GTGTGTGT others(35): Show |
1 | a0001c0002t0006g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.396+463_396+464ins others(42): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300143 | |||||||
chr14:20300145 | A | ATGTGTG | 2 | a0001c0002t0001g0056 a0001c0002t0003g0012 |
5 | HG02080.hp1 NA18951.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+461_396+462ins others(6): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300145 | |||||||
chr14:20300147 | A | G | 2 | a0001c0002t0001g0056 a0001c0002t0003g0012 |
5 | HG02080.hp1 NA18951.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+460T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300147 | |||||||
chr14:20300148 | T | C | 1 | a0001c0002t0014g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.396+459A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300148 | |||||||
chr14:20300155 | A | AT | 4 | a0001c0002t0002g0131 a0002c0003t0005g0026 a0002c0003t0005g0158 others(1): Show |
6 | HG02698.hp1 HG03225.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+451dupA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | ATATATAT others(20): Show |
1 | a0002c0004t0004g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.396+451_396+452ins others(27): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | ATATATAT others(36): Show |
1 | a0002c0004t0004g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.396+451_396+452ins others(43): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | ATATATAT others(25): Show |
1 | a0002c0003t0003g0157 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.396+451_396+452ins others(32): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | ATATATAT others(20): Show |
1 | a0002c0003t0003g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.396+451_396+452ins others(27): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | ATATATAT others(21): Show |
1 | a0002c0003t0031g0154 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.396+451_396+452ins others(28): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | A | T | 1 | a0002c0003t0005g0156 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.396+452T>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300155 | AT | A | 5 | a0001c0001t0001g0125 a0001c0002t0001g0056 a0001c0002t0003g0012 others(2): Show |
8 | HG02080.hp1 HG03041.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.396+451delA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300155 | |||||||
chr14:20300156 | T | TA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(101): Show |
235 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.396+450_396+451ins others(1): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA | 6 | a0001c0002t0009g0051 a0003c0006t0013g0053 a0003c0006t0013g0054 others(3): Show |
9 | HG01516.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.396+450_396+451ins others(7): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(6): Show |
1 | a0001c0002t0011g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.396+450_396+451ins others(13): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(8): Show |
1 | a0001c0002t0011g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.396+450_396+451ins others(15): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(14): Show |
1 | a0001c0007t0004g0011 | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.396+450_396+451ins others(21): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(16): Show |
1 | a0001c0002t0014g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.396+450_396+451ins others(23): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(18): Show |
1 | a0002c0003t0018g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.396+450_396+451ins others(25): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(20): Show |
1 | a0002c0003t0016g0192 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.396+450_396+451ins others(27): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(22): Show |
2 | a0002c0004t0004g0016 a0002c0004t0004g0040 |
2 | HG01069.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.396+450_396+451ins others(29): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(24): Show |
2 | a0002c0004t0004g0016 a0002c0004t0004g0040 |
3 | HG01496.hp1 NA18946.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.396+450_396+451ins others(31): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(26): Show |
1 | a0002c0004t0004g0016 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.396+450_396+451ins others(33): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(28): Show |
2 | a0002c0004t0004g0089 a0002c0004t0004g0090 |
2 | HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.396+450_396+451ins others(35): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(32): Show |
1 | a0001c0002t0009g0006 | 6 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+450_396+451ins others(39): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300156 | T | TATATATA others(40): Show |
1 | a0001c0002t0009g0006 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.396+450_396+451ins others(47): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300156 | |||||||
chr14:20300157 | T | A | 52 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0126 others(49): Show |
74 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.396+450A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300157 | |||||||
chr14:20300158 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(92): Show |
224 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.396+449A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300158 | |||||||
chr14:20300159 | T | A | 22 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0126 others(19): Show |
31 | HG00544.hp1 HG00558.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.396+448A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300159 | |||||||
chr14:20300160 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(85): Show |
210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.396+447A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300160 | |||||||
chr14:20300161 | T | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0126 others(18): Show |
30 | HG00544.hp1 HG00558.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.396+446A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300161 | |||||||
chr14:20300162 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(82): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.396+445A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300162 | |||||||
chr14:20300163 | T | A | 20 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0126 others(17): Show |
29 | HG00544.hp1 HG00558.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.396+444A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300163 | |||||||
chr14:20300164 | T | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(72): Show |
185 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.396+443A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300164 | |||||||
chr14:20300165 | T | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
11 | HG00544.hp1 HG03209.hp1 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.396+442A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300165 | |||||||
chr14:20300166 | T | A | 13 | a0001c0001t0001g0035 a0001c0001t0022g0049 a0001c0001t0026g0212 others(10): Show |
22 | HG01081.hp1 HG01109.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.396+441A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300166 | |||||||
chr14:20300167 | T | A | 2 | a0001c0001t0022g0214 a0001c0002t0056g0207 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.396+440A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300167 | |||||||
chr14:20300168 | T | A | 1 | a0001c0002t0003g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.396+439A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300168 | |||||||
chr14:20300169 | T | A | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.396+438A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300169 | |||||||
chr14:20300376 | T | C | 1 | a0001c0002t0002g0147 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.396+231A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300376 | |||||||
chr14:20300403 | C | T | 1 | a0001c0002t0003g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.396+204G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300403 | |||||||
chr14:20300479 | C | CTCCCTCC others(1): Show |
34 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(31): Show |
57 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.396+120_396+127dup others(8): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 3/9 | chr14 | 20300479 | |||||||
chr14:20300920 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.185-102C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20300920 | |||||||
chr14:20301135 | C | A | 42 | a0001c0001t0001g0076 a0001c0002t0001g0056 a0001c0002t0003g0012 others(39): Show |
59 | HG00323.hp2 HG00544.hp1 HG01358.hp2 others(56): Show |
intron_variant | MODIFIER | c.185-317G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20301135 | |||||||
chr14:20301297 | C | T | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-479G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20301297 | |||||||
chr14:20301558 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.184+275A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20301558 | |||||||
chr14:20301558 | T | C | 1 | a0001c0002t0002g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.184+275A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20301558 | |||||||
chr14:20301711 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(152): Show |
318 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.184+122C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 2/9 | chr14 | 20301711 | |||||||
chr14:20302034 | C | A | 1 | a0001c0002t0002g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.52-69G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302034 | |||||||
chr14:20302039 | C | T | 3 | a0001c0002t0002g0023 a0001c0002t0002g0036 a0001c0002t0002g0099 |
6 | HG02165.hp2 NA18966.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-74G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302039 | |||||||
chr14:20302165 | A | G | 1 | a0001c0002t0003g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.52-200T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302165 | |||||||
chr14:20302222 | G | A | 35 | a0001c0002t0001g0138 a0001c0002t0002g0004 a0001c0002t0002g0023 others(32): Show |
58 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.52-257C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302222 | |||||||
chr14:20302396 | T | A | 3 | a0001c0002t0020g0094 a0001c0002t0020g0095 a0001c0002t0044g0096 |
3 | HG02809.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52-431A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302396 | |||||||
chr14:20302455 | T | C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(1): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-490A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302455 | |||||||
chr14:20302534 | A | G | 1 | a0001c0002t0002g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.52-569T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302534 | |||||||
chr14:20302687 | T | C | 1 | a0001c0002t0002g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.52-722A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302687 | |||||||
chr14:20302768 | A | C | 1 | a0001c0001t0043g0098 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.52-803T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302768 | |||||||
chr14:20302777 | C | G | 5 | a0001c0002t0001g0056 a0001c0002t0003g0012 a0001c0002t0003g0028 others(2): Show |
9 | HG02027.hp1 HG02080.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-812G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302777 | |||||||
chr14:20302818 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.52-853G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302818 | |||||||
chr14:20302885 | AT | A | 5 | a0001c0001t0022g0049 a0001c0001t0022g0214 a0001c0002t0020g0094 others(2): Show |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-921delA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302885 | |||||||
chr14:20302897 | T | A | 2 | a0002c0003t0012g0204 a0002c0003t0012g0205 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.52-932A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302897 | |||||||
chr14:20302971 | G | C | 1 | a0003c0006t0013g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.52-1006C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302971 | |||||||
chr14:20302973 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(82): Show |
205 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.52-1008G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20302973 | |||||||
chr14:20303061 | G | A | 3 | a0001c0002t0020g0094 a0001c0002t0020g0095 a0001c0002t0044g0096 |
3 | HG02809.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52-1096C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303061 | |||||||
chr14:20303066 | C | A | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-1101G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303066 | |||||||
chr14:20303087 | G | A | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52-1122C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303087 | |||||||
chr14:20303185 | C | G | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1220G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303185 | |||||||
chr14:20303186 | G | C | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1221C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303186 | |||||||
chr14:20303189 | TCAAAAAA others(21): Show |
T | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1252_52-1225del others(28): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303189 | |||||||
chr14:20303190 | C | CA | 11 | a0001c0001t0001g0002 a0001c0001t0012g0021 a0001c0001t0022g0049 others(8): Show |
12 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.52-1226dupT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303190 | |||||||
chr14:20303231 | G | GAGGGAGT others(6): Show |
1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1267_52-1266ins others(13): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303231 | |||||||
chr14:20303238 | A | C | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1273T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303238 | |||||||
chr14:20303243 | T | C | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1278A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303243 | |||||||
chr14:20303244 | G | A | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1279C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303244 | |||||||
chr14:20303245 | A | G | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1280T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303245 | |||||||
chr14:20303246 | T | G | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1281A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303246 | |||||||
chr14:20303254 | A | G | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1289T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303254 | |||||||
chr14:20303257 | G | T | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1292C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303257 | |||||||
chr14:20303262 | C | T | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1297G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303262 | |||||||
chr14:20303263 | A | G | 1 | a0001c0001t0021g0097 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.52-1298T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303263 | |||||||
chr14:20303358 | T | C | 1 | a0001c0001t0006g0151 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.52-1393A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303358 | |||||||
chr14:20303399 | A | G | 3 | a0001c0002t0020g0094 a0001c0002t0020g0095 a0001c0002t0044g0096 |
3 | HG02809.hp2 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52-1434T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303399 | |||||||
chr14:20303409 | C | G | 2 | a0002c0003t0007g0152 a0002c0003t0007g0153 |
2 | HG01255.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.52-1444G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303409 | |||||||
chr14:20303483 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(84): Show |
213 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.52-1518A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303483 | |||||||
chr14:20303664 | TATAAAAA others(14): Show |
T | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-1720_52-1700del others(21): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303664 | |||||||
chr14:20303929 | C | T | 1 | a0001c0002t0002g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.51+1958G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20303929 | |||||||
chr14:20304010 | C | A | 1 | a0001c0002t0056g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.51+1877G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304010 | |||||||
chr14:20304010 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(82): Show |
205 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.51+1877G>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304010 | |||||||
chr14:20304022 | A | G | 1 | a0002c0004t0004g0092 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.51+1865T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304022 | |||||||
chr14:20304031 | T | A | 4 | a0001c0002t0008g0008 a0001c0002t0008g0048 a0001c0002t0008g0208 others(1): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+1856A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304031 | |||||||
chr14:20304257 | A | C | 1 | a0001c0002t0002g0091 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.51+1630T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304257 | |||||||
chr14:20304590 | CCTGCACC others(41): Show |
C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1249_51+1296del others(48): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304590 | |||||||
chr14:20304646 | C | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1241G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304646 | |||||||
chr14:20304651 | A | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1236T>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304651 | |||||||
chr14:20304670 | A | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1217T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304670 | |||||||
chr14:20304674 | A | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1213T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304674 | |||||||
chr14:20304678 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1209A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304678 | |||||||
chr14:20304679 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1208A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304679 | |||||||
chr14:20304684 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1203A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304684 | |||||||
chr14:20304688 | A | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1199T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304688 | |||||||
chr14:20304690 | A | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1197T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304690 | |||||||
chr14:20304691 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1196A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304691 | |||||||
chr14:20304696 | A | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1191T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304696 | |||||||
chr14:20304699 | A | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1188T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304699 | |||||||
chr14:20304702 | T | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1185A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304702 | |||||||
chr14:20304703 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1184A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304703 | |||||||
chr14:20304704 | C | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1183G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304704 | |||||||
chr14:20304705 | C | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1182G>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304705 | |||||||
chr14:20304706 | T | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1181A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304706 | |||||||
chr14:20304725 | T | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1162A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304725 | |||||||
chr14:20304729 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1158A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304729 | |||||||
chr14:20304739 | G | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1148C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304739 | |||||||
chr14:20304740 | A | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1147T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304740 | |||||||
chr14:20304743 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1144A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304743 | |||||||
chr14:20304744 | T | G | 44 | a0001c0001t0001g0076 a0001c0002t0001g0056 a0001c0002t0003g0012 others(41): Show |
67 | HG00323.hp2 HG00544.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.51+1143A>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304744 | |||||||
chr14:20304751 | A | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1136T>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304751 | |||||||
chr14:20304752 | G | T | 3 | a0002c0004t0004g0088 a0002c0004t0004g0089 a0002c0004t0004g0090 |
3 | HG02135.hp1 HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.51+1135C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304752 | |||||||
chr14:20304753 | G | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1134C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304753 | |||||||
chr14:20304754 | G | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1133C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304754 | |||||||
chr14:20304757 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1130A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304757 | |||||||
chr14:20304763 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1124A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304763 | |||||||
chr14:20304765 | G | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1122C>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304765 | |||||||
chr14:20304768 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1119A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304768 | |||||||
chr14:20304770 | T | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1117A>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304770 | |||||||
chr14:20304772 | G | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1115C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304772 | |||||||
chr14:20304773 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1114A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304773 | |||||||
chr14:20304778 | A | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1109T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304778 | |||||||
chr14:20304780 | A | T | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1107T>A | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304780 | |||||||
chr14:20304781 | C | G | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1106G>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304781 | |||||||
chr14:20304785 | A | AGGGTGGG others(21): Show |
1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1101_51+1102ins others(28): Show |
TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304785 | |||||||
chr14:20304787 | A | C | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1100T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304787 | |||||||
chr14:20304800 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1087A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304800 | |||||||
chr14:20304801 | T | A | 1 | a0001c0001t0006g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.51+1086A>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304801 | |||||||
chr14:20304874 | A | C | 42 | a0001c0001t0001g0076 a0001c0002t0001g0056 a0001c0002t0003g0012 others(39): Show |
59 | HG00323.hp2 HG00544.hp1 HG01358.hp2 others(56): Show |
intron_variant | MODIFIER | c.51+1013T>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304874 | |||||||
chr14:20304911 | T | TA | 5 | a0001c0001t0022g0049 a0001c0001t0022g0214 a0001c0001t0026g0212 others(2): Show |
6 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.51+975dupT | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304911 | |||||||
chr14:20304939 | A | G | 2 | a0003c0006t0013g0053 a0003c0006t0013g0054 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.51+948T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304939 | |||||||
chr14:20304973 | C | CT | 2 | a0001c0002t0009g0006 a0001c0002t0009g0051 |
8 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.51+913dupA | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20304973 | |||||||
chr14:20305181 | G | A | 1 | a0001c0001t0025g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.51+706C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20305181 | |||||||
chr14:20305413 | A | G | 1 | a0001c0002t0010g0050 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.51+474T>C | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20305413 | |||||||
chr14:20305418 | G | C | 1 | a0001c0007t0004g0011 | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+469C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20305418 | |||||||
chr14:20305444 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.51+443C>T | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20305444 | |||||||
chr14:20305532 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.51+355C>G | TTC5 | ENSG00000136319.12 | transcript | ENST00000258821.8 | protein_coding | 1/9 | chr14 | 20305532 |