Item | Value |
---|---|
geneid | 55773 |
ensemblid | ENSG00000036054.13 |
hgncid | 25622 |
symbol | TBC1D23 |
name | TBC1 domain family member 23 |
refseq_nuc | NM_001199198.3 |
refseq_prot | NP_001186127.1 |
ensembl_nuc | ENST00000394144.9 |
ensembl_prot | ENSP00000377700.4 |
mane_status | MANE Select |
chr | chr3 |
start | 100260992 |
end | 100325238 |
strand | + |
ver | v1.2 |
region | chr3:100260992-100325238 |
region5000 | chr3:100255992-100330238 |
regionname0 | TBC1D23_chr3_100260992_100325238 |
regionname5000 | TBC1D23_chr3_100255992_100330238 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 699 | 357 | 77 | 70 | 162 | 16 | 30 | 140 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | MAEGE others(694): Show |
chr3 | 100255992 | 100330238 |
a0002 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | MAEGE others(694): Show |
chr3 | 100255992 | 100330238 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2097 | 338 | 65 | 70 | 155 | 16 | 30 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0002 | 0/0 | 2097 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0003 | 0/0 | 2097 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0004 | 0/0 | 2097 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0005 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0007 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0001c0008 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 | ||
a0002c0006 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | ATGGC others(2092): Show |
chr3 | 100255992 | 100330238 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3697 | 269 | 43 | 48 | 147 | 10 | 21 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0002 | 1/0 | 3697 | 60 | 17 | 21 | 8 | 6 | 7 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0005 | 0/1 | 3697 | 2 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0006 | 0/0 | 3697 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0007 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0008 | 0/0 | 3697 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0001t0009 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0002t0003 | 0/0 | 3697 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0003t0001 | 0/0 | 3697 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0004t0004 | 0/0 | 3697 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0005t0010 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0007t0001 | 0/0 | 3697 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0001c0008t0002 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
a0002c0006t0001 | 0/0 | 3697 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | GGCAA others(3692): Show |
chr3 | 100255992 | 100330238 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0005g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0002t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0002t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0004t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0004t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0004t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0005t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0001c0008t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
a0002c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | FIN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0116 | EUR | FIN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | IBS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02572 | hp1 | a0001 | c0005 | t0010 | g0154 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02717 | hp1 | a0001 | c0008 | t0002 | g0139 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02818 | hp2 | a0002 | c0006 | t0001 | g0279 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02896 | hp1 | a0001 | c0004 | t0004 | g0165 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0093 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0169 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0132 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0121 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0092 | AFR | YRI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | CHB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18980 | hp1 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18987 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19043 | hp2 | a0001 | c0004 | t0004 | g0166 | AFR | LWK | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ASW | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | TSI | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | GIH | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0094 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | ACB | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
HG06807 | hp2 | a0001 | c0004 | t0004 | g0164 | AFR | USA | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | LWK | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0128 | REF | REF | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0202 | REF | REF | TBC1D23_chr3_100255992_100330238 | TBC1D23 | chr3 | 100255992 | 100330238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100304855 | G | A | 1 | a0002 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1273G>A | p.Glu425Lys | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/19 | 1300/3697 | 1273/2100 | 425/699 | chr3 | 100304855 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100283761 | C | G | 1 | a0001c0008 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.426C>G | p.Arg142Arg | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/19 | 453/3697 | 426/2100 | 142/699 | chr3 | 100283761 | |||
chr3:100295302 | A | G | 1 | a0001c0008 | 1 | HG02717.hp1 | splice_region_variant&synonymous_variant | LOW | c.726A>G | p.Lys242Lys | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/19 | 753/3697 | 726/2100 | 242/699 | chr3 | 100295302 | |||
chr3:100297988 | G | A | 1 | a0001c0005 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.942G>A | p.Gln314Gln | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/19 | 969/3697 | 942/2100 | 314/699 | chr3 | 100297988 | |||
chr3:100316141 | C | T | 1 | a0001c0007 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.1641C>T | p.Gly547Gly | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/19 | 1668/3697 | 1641/2100 | 547/699 | chr3 | 100316141 | |||
chr3:100320801 | T | C | 1 | a0001c0003 | 6 | NA18612.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
synonymous_variant | LOW | c.1848T>C | p.His616His | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/19 | 1875/3697 | 1848/2100 | 616/699 | chr3 | 100320801 | |||
chr3:100320966 | C | A | 1 | a0001c0004 | 3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.2013C>A | p.Ile671Ile | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/19 | 2040/3697 | 2013/2100 | 671/699 | chr3 | 100320966 | |||
chr3:100323623 | C | G | 1 | a0001c0002 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.2055C>G | p.Ala685Ala | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 2082/3697 | 2055/2100 | 685/699 | chr3 | 100323623 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100324005 | A | T | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(5): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 337 | chr3 | 100324005 | ||||||
chr3:100324136 | T | C | 1 | a0001c0001t0009 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*468T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 468 | chr3 | 100324136 | ||||||
chr3:100324445 | C | T | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(5): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*777C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 777 | chr3 | 100324445 | ||||||
chr3:100324488 | T | C | 1 | a0001c0005t0010 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 820 | chr3 | 100324488 | ||||||
chr3:100324502 | T | C | 1 | a0001c0001t0005 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*834T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 834 | chr3 | 100324502 | ||||||
chr3:100324588 | T | A | 1 | a0001c0001t0007 | 2 | HG02615.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*920T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 920 | chr3 | 100324588 | ||||||
chr3:100324669 | A | C | 1 | a0001c0004t0004 | 3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1001A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 1001 | chr3 | 100324669 | ||||||
chr3:100324990 | A | C | 1 | a0001c0001t0006 | 2 | HG03490.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1322A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 1322 | chr3 | 100324990 | ||||||
chr3:100325060 | T | C | 1 | a0001c0002t0003 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1392T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 1392 | chr3 | 100325060 | ||||||
chr3:100325101 | G | A | 1 | a0001c0001t0008 | 2 | HG02976.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1433G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 19/19 | 1433 | chr3 | 100325101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:100261099 | A | G | 1 | a0001c0001t0002g0310 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.53+28A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261099 | |||||||
chr3:100261178 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53+107G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261178 | |||||||
chr3:100261226 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.53+155G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261226 | |||||||
chr3:100261437 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
106 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.53+366T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261437 | |||||||
chr3:100261553 | T | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53+482T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261553 | |||||||
chr3:100261616 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53+545C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261616 | |||||||
chr3:100261637 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.53+566C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261637 | |||||||
chr3:100261666 | AG | A | 57 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.53+596delG | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261666 | |||||||
chr3:100261867 | T | A | 8 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+796T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261867 | |||||||
chr3:100261889 | T | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01168.hp1 HG01169.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.53+818T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100261889 | |||||||
chr3:100262116 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.53+1045G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262116 | |||||||
chr3:100262234 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
119 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.53+1163T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262234 | |||||||
chr3:100262303 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53+1232T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262303 | |||||||
chr3:100262475 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18947.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.53+1404A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262475 | |||||||
chr3:100262517 | G | C | 1 | a0001c0001t0002g0117 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53+1446G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262517 | |||||||
chr3:100262635 | GA | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.53+1566delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262635 | ||||||
chr3:100262723 | C | CA | 72 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0030 others(69): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.53+1674dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262723 | ||||||
chr3:100262723 | C | CAA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(104): Show |
127 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.53+1673_53+1674dup others(2): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262723 | ||||||
chr3:100262723 | C | CAAA | 30 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0038 others(27): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.53+1672_53+1674dup others(3): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262723 | ||||||
chr3:100262723 | C | CAAAA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0031 others(11): Show |
19 | HG00280.hp2 HG01071.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.53+1671_53+1674dup others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262723 | ||||||
chr3:100262723 | C | CAAAAA | 8 | a0001c0001t0001g0034 a0001c0001t0002g0118 a0001c0001t0002g0119 others(5): Show |
8 | HG00741.hp1 HG01106.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+1670_53+1674dup others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100262723 | ||||||
chr3:100262744 | A | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+1673A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262744 | |||||||
chr3:100262746 | C | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0123 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.53+1675C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262746 | |||||||
chr3:100262867 | T | G | 57 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.53+1796T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100262867 | |||||||
chr3:100263093 | C | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.53+2022C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263093 | |||||||
chr3:100263099 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.53+2028G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263099 | |||||||
chr3:100263195 | A | G | 1 | a0001c0003t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53+2124A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263195 | |||||||
chr3:100263246 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.53+2175G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263246 | |||||||
chr3:100263306 | A | G | 56 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(53): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+2235A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263306 | |||||||
chr3:100263608 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.53+2537A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263608 | |||||||
chr3:100263763 | C | T | 44 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.53+2692C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263763 | |||||||
chr3:100263795 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.53+2724G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263795 | |||||||
chr3:100263853 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01106.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53+2782A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100263853 | |||||||
chr3:100264022 | C | T | 1 | a0001c0001t0002g0137 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.53+2951C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100264022 | |||||||
chr3:100264267 | C | T | 57 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.53+3196C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100264267 | |||||||
chr3:100264503 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.53+3432T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100264503 | |||||||
chr3:100264852 | G | A | 14 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+3781G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100264852 | |||||||
chr3:100264961 | C | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG00280.hp1 HG01074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+3890C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100264961 | |||||||
chr3:100265023 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53+3952A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100265023 | |||||||
chr3:100265169 | G | GGT | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.53+4101_53+4102dup others(2): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100265169 | ||||||
chr3:100265408 | G | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.53+4337G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100265408 | |||||||
chr3:100265809 | C | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.53+4738C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100265809 | |||||||
chr3:100266025 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+4954A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100266025 | |||||||
chr3:100266040 | G | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(231): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.53+4969G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100266040 | |||||||
chr3:100266209 | CTTATT | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.53+5143_53+5147del others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100266209 | ||||||
chr3:100266332 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0264 |
2 | HG02293.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.53+5261G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100266332 | |||||||
chr3:100266335 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53+5264C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100266335 | |||||||
chr3:100266482 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0305 |
2 | HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.53+5411C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100266482 | |||||||
chr3:100267188 | A | C | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.53+6117A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267188 | |||||||
chr3:100267201 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.53+6130G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267201 | |||||||
chr3:100267637 | T | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.53+6566T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267637 | |||||||
chr3:100267662 | A | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.53+6591A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267662 | |||||||
chr3:100267741 | G | A | 2 | a0001c0004t0004g0164 a0001c0004t0004g0165 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.53+6670G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267741 | |||||||
chr3:100267775 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.53+6704A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267775 | |||||||
chr3:100267999 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.53+6928C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100267999 | |||||||
chr3:100268105 | G | A | 56 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(53): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.53+7034G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100268105 | |||||||
chr3:100268173 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0160 others(38): Show |
44 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.53+7102A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100268173 | |||||||
chr3:100268399 | A | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.53+7328A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100268399 | |||||||
chr3:100268517 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.53+7446A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100268517 | |||||||
chr3:100268839 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.53+7768G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100268839 | |||||||
chr3:100269026 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.53+7955G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269026 | |||||||
chr3:100269118 | A | G | 2 | a0001c0004t0004g0164 a0001c0004t0004g0165 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.53+8047A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269118 | |||||||
chr3:100269140 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.53+8069G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269140 | |||||||
chr3:100269142 | C | T | 1 | a0001c0004t0004g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.53+8071C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269142 | |||||||
chr3:100269162 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.53+8091A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269162 | |||||||
chr3:100269192 | CT | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.53+8123delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100269192 | ||||||
chr3:100269831 | T | C | 5 | a0001c0001t0008g0168 a0001c0001t0008g0169 a0001c0004t0004g0164 others(2): Show |
5 | HG02896.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+8760T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269831 | |||||||
chr3:100269978 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53+8907A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100269978 | |||||||
chr3:100270258 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.53+9187T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100270258 | |||||||
chr3:100270553 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-9096A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100270553 | |||||||
chr3:100271166 | G | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.54-8483G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271166 | |||||||
chr3:100271217 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-8432G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271217 | |||||||
chr3:100271259 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.54-8390A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271259 | |||||||
chr3:100271346 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.54-8303C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271346 | |||||||
chr3:100271392 | T | C | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.54-8257T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271392 | |||||||
chr3:100271489 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.54-8160G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271489 | |||||||
chr3:100271530 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.54-8119G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271530 | |||||||
chr3:100271538 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-8111A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271538 | |||||||
chr3:100271938 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.54-7711T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271938 | |||||||
chr3:100271984 | G | A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02132.hp2 NA18973.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-7665G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100271984 | |||||||
chr3:100272047 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(232): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.54-7602A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272047 | |||||||
chr3:100272242 | GAC | G | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-7405_54-7404del others(2): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100272242 | ||||||
chr3:100272639 | C | T | 2 | a0001c0001t0006g0121 a0001c0001t0006g0132 |
2 | HG03490.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.54-7010C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272639 | |||||||
chr3:100272710 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.54-6939G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272710 | |||||||
chr3:100272743 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.54-6906G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272743 | |||||||
chr3:100272850 | T | G | 1 | a0001c0001t0001g0266 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.54-6799T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272850 | |||||||
chr3:100272959 | A | G | 1 | a0001c0002t0003g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.54-6690A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272959 | |||||||
chr3:100272990 | G | A | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.54-6659G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100272990 | |||||||
chr3:100273126 | C | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.54-6523C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273126 | |||||||
chr3:100273221 | G | A | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-6428G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273221 | |||||||
chr3:100273303 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54-6346C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273303 | |||||||
chr3:100273325 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.54-6324A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273325 | |||||||
chr3:100273353 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0008g0168 a0001c0001t0008g0169 |
3 | HG02976.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.54-6296T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273353 | |||||||
chr3:100273359 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.54-6290T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273359 | |||||||
chr3:100273499 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.54-6150C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273499 | |||||||
chr3:100273501 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0252 |
3 | HG03041.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.54-6148C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273501 | |||||||
chr3:100273549 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-6100C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273549 | |||||||
chr3:100273648 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54-6001C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273648 | |||||||
chr3:100273681 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-5968A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273681 | |||||||
chr3:100273779 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0252 others(1): Show |
5 | HG02258.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-5870C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273779 | |||||||
chr3:100273789 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54-5860G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273789 | |||||||
chr3:100273836 | C | T | 57 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.54-5813C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273836 | |||||||
chr3:100273968 | G | A | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.54-5681G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100273968 | |||||||
chr3:100274069 | T | C | 2 | a0001c0004t0004g0164 a0001c0004t0004g0165 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.54-5580T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274069 | |||||||
chr3:100274114 | A | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.54-5535A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274114 | |||||||
chr3:100274255 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.54-5394T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274255 | |||||||
chr3:100274397 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54-5252G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274397 | |||||||
chr3:100274679 | A | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0118 a0001c0001t0002g0119 others(6): Show |
11 | HG00280.hp2 HG00741.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-4970A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274679 | |||||||
chr3:100274803 | T | C | 6 | a0001c0001t0001g0188 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG02135.hp1 NA18940.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-4846T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274803 | |||||||
chr3:100274808 | T | A | 1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54-4841T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274808 | |||||||
chr3:100274828 | CAT | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0218 |
5 | NA18961.hp2 NA18966.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-4815_54-4814del others(2): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100274828 | ||||||
chr3:100274881 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.54-4768G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274881 | |||||||
chr3:100274894 | A | AC | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
110 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.54-4746dupC | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100274894 | ||||||
chr3:100274904 | T | C | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG00099.hp1 HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.54-4745T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274904 | |||||||
chr3:100274906 | TTTG | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(59): Show |
67 | HG00140.hp1 HG00597.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.54-4740_54-4738del others(3): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100274906 | ||||||
chr3:100274934 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-4715C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100274934 | |||||||
chr3:100275038 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54-4611A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275038 | |||||||
chr3:100275254 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.54-4395T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275254 | |||||||
chr3:100275574 | C | T | 8 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0179 others(5): Show |
8 | HG00544.hp2 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-4075C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275574 | |||||||
chr3:100275616 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0189 others(3): Show |
10 | HG02165.hp1 NA18956.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-4033G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275616 | |||||||
chr3:100275697 | T | C | 1 | a0001c0001t0009g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54-3952T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275697 | |||||||
chr3:100275984 | G | A | 1 | a0001c0001t0009g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54-3665G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100275984 | |||||||
chr3:100276001 | G | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00544.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.54-3648G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276001 | |||||||
chr3:100276035 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0086 |
2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.54-3614G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276035 | |||||||
chr3:100276036 | A | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0086 |
2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.54-3613A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276036 | |||||||
chr3:100276086 | TA | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
120 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.54-3547delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100276086 | ||||||
chr3:100276277 | G | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.54-3372G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276277 | |||||||
chr3:100276572 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.54-3077T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276572 | |||||||
chr3:100276835 | G | T | 2 | a0001c0004t0004g0164 a0001c0004t0004g0165 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.54-2814G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100276835 | |||||||
chr3:100277086 | C | G | 56 | a0001c0001t0001g0145 a0001c0001t0002g0007 a0001c0001t0002g0008 others(53): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.54-2563C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277086 | |||||||
chr3:100277604 | A | T | 1 | a0001c0004t0004g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.54-2045A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277604 | |||||||
chr3:100277634 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
118 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.54-2015T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277634 | |||||||
chr3:100277667 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.54-1982A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277667 | |||||||
chr3:100277789 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54-1860C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277789 | |||||||
chr3:100277966 | A | G | 1 | a0001c0004t0004g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54-1683A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100277966 | |||||||
chr3:100278006 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.54-1643G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278006 | |||||||
chr3:100278080 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.54-1569C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278080 | |||||||
chr3:100278198 | C | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(231): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.54-1451C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278198 | |||||||
chr3:100278325 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00597.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.54-1324T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278325 | |||||||
chr3:100278366 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00544.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.54-1283A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278366 | |||||||
chr3:100278386 | A | AT | 18 | a0001c0001t0001g0084 a0001c0001t0001g0095 a0001c0001t0001g0172 others(15): Show |
18 | HG00099.hp1 HG00140.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-1246dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 100278386 | ||||||
chr3:100278520 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.54-1129G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278520 | |||||||
chr3:100278546 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54-1103C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278546 | |||||||
chr3:100278557 | T | A | 1 | a0001c0001t0001g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54-1092T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278557 | |||||||
chr3:100278574 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02523.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.54-1075C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100278574 | |||||||
chr3:100279455 | G | A | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0281 others(4): Show |
7 | HG00140.hp1 HG01358.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-194G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 1/18 | chr3 | 100279455 | |||||||
chr3:100280136 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.165+376A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280136 | |||||||
chr3:100280178 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.165+418G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280178 | |||||||
chr3:100280222 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+462C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280222 | |||||||
chr3:100280228 | C | CA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0170 others(4): Show |
8 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+478dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 100280228 | ||||||
chr3:100280332 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
118 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.165+572A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280332 | |||||||
chr3:100280576 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | NA18940.hp1 NA18945.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.165+816G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280576 | |||||||
chr3:100280952 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(23): Show |
33 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.166-790G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100280952 | |||||||
chr3:100281019 | G | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.166-723G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100281019 | |||||||
chr3:100281103 | A | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.166-639A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100281103 | |||||||
chr3:100281343 | C | A | 8 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
9 | NA18612.hp2 NA18950.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-399C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100281343 | |||||||
chr3:100281524 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-218T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 2/18 | chr3 | 100281524 | |||||||
chr3:100282185 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.271+338G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282185 | |||||||
chr3:100282189 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.271+342G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282189 | |||||||
chr3:100282199 | C | T | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.271+352C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282199 | |||||||
chr3:100282318 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.271+471C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282318 | |||||||
chr3:100282347 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.271+500C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282347 | |||||||
chr3:100282531 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00642.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.271+684T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282531 | |||||||
chr3:100282584 | G | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
304 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.271+737G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282584 | |||||||
chr3:100282786 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.272-821A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282786 | |||||||
chr3:100282908 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.272-699A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282908 | |||||||
chr3:100282909 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(23): Show |
33 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.272-698T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100282909 | |||||||
chr3:100283003 | G | A | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.272-604G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100283003 | |||||||
chr3:100283025 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.272-582A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100283025 | |||||||
chr3:100283146 | G | A | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.272-461G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100283146 | |||||||
chr3:100283539 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.272-68A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 3/18 | chr3 | 100283539 | |||||||
chr3:100283940 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.476+129C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100283940 | |||||||
chr3:100284160 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.476+349G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284160 | |||||||
chr3:100284177 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.476+366A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284177 | |||||||
chr3:100284289 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.476+478C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284289 | |||||||
chr3:100284354 | T | TTA | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0077 others(4): Show |
9 | HG00735.hp2 HG01168.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.476+552_476+553dup others(2): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 100284354 | ||||||
chr3:100284423 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.476+612C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284423 | |||||||
chr3:100284674 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.476+863G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284674 | |||||||
chr3:100284968 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.476+1157G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100284968 | |||||||
chr3:100285273 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.476+1462G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285273 | |||||||
chr3:100285435 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.476+1624A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285435 | |||||||
chr3:100285504 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.476+1693T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285504 | |||||||
chr3:100285651 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.476+1840C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285651 | |||||||
chr3:100285776 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.476+1965A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285776 | |||||||
chr3:100285813 | C | T | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG01928.hp1 HG01993.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+2002C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285813 | |||||||
chr3:100285826 | G | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.476+2015G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285826 | |||||||
chr3:100285994 | A | G | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.476+2183A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100285994 | |||||||
chr3:100286018 | A | G | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+2207A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286018 | |||||||
chr3:100286139 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0252 others(1): Show |
5 | HG02258.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.476+2328G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286139 | |||||||
chr3:100286274 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.476+2463A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286274 | |||||||
chr3:100286501 | C | CT | 7 | a0001c0001t0001g0201 a0001c0001t0002g0108 a0001c0001t0002g0109 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.476+2704dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 100286501 | ||||||
chr3:100286501 | CTT | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
107 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.476+2703_476+2704d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 100286501 | ||||||
chr3:100286591 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.476+2780G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286591 | |||||||
chr3:100286649 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.476+2838G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286649 | |||||||
chr3:100286820 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01106.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.476+3009A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286820 | |||||||
chr3:100286847 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00544.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.476+3036C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100286847 | |||||||
chr3:100287100 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.476+3289A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287100 | |||||||
chr3:100287123 | C | CT | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.476+3319dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 100287123 | ||||||
chr3:100287355 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0239 |
2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.477-3223A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287355 | |||||||
chr3:100287415 | G | A | 9 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0270 others(6): Show |
9 | HG00738.hp2 HG00741.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.477-3163G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287415 | |||||||
chr3:100287708 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.477-2870A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287708 | |||||||
chr3:100287852 | C | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(32): Show |
42 | HG00423.hp1 HG00609.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.477-2726C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287852 | |||||||
chr3:100287896 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.477-2682C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287896 | |||||||
chr3:100287905 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.477-2673C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100287905 | |||||||
chr3:100288049 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.477-2529C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288049 | |||||||
chr3:100288087 | T | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.477-2491T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288087 | |||||||
chr3:100288242 | T | TA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.477-2322dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 100288242 | ||||||
chr3:100288319 | C | G | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.477-2259C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288319 | |||||||
chr3:100288507 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0167 |
3 | HG02809.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.477-2071C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288507 | |||||||
chr3:100288562 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.477-2016A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288562 | |||||||
chr3:100288668 | C | A | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.477-1910C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288668 | |||||||
chr3:100288702 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477-1876A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288702 | |||||||
chr3:100288927 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.477-1651C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100288927 | |||||||
chr3:100289011 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.477-1567C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289011 | |||||||
chr3:100289046 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.477-1532T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289046 | |||||||
chr3:100289172 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0123 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-1406G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289172 | |||||||
chr3:100289238 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.477-1340C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289238 | |||||||
chr3:100289262 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.477-1316A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289262 | |||||||
chr3:100289295 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
112 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.477-1283A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289295 | |||||||
chr3:100289701 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.477-877A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289701 | |||||||
chr3:100289709 | T | C | 3 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0001g0266 |
3 | HG01346.hp2 HG01358.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.477-869T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289709 | |||||||
chr3:100289753 | T | G | 1 | a0001c0001t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.477-825T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289753 | |||||||
chr3:100289774 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
107 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.477-804G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289774 | |||||||
chr3:100289871 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.477-707A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100289871 | |||||||
chr3:100290033 | G | A | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.477-545G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100290033 | |||||||
chr3:100290102 | C | T | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.477-476C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100290102 | |||||||
chr3:100290254 | G | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.477-324G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100290254 | |||||||
chr3:100290558 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.477-20T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 4/18 | chr3 | 100290558 | |||||||
chr3:100290903 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.600+202A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100290903 | |||||||
chr3:100291271 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.600+570A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291271 | |||||||
chr3:100291364 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | NA18940.hp1 NA18945.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+663C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291364 | |||||||
chr3:100291582 | C | CA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
13 | HG01106.hp1 HG01346.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+897dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100291582 | ||||||
chr3:100291794 | T | TGC | 4 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02080.hp1 HG03139.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+1093_600+1094i others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291794 | |||||||
chr3:100291795 | T | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.600+1094T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291795 | |||||||
chr3:100291796 | C | CT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
104 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.600+1110dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100291796 | ||||||
chr3:100291796 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02080.hp1 HG03139.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+1095C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291796 | |||||||
chr3:100291902 | A | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0116 a0001c0001t0002g0134 others(6): Show |
11 | HG00323.hp2 HG01192.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.600+1201A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100291902 | |||||||
chr3:100292183 | G | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.600+1482G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292183 | |||||||
chr3:100292270 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+1569G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292270 | |||||||
chr3:100292329 | C | T | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.600+1628C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292329 | |||||||
chr3:100292398 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.600+1697T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292398 | |||||||
chr3:100292458 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(34): Show |
44 | HG00423.hp1 HG00609.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.600+1757C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292458 | |||||||
chr3:100292492 | A | G | 1 | a0001c0001t0009g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.600+1791A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292492 | |||||||
chr3:100292961 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.601-2126G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292961 | |||||||
chr3:100292982 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.601-2105G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100292982 | |||||||
chr3:100293009 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.601-2078C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293009 | |||||||
chr3:100293104 | A | AGTTT | 25 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(22): Show |
26 | HG00099.hp1 HG00597.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.601-1962_601-1959d others(6): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100293104 | ||||||
chr3:100293104 | A | AGTTTGTT others(1): Show |
119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(116): Show |
133 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.601-1966_601-1959d others(10): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100293104 | ||||||
chr3:100293104 | A | AGTTTGTT others(5): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0095 others(13): Show |
21 | HG00544.hp1 HG00597.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.601-1970_601-1959d others(14): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100293104 | ||||||
chr3:100293104 | A | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0167 a0001c0001t0001g0193 others(1): Show |
5 | HG02809.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-1983A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293104 | |||||||
chr3:100293130 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-1957C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293130 | |||||||
chr3:100293149 | ATTTT | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.601-1937_601-1934d others(6): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293149 | |||||||
chr3:100293161 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1926G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293161 | |||||||
chr3:100293282 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.601-1805C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293282 | |||||||
chr3:100293283 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.601-1804G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293283 | |||||||
chr3:100293331 | C | T | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-1756C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293331 | |||||||
chr3:100293443 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.601-1644T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293443 | |||||||
chr3:100293603 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1484A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293603 | |||||||
chr3:100293632 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0100 |
2 | NA18949.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.601-1455C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293632 | |||||||
chr3:100293992 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
118 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.601-1095G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100293992 | |||||||
chr3:100294027 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18947.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.601-1060C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294027 | |||||||
chr3:100294071 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.601-1016A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294071 | |||||||
chr3:100294150 | A | T | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-937A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294150 | |||||||
chr3:100294257 | T | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.601-830T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294257 | |||||||
chr3:100294265 | A | AT | 5 | a0001c0001t0001g0028 a0001c0001t0001g0193 a0001c0001t0001g0234 others(2): Show |
6 | HG03041.hp2 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-809dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 100294265 | ||||||
chr3:100294284 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.601-803A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294284 | |||||||
chr3:100294373 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.601-714G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294373 | |||||||
chr3:100294550 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.601-537T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294550 | |||||||
chr3:100294552 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.601-535C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100294552 | |||||||
chr3:100295044 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.601-43A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 5/18 | chr3 | 100295044 | |||||||
chr3:100295762 | G | A | 16 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(13): Show |
16 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.773-410G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100295762 | |||||||
chr3:100295799 | C | T | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.773-373C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100295799 | |||||||
chr3:100295837 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.773-335A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100295837 | |||||||
chr3:100295905 | A | C | 2 | a0001c0001t0002g0156 a0001c0001t0009g0155 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.773-267A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100295905 | |||||||
chr3:100295999 | A | G | 8 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0179 others(5): Show |
8 | HG00544.hp2 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.773-173A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100295999 | |||||||
chr3:100296005 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.773-167C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100296005 | |||||||
chr3:100296103 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.773-69C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 7/18 | chr3 | 100296103 | |||||||
chr3:100296302 | G | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.876+27G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296302 | |||||||
chr3:100296322 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
95 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.876+47C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296322 | |||||||
chr3:100296378 | T | C | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.876+103T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296378 | |||||||
chr3:100296381 | C | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.876+106C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296381 | |||||||
chr3:100296405 | AT | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(74): Show |
93 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.876+141delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100296405 | ||||||
chr3:100296644 | G | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.876+369G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296644 | |||||||
chr3:100296647 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0252 |
3 | HG03041.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.876+372C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296647 | |||||||
chr3:100296672 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.876+397A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296672 | |||||||
chr3:100296675 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.876+400C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296675 | |||||||
chr3:100296677 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.876+402G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296677 | |||||||
chr3:100296687 | A | G | 5 | a0001c0001t0002g0108 a0001c0001t0002g0110 a0001c0001t0002g0111 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+412A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296687 | |||||||
chr3:100296706 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01106.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.876+431A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296706 | |||||||
chr3:100296720 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.876+445C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296720 | |||||||
chr3:100296753 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG02257.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.876+478G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296753 | |||||||
chr3:100296777 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0023 others(38): Show |
49 | HG00423.hp1 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.876+502G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296777 | |||||||
chr3:100296860 | C | CA | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
115 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.876+604dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100296860 | ||||||
chr3:100296860 | CA | C | 11 | a0001c0001t0001g0191 a0001c0001t0001g0210 a0001c0001t0001g0227 others(8): Show |
11 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.876+604delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100296860 | ||||||
chr3:100296889 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0246 |
3 | NA19004.hp2 NA19009.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.876+614A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296889 | |||||||
chr3:100296999 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.876+724G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100296999 | |||||||
chr3:100297486 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.877-437A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100297486 | |||||||
chr3:100297634 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.877-289C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100297634 | |||||||
chr3:100297695 | G | GT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.877-218dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100297695 | ||||||
chr3:100297794 | ATTAAG | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-126_877-122del others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100297794 | ||||||
chr3:100297882 | A | AT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.877-31dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 100297882 | ||||||
chr3:100297907 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.877-16A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 8/18 | chr3 | 100297907 | |||||||
chr3:100298247 | A | G | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.999+202A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298247 | |||||||
chr3:100298293 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.999+248G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298293 | |||||||
chr3:100298303 | TC | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.999+260delC | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 100298303 | ||||||
chr3:100298327 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.999+282A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298327 | |||||||
chr3:100298397 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999+352A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298397 | |||||||
chr3:100298588 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.999+543C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298588 | |||||||
chr3:100298604 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | NA18940.hp1 NA18945.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.999+559G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298604 | |||||||
chr3:100298616 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.999+571C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298616 | |||||||
chr3:100298846 | C | T | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1000-393C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298846 | |||||||
chr3:100298879 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1000-360A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100298879 | |||||||
chr3:100299035 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1000-204A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 9/18 | chr3 | 100299035 | |||||||
chr3:100299375 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1092+44T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299375 | |||||||
chr3:100299391 | T | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+60T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299391 | |||||||
chr3:100299397 | T | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+66T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299397 | |||||||
chr3:100299498 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1092+167C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299498 | |||||||
chr3:100299539 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0179 a0001c0008t0002g0139 |
3 | HG00544.hp2 HG02717.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1092+208C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299539 | |||||||
chr3:100299592 | C | G | 1 | a0001c0004t0004g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1092+261C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299592 | |||||||
chr3:100299711 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1092+380A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299711 | |||||||
chr3:100299739 | G | T | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1092+408G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299739 | |||||||
chr3:100299871 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1092+540C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100299871 | |||||||
chr3:100299958 | ACT | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(83): Show |
105 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1092+632_1092+633d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100299958 | ||||||
chr3:100300280 | C | G | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1092+949C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100300280 | |||||||
chr3:100300298 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0008g0168 a0001c0001t0008g0169 |
3 | HG02976.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1092+967G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100300298 | |||||||
chr3:100300498 | A | AT | 70 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(67): Show |
75 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1092+1187dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100300498 | ||||||
chr3:100300498 | AT | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
100 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1092+1187delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100300498 | ||||||
chr3:100300498 | ATT | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0082 a0001c0002t0003g0092 others(3): Show |
6 | HG01993.hp1 HG02896.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+1186_1092+118 others(6): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100300498 | ||||||
chr3:100300596 | G | A | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1092+1265G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100300596 | |||||||
chr3:100300795 | C | T | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1093-1272C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100300795 | |||||||
chr3:100300838 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0252 others(1): Show |
5 | HG02258.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-1229C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100300838 | |||||||
chr3:100301272 | C | CA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
120 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1093-776dupA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100301272 | ||||||
chr3:100301272 | C | CAA | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(134): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1093-777_1093-776d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100301272 | ||||||
chr3:100301272 | C | CAAA | 18 | a0001c0001t0001g0091 a0001c0001t0001g0253 a0001c0001t0001g0254 others(15): Show |
18 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1093-778_1093-776d others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 100301272 | ||||||
chr3:100301692 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1093-375A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100301692 | |||||||
chr3:100301797 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG00280.hp1 HG01074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-270C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100301797 | |||||||
chr3:100301867 | A | T | 1 | a0001c0001t0002g0133 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1093-200A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100301867 | |||||||
chr3:100301888 | A | G | 2 | a0001c0001t0001g0277 a0002c0006t0001g0279 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1093-179A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 10/18 | chr3 | 100301888 | |||||||
chr3:100302521 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1263+284G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302521 | |||||||
chr3:100302638 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1263+401G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302638 | |||||||
chr3:100302711 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1263+474C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302711 | |||||||
chr3:100302714 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01106.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1263+477G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302714 | |||||||
chr3:100302814 | C | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1263+577C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302814 | |||||||
chr3:100302831 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1263+594G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302831 | |||||||
chr3:100302894 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0002c0006t0001g0279 |
3 | HG02572.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1263+657G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100302894 | |||||||
chr3:100303386 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1263+1149A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100303386 | |||||||
chr3:100303573 | C | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264-1273C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100303573 | |||||||
chr3:100303686 | G | A | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1264-1160G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100303686 | |||||||
chr3:100303781 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1264-1065T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100303781 | |||||||
chr3:100303813 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0224 others(3): Show |
7 | NA18946.hp2 NA18947.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264-1033G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100303813 | |||||||
chr3:100304083 | TGATGTCT others(5): Show |
T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1264-761_1264-750d others(14): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 100304083 | ||||||
chr3:100304218 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1264-628G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100304218 | |||||||
chr3:100304480 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1264-366A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 11/18 | chr3 | 100304480 | |||||||
chr3:100305089 | T | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
95 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1306+201T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305089 | |||||||
chr3:100305277 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+389T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305277 | |||||||
chr3:100305428 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00642.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1306+540G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305428 | |||||||
chr3:100305460 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1306+572T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305460 | |||||||
chr3:100305564 | A | G | 1 | a0001c0001t0002g0020 | 2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1306+676A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305564 | |||||||
chr3:100305709 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1307-728A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100305709 | |||||||
chr3:100306181 | A | G | 1 | a0001c0004t0004g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1307-256A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100306181 | |||||||
chr3:100306324 | C | A | 1 | a0001c0001t0007g0029 | 2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1307-113C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 12/18 | chr3 | 100306324 | |||||||
chr3:100306766 | GC | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
104 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1413+224delC | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100306766 | |||||||
chr3:100307276 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1413+733T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100307276 | |||||||
chr3:100307840 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0218 a0001c0001t0001g0299 |
6 | HG03942.hp2 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+1297T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100307840 | |||||||
chr3:100308119 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1413+1576G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308119 | |||||||
chr3:100308204 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
118 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1413+1661A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308204 | |||||||
chr3:100308303 | G | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1413+1760G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308303 | |||||||
chr3:100308431 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1413+1888C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308431 | |||||||
chr3:100308450 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1413+1907C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308450 | |||||||
chr3:100308529 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | HG01106.hp1 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1414-1874A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308529 | |||||||
chr3:100308590 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1414-1813A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308590 | |||||||
chr3:100308652 | G | C | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1414-1751G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308652 | |||||||
chr3:100308801 | ACTTC | A | 17 | a0001c0001t0002g0009 a0001c0001t0002g0116 a0001c0001t0002g0117 others(14): Show |
19 | HG00323.hp2 HG01192.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1414-1597_1414-159 others(8): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100308801 | ||||||
chr3:100308877 | C | T | 4 | a0001c0001t0002g0108 a0001c0001t0002g0110 a0001c0001t0002g0111 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-1526C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100308877 | |||||||
chr3:100309105 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1414-1298C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309105 | |||||||
chr3:100309194 | C | CAA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1414-1208_1414-120 others(6): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309194 | ||||||
chr3:100309356 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0096 a0001c0001t0001g0099 |
3 | HG00280.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1414-1047A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309356 | |||||||
chr3:100309610 | C | CTT | 13 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(10): Show |
13 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1414-775_1414-774d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTT | 34 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0162 others(31): Show |
36 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1414-778_1414-774d others(7): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTT | 16 | a0001c0001t0001g0047 a0001c0001t0001g0084 a0001c0001t0001g0160 others(13): Show |
16 | HG00738.hp1 HG00738.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1414-779_1414-774d others(8): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTTT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(63): Show |
81 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1414-780_1414-774d others(9): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTTT others(1): Show |
25 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0035 others(22): Show |
27 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1414-781_1414-774d others(10): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0170 |
3 | HG00735.hp1 HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1414-786_1414-774d others(15): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0171 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1414-787_1414-774d others(16): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1414-788_1414-774d others(17): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309610 | CTTTTTT | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0040 others(6): Show |
13 | HG00609.hp2 HG01167.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1414-779_1414-774d others(8): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309610 | ||||||
chr3:100309642 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1414-761C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309642 | |||||||
chr3:100309653 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1414-750G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309653 | |||||||
chr3:100309686 | A | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-717A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309686 | |||||||
chr3:100309692 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1414-711A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309692 | |||||||
chr3:100309705 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1414-698A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309705 | |||||||
chr3:100309772 | G | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(2): Show |
5 | HG01106.hp1 HG02257.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-631G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309772 | |||||||
chr3:100309827 | T | TC | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
91 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1414-575dupC | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 100309827 | ||||||
chr3:100309853 | C | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-550C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309853 | |||||||
chr3:100309854 | C | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-549C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309854 | |||||||
chr3:100309855 | T | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-548T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309855 | |||||||
chr3:100309857 | C | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-546C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309857 | |||||||
chr3:100309858 | C | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-545C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309858 | |||||||
chr3:100309859 | T | C | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-544T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309859 | |||||||
chr3:100309860 | C | A | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1414-543C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309860 | |||||||
chr3:100309980 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1414-423A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309980 | |||||||
chr3:100309990 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1414-413G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100309990 | |||||||
chr3:100310001 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1414-402T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100310001 | |||||||
chr3:100310050 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1414-353G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100310050 | |||||||
chr3:100310329 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1414-74A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 13/18 | chr3 | 100310329 | |||||||
chr3:100310647 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1553+105G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100310647 | |||||||
chr3:100310705 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1553+163T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100310705 | |||||||
chr3:100310707 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1553+165T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100310707 | |||||||
chr3:100310781 | C | T | 8 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1553+239C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100310781 | |||||||
chr3:100311026 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1553+484A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100311026 | |||||||
chr3:100311102 | A | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1553+560A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100311102 | |||||||
chr3:100311168 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0123 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1553+626C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100311168 | |||||||
chr3:100311303 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA18942.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1554-530G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100311303 | |||||||
chr3:100311693 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02135.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1554-140T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | chr3 | 100311693 | |||||||
chr3:100311784 | A | AT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(77): Show |
96 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1554-41dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 100311784 | ||||||
chr3:100311920 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1598+43C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100311920 | |||||||
chr3:100311943 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1598+66A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100311943 | |||||||
chr3:100312125 | T | G | 1 | a0001c0008t0002g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1598+248T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312125 | |||||||
chr3:100312239 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1598+362C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312239 | |||||||
chr3:100312283 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1598+406C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312283 | |||||||
chr3:100312296 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1598+419A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312296 | |||||||
chr3:100312357 | T | G | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1598+480T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312357 | |||||||
chr3:100312465 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1598+588A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312465 | |||||||
chr3:100312572 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1598+695A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312572 | |||||||
chr3:100312630 | C | G | 5 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0123 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1598+753C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312630 | |||||||
chr3:100312724 | GA | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(24): Show |
34 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.1598+856delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100312724 | ||||||
chr3:100312795 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1598+918C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312795 | |||||||
chr3:100312867 | C | T | 14 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1598+990C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312867 | |||||||
chr3:100312876 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1598+999G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312876 | |||||||
chr3:100312879 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1598+1002C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312879 | |||||||
chr3:100312880 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1598+1003G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100312880 | |||||||
chr3:100313001 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0060 |
2 | HG02004.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1598+1124C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313001 | |||||||
chr3:100313004 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1598+1127C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313004 | |||||||
chr3:100313010 | A | AAAT | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
97 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1598+1153_1598+115 others(7): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100313010 | ||||||
chr3:100313010 | A | AAATAAT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0062 others(6): Show |
10 | HG02080.hp1 HG02976.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1598+1150_1598+115 others(10): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100313010 | ||||||
chr3:100313033 | T | A | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1598+1156T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313033 | |||||||
chr3:100313034 | A | T | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1598+1157A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313034 | |||||||
chr3:100313625 | T | G | 2 | a0001c0004t0004g0164 a0001c0004t0004g0165 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1598+1748T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313625 | |||||||
chr3:100313656 | G | A | 1 | a0001c0001t0001g0011 | 2 | NA18969.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1598+1779G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313656 | |||||||
chr3:100313733 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1598+1856C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313733 | |||||||
chr3:100313924 | TA | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
95 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1598+2051delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100313924 | ||||||
chr3:100313958 | C | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0096 a0001c0001t0001g0098 others(1): Show |
4 | HG00280.hp1 HG02735.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1598+2081C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100313958 | |||||||
chr3:100314017 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18956.hp1 NA19076.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1599-2082T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314017 | |||||||
chr3:100314041 | TTGAGGAA others(17): Show |
T | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1599-2056_1599-203 others(28): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100314041 | ||||||
chr3:100314091 | A | AT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1599-1983dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100314091 | ||||||
chr3:100314091 | A | ATT | 24 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0038 others(21): Show |
25 | HG00609.hp2 HG01243.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1599-1984_1599-198 others(6): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100314091 | ||||||
chr3:100314091 | A | ATTT | 7 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0261 others(4): Show |
7 | HG00642.hp2 HG00733.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1599-1985_1599-198 others(7): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100314091 | ||||||
chr3:100314091 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1599-1993_1599-198 others(15): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100314091 | ||||||
chr3:100314133 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1599-1966C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314133 | |||||||
chr3:100314159 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1599-1940C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314159 | |||||||
chr3:100314212 | T | C | 5 | a0001c0001t0002g0117 a0001c0001t0002g0135 a0001c0001t0002g0140 others(2): Show |
5 | NA18961.hp1 NA18964.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1599-1887T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314212 | |||||||
chr3:100314273 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(46): Show |
56 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1599-1826A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314273 | |||||||
chr3:100314295 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1599-1804A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314295 | |||||||
chr3:100314425 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
118 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1599-1674A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314425 | |||||||
chr3:100314625 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18947.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1599-1474C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314625 | |||||||
chr3:100314759 | C | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1599-1340C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100314759 | |||||||
chr3:100315088 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1599-1011A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315088 | |||||||
chr3:100315154 | C | CT | 6 | a0001c0001t0001g0174 a0001c0001t0001g0287 a0001c0001t0001g0292 others(3): Show |
6 | HG02055.hp2 HG02135.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1599-920dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CT | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1599-920delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTT | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(53): Show |
71 | HG00609.hp2 HG00735.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1599-921_1599-920d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTTT | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0081 others(7): Show |
10 | HG01496.hp1 HG01975.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1599-922_1599-920d others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1599-929_1599-920d others(12): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0082 a0001c0001t0001g0087 |
3 | HG00323.hp1 HG00733.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1599-931_1599-920d others(14): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1599-933_1599-920d others(16): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315154 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0071 |
3 | HG01496.hp2 HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1599-934_1599-920d others(17): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 100315154 | ||||||
chr3:100315242 | A | G | 2 | a0001c0001t0002g0156 a0001c0001t0009g0155 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1599-857A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315242 | |||||||
chr3:100315364 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1599-735G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315364 | |||||||
chr3:100315387 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1599-712C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315387 | |||||||
chr3:100315451 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1599-648C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315451 | |||||||
chr3:100315466 | C | G | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1599-633C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315466 | |||||||
chr3:100315681 | T | C | 1 | a0001c0005t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1599-418T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315681 | |||||||
chr3:100315800 | G | T | 5 | a0001c0002t0003g0012 a0001c0002t0003g0019 a0001c0002t0003g0092 others(2): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1599-299G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315800 | |||||||
chr3:100315877 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1599-222T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315877 | |||||||
chr3:100315896 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1599-203A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100315896 | |||||||
chr3:100316005 | A | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1599-94A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 15/18 | chr3 | 100316005 | |||||||
chr3:100316192 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00544.hp2 NA19066.hp1 |
splice_region_variant&intron_variant | LOW | c.1687+5A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316192 | |||||||
chr3:100316269 | C | G | 2 | a0001c0001t0002g0137 a0001c0001t0002g0142 |
2 | NA19005.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1687+82C>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316269 | |||||||
chr3:100316300 | A | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1687+113A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316300 | |||||||
chr3:100316469 | T | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0060 a0001c0001t0001g0067 others(2): Show |
5 | HG01167.hp1 HG02004.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687+282T>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316469 | |||||||
chr3:100316728 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1687+541A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316728 | |||||||
chr3:100316826 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1687+639T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100316826 | |||||||
chr3:100317081 | CA | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1687+911delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 100317081 | ||||||
chr3:100317109 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1687+922G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100317109 | |||||||
chr3:100317242 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00544.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1687+1055A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100317242 | |||||||
chr3:100317583 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1687+1396C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100317583 | |||||||
chr3:100317700 | A | ACTCT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1688-1366_1688-136 others(8): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 100317700 | ||||||
chr3:100317709 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1688-1360A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100317709 | |||||||
chr3:100317928 | TTTTATAT others(3): Show |
T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1688-1126_1688-111 others(14): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 100317928 | ||||||
chr3:100318045 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1688-1024G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318045 | |||||||
chr3:100318110 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-959G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318110 | |||||||
chr3:100318163 | G | A | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00544.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1688-906G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318163 | |||||||
chr3:100318369 | AAGC | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0122 a0001c0001t0002g0123 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1688-695_1688-693d others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 100318369 | ||||||
chr3:100318646 | CT | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0099 a0001c0001t0001g0242 others(3): Show |
6 | HG01109.hp2 HG01515.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1688-408delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr3 | 100318646 | ||||||
chr3:100318687 | G | T | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1688-382G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318687 | |||||||
chr3:100318800 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
216 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1688-269A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318800 | |||||||
chr3:100318827 | T | C | 19 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(16): Show |
19 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1688-242T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318827 | |||||||
chr3:100318951 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1688-118G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 16/18 | chr3 | 100318951 | |||||||
chr3:100319384 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
103 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1823+180T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319384 | |||||||
chr3:100319430 | C | CT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
106 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1823+235dupT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 100319430 | ||||||
chr3:100319461 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0252 |
3 | HG03041.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1823+257T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319461 | |||||||
chr3:100319535 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1823+331T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319535 | |||||||
chr3:100319564 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1823+360G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319564 | |||||||
chr3:100319582 | C | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
103 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1823+378C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319582 | |||||||
chr3:100319788 | T | G | 1 | a0001c0001t0001g0288 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+584T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319788 | |||||||
chr3:100319814 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1823+610C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319814 | |||||||
chr3:100319856 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1823+652C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100319856 | |||||||
chr3:100320073 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1824-704G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100320073 | |||||||
chr3:100320174 | C | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG00280.hp1 HG01074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824-603C>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100320174 | |||||||
chr3:100320222 | CGTATT | C | 8 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0179 others(5): Show |
8 | HG00544.hp2 HG02055.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1824-549_1824-545d others(7): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 100320222 | ||||||
chr3:100320223 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1824-554G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100320223 | |||||||
chr3:100320493 | ATATAT | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824-280_1824-276d others(7): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 100320493 | ||||||
chr3:100320753 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824-24T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 17/18 | chr3 | 100320753 | |||||||
chr3:100321164 | G | C | 1 | a0001c0001t0002g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2018+193G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321164 | |||||||
chr3:100321214 | T | C | 2 | a0001c0001t0008g0168 a0001c0001t0008g0169 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2018+243T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321214 | |||||||
chr3:100321308 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2018+337G>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321308 | |||||||
chr3:100321389 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2018+418C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321389 | |||||||
chr3:100321493 | T | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2018+522T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321493 | |||||||
chr3:100321546 | A | T | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2018+575A>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321546 | |||||||
chr3:100321666 | A | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2018+695A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321666 | |||||||
chr3:100321684 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0167 |
3 | HG02809.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2018+713T>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321684 | |||||||
chr3:100321710 | A | G | 3 | a0001c0004t0004g0164 a0001c0004t0004g0165 a0001c0004t0004g0166 |
3 | HG02896.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2018+739A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321710 | |||||||
chr3:100321830 | T | TAA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
99 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.2018+872_2018+873d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100321830 | ||||||
chr3:100321830 | T | TAAA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0046 others(4): Show |
8 | HG02027.hp2 HG04184.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.2018+871_2018+873d others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100321830 | ||||||
chr3:100321830 | TA | T | 64 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(61): Show |
69 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2018+873delA | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100321830 | ||||||
chr3:100321910 | AAT | A | 65 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2018+942_2018+943d others(4): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100321910 | ||||||
chr3:100321929 | CTGT | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2018+960_2018+962d others(5): Show |
TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100321929 | ||||||
chr3:100321975 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2018+1004A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100321975 | |||||||
chr3:100322108 | AT | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2018+1144delT | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 100322108 | ||||||
chr3:100322453 | A | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0082 |
2 | HG00733.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2019-1134A>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100322453 | |||||||
chr3:100322759 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2019-828G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100322759 | |||||||
chr3:100322859 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
113 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2019-728T>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100322859 | |||||||
chr3:100322894 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2019-693C>T | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100322894 | |||||||
chr3:100323036 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2019-551A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100323036 | |||||||
chr3:100323055 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2019-532G>C | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100323055 | |||||||
chr3:100323392 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-195G>A | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100323392 | |||||||
chr3:100323547 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0309 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2019-40A>G | TBC1D23 | ENSG00000036054.13 | transcript | ENST00000394144.9 | protein_coding | 18/18 | chr3 | 100323547 |